Substances and drugs that lower the SURFACE TENSION of the mucoid layer lining the PULMONARY ALVEOLI.
An abundant pulmonary surfactant-associated protein that binds to a variety of lung pathogens and enhances their opsinization and killing by phagocytic cells. Surfactant protein D contains a N-terminal collagen-like domain and a C-terminal lectin domain that are characteristic of members of the collectin family of proteins.
Proteins found in the LUNG that act as PULMONARY SURFACTANTS.
An abundant pulmonary surfactant-associated protein that binds to a variety of lung pathogens, resulting in their opsinization. It also stimulates MACROPHAGES to undergo PHAGOCYTOSIS of microorganisms. Surfactant protein A contains a N-terminal collagen-like domain and a C-terminal lectin domain that are characteristic of members of the collectin family of proteins.
Protein-lipid combinations abundant in brain tissue, but also present in a wide variety of animal and plant tissues. In contrast to lipoproteins, they are insoluble in water, but soluble in a chloroform-methanol mixture. The protein moiety has a high content of hydrophobic amino acids. The associated lipids consist of a mixture of GLYCEROPHOSPHATES; CEREBROSIDES; and SULFOGLYCOSPHINGOLIPIDS; while lipoproteins contain PHOSPHOLIPIDS; CHOLESTEROL; and TRIGLYCERIDES.
The force acting on the surface of a liquid, tending to minimize the area of the surface. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)
A pulmonary surfactant associated-protein that plays an essential role in alveolar stability by lowering the surface tension at the air-liquid interface. Inherited deficiency of pulmonary surfactant-associated protein B is one cause of RESPIRATORY DISTRESS SYNDROME, NEWBORN.
A pulmonary surfactant associated protein that plays a role in alveolar stability by lowering the surface tension at the air-liquid interface. It is a membrane-bound protein that constitutes 1-2% of the pulmonary surfactant mass. Pulmonary surfactant-associated protein C is one of the most hydrophobic peptides yet isolated and contains an alpha-helical domain with a central poly-valine segment that binds to phospholipid bilayers.
Synthetic phospholipid used in liposomes and lipid bilayers to study biological membranes. It is also a major constituent of PULMONARY SURFACTANTS.
A nitrogen-free class of lipids present in animal and particularly plant tissues and composed of one mole of glycerol and 1 or 2 moles of phosphatidic acid. Members of this group differ from one another in the nature of the fatty acids released on hydrolysis.
Agents that modify interfacial tension of water; usually substances that have one lipophilic and one hydrophilic group in the molecule; includes soaps, detergents, emulsifiers, dispersing and wetting agents, and several groups of antiseptics.
Either of the pair of organs occupying the cavity of the thorax that effect the aeration of the blood.
Small polyhedral outpouchings along the walls of the alveolar sacs, alveolar ducts and terminal bronchioles through the walls of which gas exchange between alveolar air and pulmonary capillary blood takes place.
Lipids containing one or more phosphate groups, particularly those derived from either glycerol (phosphoglycerides see GLYCEROPHOSPHOLIPIDS) or sphingosine (SPHINGOLIPIDS). They are polar lipids that are of great importance for the structure and function of cell membranes and are the most abundant of membrane lipids, although not stored in large amounts in the system.
The mixture of gases present in the earth's atmosphere consisting of oxygen, nitrogen, carbon dioxide, and small amounts of other gases.
The adhesion of gases, liquids, or dissolved solids onto a surface. It includes adsorptive phenomena of bacteria and viruses onto surfaces as well. ABSORPTION into the substance may follow but not necessarily.
Characteristics or attributes of the outer boundaries of objects, including molecules.
A condition of the newborn marked by DYSPNEA with CYANOSIS, heralded by such prodromal signs as dilatation of the alae nasi, expiratory grunt, and retraction of the suprasternal notch or costal margins, mostly frequently occurring in premature infants, children of diabetic mothers, and infants delivered by cesarean section, and sometimes with no apparent predisposing cause.
Washing liquid obtained from irrigation of the lung, including the BRONCHI and the PULMONARY ALVEOLI. It is generally used to assess biochemical, inflammatory, or infection status of the lung.
Complex pharmaceutical substances, preparations, or matter derived from organisms usually obtained by biological methods or assay.
Derivatives of phosphatidic acids in which the phosphoric acid is bound in ester linkage to a choline moiety. Complete hydrolysis yields 1 mole of glycerol, phosphoric acid and choline and 2 moles of fatty acids.
A class of C-type lectins that target the carbohydrate structures found on invading pathogens. Binding of collectins to microorganisms results in their agglutination and enhanced clearance. Collectins form trimers that may assemble into larger oligomers. Each collectin polypeptide chain consists of four regions: a relatively short N-terminal region, a collagen-like region, an alpha-helical coiled-coil region, and carbohydrate-binding region.
Round, granular, mononuclear phagocytes found in the alveoli of the lungs. They ingest small inhaled particles resulting in degradation and presentation of the antigen to immunocompetent cells.
Conjugated protein-carbohydrate compounds including mucins, mucoid, and amyloid glycoproteins.
The protein components of a number of complexes, such as enzymes (APOENZYMES), ferritin (APOFERRITINS), or lipoproteins (APOLIPOPROTEINS).
Artificially produced membranes, such as semipermeable membranes used in artificial kidney dialysis (RENAL DIALYSIS), monomolecular and bimolecular membranes used as models to simulate biological CELL MEMBRANES. These membranes are also used in the process of GUIDED TISSUE REGENERATION.
An unctuous substance composed of sebum and desquamated epithelial cells, which covers the skin of the fetus.
An immunoglobulin which accounts for less than 1% of plasma immunoglobulin. It is found on the membrane of many circulating B LYMPHOCYTES.
A PULMONARY ALVEOLI-filling disease, characterized by dense phospholipoproteinaceous deposits in the alveoli, cough, and DYSPNEA. This disease is often related to, congenital or acquired, impaired processing of PULMONARY SURFACTANTS by alveolar macrophages, a process dependent on GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR.
Domesticated bovine animals of the genus Bos, usually kept on a farm or ranch and used for the production of meat or dairy products or for heavy labor.
A type of stress exerted uniformly in all directions. Its measure is the force exerted per unit area. (McGraw-Hill Dictionary of Scientific and Technical Terms, 6th ed)
Epithelial cells that line the PULMONARY ALVEOLI.
The capability of the LUNGS to distend under pressure as measured by pulmonary volume change per unit pressure change. While not a complete description of the pressure-volume properties of the lung, it is nevertheless useful in practice as a measure of the comparative stiffness of the lung. (From Best & Taylor's Physiological Basis of Medical Practice, 12th ed, p562)
The thick green-to-black mucilaginous material found in the intestines of a full-term fetus. It consists of secretions of the INTESTINAL GLANDS; BILE PIGMENTS; FATTY ACIDS; AMNIOTIC FLUID; and intrauterine debris. It constitutes the first stools passed by a newborn.
Any of various animals that constitute the family Suidae and comprise stout-bodied, short-legged omnivorous mammals with thick skin, usually covered with coarse bristles, a rather long mobile snout, and small tail. Included are the genera Babyrousa, Phacochoerus (wart hogs), and Sus, the latter containing the domestic pig (see SUS SCROFA).
A benzofuran derivative used as a protein reagent since the terminal N-NBD-protein conjugate possesses interesting fluorescence and spectral properties. It has also been used as a covalent inhibitor of both beef heart mitochondrial ATPase and bacterial ATPase.
A clear, odorless, tasteless liquid that is essential for most animal and plant life and is an excellent solvent for many substances. The chemical formula is hydrogen oxide (H2O). (McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed)
Pathological processes involving any part of the LUNG.
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
All blood proteins except albumin ( = SERUM ALBUMIN, which is not a globulin) and FIBRINOGEN (which is not in the serum). The serum globulins are subdivided into ALPHA-GLOBULINS; BETA-GLOBULINS; and GAMMA-GLOBULINS on the basis of their electrophoretic mobilities. (From Dorland, 28th ed)
A clear, yellowish liquid that envelopes the FETUS inside the sac of AMNION. In the first trimester, it is likely a transudate of maternal or fetal plasma. In the second trimester, amniotic fluid derives primarily from fetal lung and kidney. Cells or substances in this fluid can be removed for prenatal diagnostic tests (AMNIOCENTESIS).
Layers of lipid molecules which are two molecules thick. Bilayer systems are frequently studied as models of biological membranes.
The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION.
Salts and esters of the 12-carbon saturated monocarboxylic acid--lauric acid.
A syndrome characterized by progressive life-threatening RESPIRATORY INSUFFICIENCY in the absence of known LUNG DISEASES, usually following a systemic insult such as surgery or major TRAUMA.
A generic term for fats and lipoids, the alcohol-ether-soluble constituents of protoplasm, which are insoluble in water. They comprise the fats, fatty oils, essential oils, waxes, phospholipids, glycolipids, sulfolipids, aminolipids, chromolipids (lipochromes), and fatty acids. (Grant & Hackh's Chemical Dictionary, 5th ed)
Functional competence of specific organs or body systems of the FETUS in utero.
A respiratory distress syndrome in newborn infants, usually premature infants with insufficient PULMONARY SURFACTANTS. The disease is characterized by the formation of a HYALINE-like membrane lining the terminal respiratory airspaces (PULMONARY ALVEOLI) and subsequent collapse of the lung (PULMONARY ATELECTASIS).
A type of scanning probe microscopy in which a probe systematically rides across the surface of a sample being scanned in a raster pattern. The vertical position is recorded as a spring attached to the probe rises and falls in response to peaks and valleys on the surface. These deflections produce a topographic map of the sample.
Inhaling liquid or solids, such as stomach contents, into the RESPIRATORY TRACT. When this causes severe lung damage, it is called ASPIRATION PNEUMONIA.
The unborn young of a viviparous mammal, in the postembryonic period, after the major structures have been outlined. In humans, the unborn young from the end of the eighth week after CONCEPTION until BIRTH, as distinguished from the earlier EMBRYO, MAMMALIAN.
The species Oryctolagus cuniculus, in the family Leporidae, order LAGOMORPHA. Rabbits are born in burrows, furless, and with eyes and ears closed. In contrast with HARES, rabbits have 22 chromosome pairs.
Washing out of the lungs with saline or mucolytic agents for diagnostic or therapeutic purposes. It is very useful in the diagnosis of diffuse pulmonary infiltrates in immunosuppressed patients.
Quartz (SiO2). A glassy or crystalline form of silicon dioxide. Many colored varieties are semiprecious stones. (From Grant & Hackh's Chemical Dictionary, 5th ed)
A change of a substance from one form or state to another.
The physical characteristics and processes of biological systems.
A naphthalene derivative with carcinogenic action.
Proteins prepared by recombinant DNA technology.
The study of PHYSICAL PHENOMENA and PHYSICAL PROCESSES as applied to living things.
The process in which substances, either endogenous or exogenous, bind to proteins, peptides, enzymes, protein precursors, or allied compounds. Specific protein-binding measures are often used as assays in diagnostic assessments.
The property of objects that determines the direction of heat flow when they are placed in direct thermal contact. The temperature is the energy of microscopic motions (vibrational and translational) of the particles of atoms.
The clumping together of suspended material resulting from the action of AGGLUTININS.
Nanometer-sized tubes composed mainly of CARBON. Such nanotubes are used as probes for high-resolution structural and chemical imaging of biomolecules with ATOMIC FORCE MICROSCOPY.
An infant during the first month after birth.
Cetyltrimethylammonium compounds that have cationic detergent, antiseptic, and disinfectant activities. They are used in pharmaceuticals, foods, and cosmetics as preservatives; on skin, mucous membranes, etc., as antiseptics or cleansers, and also as emulsifiers. These compounds are toxic when used orally due to neuromuscular blockade.
A strain of albino rat used widely for experimental purposes because of its calmness and ease of handling. It was developed by the Sprague-Dawley Animal Company.
Artificial, single or multilaminar vesicles (made from lecithins or other lipids) that are used for the delivery of a variety of biological molecules or molecular complexes to cells, for example, drug delivery and gene transfer. They are also used to study membranes and membrane proteins.
Differential thermal analysis in which the sample compartment of the apparatus is a differential calorimeter, allowing an exact measure of the heat of transition independent of the specific heat, thermal conductivity, and other variables of the sample.
A plant genus of the family POACEAE that contains the Phl p 4 allergen.
Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others.
Porphobilinogen is a porphyrin precursor, specifically the organic compound intermediate in the biosynthesis of heme and chlorophyll, formed by the condensation of two pyrrole molecules in the liver and other tissues.
RNA sequences that serve as templates for protein synthesis. Bacterial mRNAs are generally primary transcripts in that they do not require post-transcriptional processing. Eukaryotic mRNA is synthesized in the nucleus and must be exported to the cytoplasm for translation. Most eukaryotic mRNAs have a sequence of polyadenylic acid at the 3' end, referred to as the poly(A) tail. The function of this tail is not known for certain, but it may play a role in the export of mature mRNA from the nucleus as well as in helping stabilize some mRNA molecules by retarding their degradation in the cytoplasm.
Microscopy using an electron beam, instead of light, to visualize the sample, thereby allowing much greater magnification. The interactions of ELECTRONS with specimens are used to provide information about the fine structure of that specimen. In TRANSMISSION ELECTRON MICROSCOPY the reactions of the electrons that are transmitted through the specimen are imaged. In SCANNING ELECTRON MICROSCOPY an electron beam falls at a non-normal angle on the specimen and the image is derived from the reactions occurring above the plane of the specimen.
A common saturated fatty acid found in fats and waxes including olive oil, palm oil, and body lipids.
Particles consisting of aggregates of molecules held loosely together by secondary bonds. The surface of micelles are usually comprised of amphiphatic compounds that are oriented in a way that minimizes the energy of interaction between the micelle and its environment. Liquids that contain large numbers of suspended micelles are referred to as EMULSIONS.
The engulfing and degradation of microorganisms; other cells that are dead, dying, or pathogenic; and foreign particles by phagocytic cells (PHAGOCYTES).
The mucous membrane lining the RESPIRATORY TRACT, including the NASAL CAVITY; the LARYNX; the TRACHEA; and the BRONCHI tree. The respiratory mucosa consists of various types of epithelial cells ranging from ciliated columnar to simple squamous, mucous GOBLET CELLS, and glands containing both mucous and serous cells.
Any of the ruminant mammals with curved horns in the genus Ovis, family Bovidae. They possess lachrymal grooves and interdigital glands, which are absent in GOATS.
Electrophoresis in which a polyacrylamide gel is used as the diffusion medium.
Elements of limited time intervals, contributing to particular results or situations.
The rate dynamics in chemical or physical systems.
Proteins that share the common characteristic of binding to carbohydrates. Some ANTIBODIES and carbohydrate-metabolizing proteins (ENZYMES) also bind to carbohydrates, however they are not considered lectins. PLANT LECTINS are carbohydrate-binding proteins that have been primarily identified by their hemagglutinating activity (HEMAGGLUTININS). However, a variety of lectins occur in animal species where they serve diverse array of functions through specific carbohydrate recognition.
The sequence of PURINES and PYRIMIDINES in nucleic acids and polynucleotides. It is also called nucleotide sequence.
Microscopy of specimens stained with fluorescent dye (usually fluorescein isothiocyanate) or of naturally fluorescent materials, which emit light when exposed to ultraviolet or blue light. Immunofluorescence microscopy utilizes antibodies that are labeled with fluorescent dye.
Members of the class of compounds composed of AMINO ACIDS joined together by peptide bonds between adjacent amino acids into linear, branched or cyclical structures. OLIGOPEPTIDES are composed of approximately 2-12 amino acids. Polypeptides are composed of approximately 13 or more amino acids. PROTEINS are linear polypeptides that are normally synthesized on RIBOSOMES.
The exchange of OXYGEN and CARBON DIOXIDE between alveolar air and pulmonary capillary blood that occurs across the BLOOD-AIR BARRIER.
The study of CHEMICAL PHENOMENA and processes in terms of the underlying PHYSICAL PHENOMENA and processes.
The innermost membranous sac that surrounds and protects the developing embryo which is bathed in the AMNIOTIC FLUID. Amnion cells are secretory EPITHELIAL CELLS and contribute to the amniotic fluid.
A species of SWINE, in the family Suidae, comprising a number of subspecies including the domestic pig Sus scrofa domestica.
The thermodynamic interaction between a substance and WATER.
A large multisubunit protein complex found in the THYLAKOID MEMBRANE. It uses light energy derived from LIGHT-HARVESTING PROTEIN COMPLEXES to catalyze the splitting of WATER into DIOXYGEN and of reducing equivalents of HYDROGEN.
The motion of phospholipid molecules within the lipid bilayer, dependent on the classes of phospholipids present, their fatty acid composition and degree of unsaturation of the acyl chains, the cholesterol concentration, and temperature.
The principal sterol of all higher animals, distributed in body tissues, especially the brain and spinal cord, and in animal fats and oils.
A species of gram-negative, facultatively anaerobic, rod-shaped bacteria normally commensal in the flora of CATTLE and SHEEP. But under conditions of physical or PHYSIOLOGICAL STRESS, it can cause MASTITIS in sheep and SHIPPING FEVER or ENZOOTIC CALF PNEUMONIA in cattle. Its former name was Pasteurella haemolytica.
The level of protein structure in which regular hydrogen-bond interactions within contiguous stretches of polypeptide chain give rise to alpha helices, beta strands (which align to form beta sheets) or other types of coils. This is the first folding level of protein conformation.
Lipid-containing polysaccharides which are endotoxins and important group-specific antigens. They are often derived from the cell wall of gram-negative bacteria and induce immunoglobulin secretion. The lipopolysaccharide molecule consists of three parts: LIPID A, core polysaccharide, and O-specific chains (O ANTIGENS). When derived from Escherichia coli, lipopolysaccharides serve as polyclonal B-cell mitogens commonly used in laboratory immunology. (From Dorland, 28th ed)
A steroid-inducible protein that was originally identified in uterine fluid. It is a secreted homodimeric protein with identical 70-amino acid subunits that are joined in an antiparallel orientation by two disulfide bridges. A variety of activities are associated with uteroglobin including the sequestering of hydrophobic ligands and the inhibition of SECRETORY PHOSPHOLIPASE A2.
An anti-inflammatory 9-fluoro-glucocorticoid.
Usually high-molecular-weight, straight-chain primary alcohols, but can also range from as few as 4 carbons, derived from natural fats and oils, including lauryl, stearyl, oleyl, and linoleyl alcohols. They are used in pharmaceuticals, cosmetics, detergents, plastics, and lube oils and in textile manufacture. (From McGraw-Hill Dictionary of Scientific and Technical Terms, 5th ed)

Surfactant protein A enhances the binding and deacylation of E. coli LPS by alveolar macrophages. (1/423)

Surfactant protein (SP) A and SP-D are involved in multiple immunomodulatory functions of innate host defense partly via their interaction with alveolar macrophages (AMs). In addition, both SP-A and SP-D bind to bacterial lipopolysaccharide (LPS). To investigate the functional significance of this interaction, we first tested the ability of SP-A and SP-D to enhance the binding of tritium-labeled Escherichia coli LPS to AMs. In contrast to SP-D, SP-A enhanced the binding of LPS by AMs in a time-, temperature-, and concentration-dependent manner. Coincubation with surfactant-like lipids did not affect the SP-A-mediated enhancement of LPS binding. At SP-A-to-LPS molar ratios of 1:2-1:3, the LPS binding by AMs reached 270% of control values. Second, we investigated the role of SP-A in regulating the degradation of LPS by AMs. In the presence of SP-A, deacylation of LPS by AMs increased by approximately 2.3-fold. Pretreatment of AMs with phosphatidylinositol-specific phospholipase C had no effect on the SP-A-enhanced LPS binding but did reduce the amount of serum-enhanced LPS binding by 50%, suggesting that a cell surface molecule distinct from CD14 mediates the effect of SP-A. Together the results for the first time provide direct evidence that SP-A enhances LPS binding and degradation by AMs.  (+info)

Effects of endotoxin on surfactant protein A and D stimulation of NO production by alveolar macrophages. (2/423)

Surfactant protein (SP) A and SP-D affect numerous functions of immune cells including enhancing phagocytosis of bacteria and production of reactive species. Previous studies have shown that SP-A and SP-D bind to a variety of bacteria and to the lipopolysaccharide (LPS) components of their cell walls. In addition, purified preparations of SPs often contain endotoxin. The goals of this study were 1) to evaluate the effects of SP-A and SP-D and complexes of SPs and LPS on the production of nitric oxide metabolites by rat alveolar macrophages and 2) to evaluate methods for the removal of endotoxin with optimal recovery of SP. Incubation of SP-A or SP-D with polymyxin, 100 mM N-octyl-beta-D-glucopyranoside, and 2 mM EDTA followed by dialysis was the most effective method of those tested for reducing endotoxin levels. Commonly used storage buffers for SP-D, but not for SP-A, inhibited the detection of endotoxin. There was a correlation between the endotoxin content of the SP-A and SP-D preparations and their ability to stimulate production of nitrite by alveolar macrophages. SP-A and SP-D treated as described above to remove endotoxin did not stimulate nitrite production. These studies suggest that the functions of SP-A and SP-D are affected by endotoxin and illustrate the importance of monitoring SP preparations for endotoxin contamination.  (+info)

Surfactant protein D binds to Mycobacterium tuberculosis bacilli and lipoarabinomannan via carbohydrate-lectin interactions resulting in reduced phagocytosis of the bacteria by macrophages. (3/423)

Surfactant protein-D (SP-D) is a collectin produced in the distal lung airspaces that is believed to play an important role in innate pulmonary immunity. Naive immunologic responses to Mycobacterium tuberculosis (M.tb) are especially important in the lung, since entry of this inhaled pathogen into the alveolar macrophage is a pivotal event in disease pathogenesis. Here we investigated SP-D binding to M.tb and the effect of this binding on the adherence of M. tb to human macrophages. These studies demonstrate specific binding of SP-D to M.tb that is saturable, calcium dependent, and carbohydrate inhibitable. In addition to purified SP-D, SP-D in bronchoalveolar lavage fluids from healthy donors and patients with alveolar proteinosis also binds to M.tb. Incubation of M.tb with SP-D results in agglutination of the bacteria. In contrast to its binding to M.tb, SP-D binds minimally to the avirulent Mycobacterium smegmatis. SP-D binds predominantly to lipoarabinomannan from the virulent Erdman strain of M.tb, but not the lipoarabinomannan from M. smegmatis. The binding of SP-D to Erdman lipoarabinomannan is mediated by the terminal mannosyl oligosaccharides of this lipoglycan. Incubation of M.tb with subagglutinating concentrations of SP-D leads to reduced adherence of the bacteria to macrophages (62.7% of control adherence +/- 3.3% SEM, n = 8), whereas incubation of bacteria with surfactant protein A leads to significantly increased adherence to monocyte-derived macrophages. These data provide evidence for specific binding of SP-D to M. tuberculosis and indicate that SP-D and surfactant protein A serve different roles in the innate host response to this pathogen in the lung.  (+info)

Surfactant protein A and D expression in the porcine Eustachian tube. (4/423)

Surfactant proteins A and D are collectins which are considered to play an important role in the innate immunity of lungs. Our aim was to investigate whether surfactant protein A or D is expressed in the porcine Eustachian tube originating from the upper airways. Both surfactant proteins A and D were present in the epithelial cells of the Eustachian tube, as shown by strong immunostaining. Using RT-PCR and Northern hybridization, these collectins were detected in the Eustachian tube. The present study is the first report demonstrating surfactant protein gene expression in the Eustachian tube. Surfactant proteins A and D may be important in the antibody-independent protection of the middle ear.  (+info)

Aerosolized endotoxin is immediately bound by pulmonary surfactant protein D in vivo. (5/423)

Collectins are carbohydrate binding proteins that are implicated in innate host defense. The lung collectins, surfactant proteins A and D (SP-A and SP-D), bind a variety of pathogens in vitro and influence phagocytosis by alveolar macrophages. In this report we show that SP-D binds endotoxin (lipopolysaccharide, LPS) in vivo in a rat model of acute respiratory distress syndrome (ARDS). Intratracheal aerosolization of LPS in rats resulted in the typical features of human ARDS. Total amounts of SP-D, as well as the carbohydrate binding properties of SP-D were measured in lung lavage as a function of time. The amount of SP-D did not change during 24 h. Interestingly, SP-D in lung lavage isolated from rats during the first 2 h after LPS treatment, was not able to bind to carbohydrate. Further analysis revealed that the carbohydrate binding sites of SP-D were occupied by LPS, suggesting that SP-D is an LPS scavenging molecule in vivo. Electron microscopic analysis indicated that, 1 h after LPS aerosolization, aggregates of SP-D with LPS were found in lysosomal structures in alveolar macrophages. We conclude that the lung collectin SP-D binds inhaled endotoxin in vivo, which may help to protect the lung from endotoxin-induced disease.  (+info)

Binding of rat and human surfactant proteins A and D to Aspergillus fumigatus conidia. (6/423)

Surfactant proteins A (SP-A) and D (SP-D) are thought to play important roles in pulmonary host defense. We investigated the interactions of rat and human SP-A and SP-D with Aspergillus fumigatus conidia. Rat SP-D but not rat SP-A bound the conidia, and the binding was inhibited by EDTA, mannose, glucose, maltose, and inositol. Binding studies using a mutant recombinant rat SP-D with altered carbohydrate recognition but normal structural organization clearly established a role for the carbohydrate recognition domain in binding to conidia. However, neither rat SP-A nor SP-D increased the association of fluorescein isothiocyanate-labeled conidia with rat alveolar macrophages as determined by flow cytometry. Both human SP-A (isolated from normal and alveolar proteinosis lungs) and SP-D (recombinant protein and protein isolated from alveolar proteinosis lungs) bound the conidia. These data indicate that important differences exist between rat and human SP-A in binding to certain fungi. Human SP-A and SP-D binding to conidia was also examined in the presence of hydrophobic surfactant components (HSC), containing both the phospholipid and hydrophobic proteins of surfactant. We found that HSC inhibited but did not eliminate human SP-A binding to Aspergillus conidia. In contrast, the SP-D binding to conidia was unaffected by HSC. These findings indicate that SP-D plays a major role in the recognition of Aspergillus conidia in alveolar fluid.  (+info)

Cloning of gp-340, a putative opsonin receptor for lung surfactant protein D. (7/423)

Surfactant protein D (SP-D) is an oligomeric C type lectin that promotes phagocytosis by binding to microbial surface carbohydrates. A 340-kDa glycoprotein (gp-340) has been shown to bind SP-D in the presence of calcium but does so independently of carbohydrate recognition. This protein exists both in a soluble form and in association with the membranes of alveolar macrophages. The primary structure of gp-340 has been established by molecular cloning, which yielded a 7,686-bp cDNA sequence encoding a polypeptide chain of 2, 413 amino acids. The domain organization features 13 scavenger receptor cysteine-rich (SRCR) domains, each separated by an SRCR-interspersed domain, except for SRCRs 4 and 5, which are contiguous. The 13 SRCR domains are followed by two C1r/C1s Uegf Bmp1 domains separated by a 14th SRCR domain and a zona pellucida domain. gp-340 seems to be an alternative spliced form of DMBT1. Reverse transcription-PCR analysis showed that the main sites of synthesis of gp-340 are lung, trachea, salivary gland, small intestine, and stomach. Immunohistochemistry revealed strong staining for gp-340 in alveolar and other tissue macrophages. Immunostaining of the macrophage membrane was either uniform or focal in a way that suggested capping, whereas other macrophages showed strong intracellular staining within the phagosome/phagolysosome compartments. In some macrophages, SP-D and gp-340 were located in the same cellular compartment. Immunoreactive gp-340 was also found in epithelial cells of the small intestine and in the ducts of salivary glands. The distribution of gp-340 in macrophages is compatible with a role as an opsonin receptor for SP-D.  (+info)

Structural characterization of human and bovine lung surfactant protein D. (8/423)

Human and bovine surfactant proteins D (SP-D) were purified from late amniotic fluid and bronchioalveolar lavage on the basis of its Ca(2+)-dependent affinity for maltose. The molecular mass of a trimeric subunit was determined by matrix-assisted laser desorption ionization MS to lie in the range 115-125 kDa for human SP-D and 110-123 kDa for bovine SP-D. A single polypeptide chain was determined at 37-41 and 36-40 kDa for the human and bovine species respectively. The major parts of the primary structures of both SP-D molecules were determined by a combination of MS and Edman degradation. The heterogeneity in SP-D was caused mainly by a high number of post-translational modifications in the collagen-like region. Proline and lysine residues were partly hydroxylated and lysine residues were further O-glycosylated with the disaccharide galactose-glucose. A partly occupied N-linked glycosylation site was characterized in human SP-D. The carbohydrate was determined as a complex type bi-antennary structure, with a small content of mono-antennary and tri-antennary structures. No sialic acid residues were present on the glycan, but some had an attached fucose and/or an N-acetylglucosamine residue linked to the core. Bovine SP-D was determined as having a similar structure.  (+info)

Pulmonary surfactants are a complex mixture of lipids and proteins that are produced by the alveolar type II cells in the lungs. They play a crucial role in reducing the surface tension at the air-liquid interface within the alveoli, which helps to prevent collapse of the lungs during expiration. Surfactants also have important immunological functions, such as inhibiting the growth of certain bacteria and modulating the immune response. Deficiency or dysfunction of pulmonary surfactants can lead to respiratory distress syndrome (RDS) in premature infants and other lung diseases.

Pulmonary Surfactant-Associated Protein D, also known as SP-D or surfactant protein D, is a protein that belongs to the collectin family. It is produced by specialized cells called type II alveolar epithelial cells and is found in the lungs, where it plays an important role in maintaining lung homeostasis and host defense.

SP-D has several functions in the lungs, including:

1. Reducing surface tension: SP-D helps to reduce surface tension in the alveoli, which facilitates breathing by preventing the collapse of the lungs during expiration.
2. Host defense: SP-D plays a crucial role in innate immunity by recognizing and binding to pathogens such as bacteria, viruses, and fungi. This helps to neutralize and clear these microorganisms from the lungs.
3. Inflammation regulation: SP-D has anti-inflammatory properties and can help to regulate the immune response in the lungs. It does this by modulating the activation of immune cells such as macrophages and neutrophils.
4. Tissue repair: SP-D may also play a role in tissue repair and remodeling in the lungs, although its exact mechanisms are not fully understood.

Abnormalities in SP-D have been implicated in several lung diseases, including respiratory distress syndrome, asthma, chronic obstructive pulmonary disease (COPD), and interstitial lung diseases.

Pulmonary surfactant-associated proteins are a group of proteins that are found in the pulmonary surfactant, a complex mixture of lipids and proteins that coats the inside surfaces of the alveoli in the lungs. The primary function of pulmonary surfactant is to reduce the surface tension at the air-liquid interface in the alveoli, which facilitates breathing by preventing collapse of the alveoli during expiration.

There are four main pulmonary surfactant-associated proteins, designated as SP-A, SP-B, SP-C, and SP-D. These proteins play important roles in maintaining the stability and function of the pulmonary surfactant film, as well as participating in host defense mechanisms in the lungs.

SP-A and SP-D are members of the collectin family of proteins and have been shown to have immunomodulatory functions, including binding to pathogens and modulating immune cell responses. SP-B and SP-C are hydrophobic proteins that play critical roles in reducing surface tension at the air-liquid interface and maintaining the stability of the surfactant film.

Deficiencies or dysfunction of pulmonary surfactant-associated proteins have been implicated in various lung diseases, including respiratory distress syndrome (RDS) in premature infants, chronic interstitial lung diseases, and pulmonary fibrosis.

Pulmonary Surfactant-Associated Protein A (SP-A) is a protein that is a major component of pulmonary surfactant, which is a complex mixture of lipids and proteins found in the alveoli of the lungs. SP-A is produced by specialized cells called type II alveolar epithelial cells and has several important functions in the lung.

SP-A plays a role in innate immunity by binding to pathogens, such as bacteria and viruses, and facilitating their clearance from the lungs. It also helps to regulate surfactant homeostasis by participating in the reuptake and recycling of surfactant components. Additionally, SP-A has been shown to have anti-inflammatory effects and may help to modulate the immune response in the lung.

Deficiencies or mutations in SP-A have been associated with various respiratory diseases, including acute respiratory distress syndrome (ARDS), pulmonary fibrosis, and chronic obstructive pulmonary disease (COPD).

Proteolipids are a type of complex lipid-containing proteins that are insoluble in water and have a high content of hydrophobic amino acids. They are primarily found in the plasma membrane of cells, where they play important roles in maintaining the structural integrity and function of the membrane. Proteolipids are also found in various organelles, including mitochondria, lysosomes, and peroxisomes.

Proteolipids are composed of a hydrophobic protein core that is tightly associated with a lipid bilayer through non-covalent interactions. The protein component of proteolipids typically contains several transmembrane domains that span the lipid bilayer, as well as hydrophilic regions that face the cytoplasm or the lumen of organelles.

Proteolipids have been implicated in various cellular processes, including signal transduction, membrane trafficking, and ion transport. They are also associated with several neurological disorders, such as Alzheimer's disease, Parkinson's disease, and multiple sclerosis. The study of proteolipids is an active area of research in biochemistry and cell biology, with potential implications for the development of new therapies for neurological disorders.

Surface tension is not a term that has a specific medical definition. However, it is a physical chemistry concept that relates to the cohesive force between liquid molecules, causing the surface of the liquid to contract and have a higher intermolecular force than its bulk.

In a broader sense, surface tension can have implications in certain medical or biological contexts, such as the movement of liquids in the lungs or the stability of lipid bilayers in cell membranes. But it is not a term that is typically used to describe medical conditions or treatments.

Pulmonary Surfactant-Associated Protein B (SP-B) is a small, hydrophobic protein that is an essential component of pulmonary surfactant. Surfactant is a complex mixture of lipids and proteins that reduces surface tension at the air-liquid interface in the alveoli of the lungs, thereby preventing collapse of the alveoli during expiration and facilitating lung expansion during inspiration. SP-B plays a crucial role in the biophysical function of surfactant by promoting its spreading and stability. It is synthesized and processed within type II alveolar epithelial cells and secreted as a part of lamellar bodies, which are lipoprotein complexes that store and release surfactant. Deficiency or dysfunction of SP-B can lead to severe respiratory distress syndrome (RDS) in infants and other lung diseases in both children and adults.

Pulmonary surfactant-associated protein C (SP-C) is a small hydrophobic protein that is a component of pulmonary surfactant. Surfactant is a complex mixture of lipids and proteins that reduces surface tension in the alveoli of the lungs, preventing collapse during expiration and facilitating lung expansion during inspiration. SP-C plays a crucial role in maintaining the structural integrity and stability of the surfactant film at the air-liquid interface of the alveoli.

Deficiency or dysfunction of SP-C has been associated with several pulmonary diseases, including respiratory distress syndrome (RDS) in premature infants, interstitial lung diseases (ILDs), and pulmonary fibrosis. Mutations in the gene encoding SP-C (SFTPC) can lead to abnormal protein processing and accumulation, resulting in lung injury and inflammation, ultimately contributing to the development of these conditions.

1,2-Dipalmitoylphosphatidylcholine (DPPC) is a type of phospholipid molecule that is a major component of the lipid bilayer in biological membranes, particularly in lung surfactant. It is composed of two palmitic acid chains attached to a glycerol backbone, which is linked to a phosphate group and a choline headgroup. The chemical formula for DPPC is C44H86NO8P.

In the body, DPPC plays an important role in maintaining the structure and function of cell membranes, as well as reducing surface tension in the lungs. It is also used in research and medical settings as a component of liposomes, which are used for drug delivery and other biomedical applications.

Phosphatidylglycerols are a type of glycerophospholipids, which are major components of biological membranes. They are composed of a glycerol backbone to which two fatty acid chains and a phosphate group are attached. In the case of phosphatidylglycerols, the phosphate group is linked to a glycerol molecule through an ester bond, forming a phosphoglyceride.

Phosphatidylglycerols are unique because they have an additional glycerol molecule attached to the phosphate group, making them more complex than other glycerophospholipids such as phosphatidylcholine or phosphatidylethanolamine. This additional glycerol moiety can be further modified by the addition of various headgroups, leading to the formation of different subclasses of phosphatidylglycerols.

In biological membranes, phosphatidylglycerols are often found in the inner leaflet of the mitochondrial membrane and play important roles in maintaining the structure and function of this organelle. They have also been implicated in various cellular processes such as membrane fusion, protein trafficking, and bacterial cell wall biosynthesis.

Surfactants, also known as surface-active agents, are amphiphilic compounds that reduce the surface tension between two liquids or between a liquid and a solid. They contain both hydrophilic (water-soluble) and hydrophobic (water-insoluble) components in their molecular structure. This unique property allows them to interact with and stabilize interfaces, making them useful in various medical and healthcare applications.

In the medical field, surfactants are commonly used in pulmonary medicine, particularly for treating respiratory distress syndrome (RDS) in premature infants. The lungs of premature infants often lack sufficient amounts of natural lung surfactant, which can lead to RDS and other complications. Exogenous surfactants, derived from animal sources or synthetically produced, are administered to replace the missing or dysfunctional lung surfactant, improving lung compliance and gas exchange.

Surfactants also have applications in topical formulations for dermatology, as they can enhance drug penetration into the skin, reduce irritation, and improve the spreadability of creams and ointments. Additionally, they are used in diagnostic imaging to enhance contrast between tissues and improve visualization during procedures such as ultrasound and X-ray examinations.

A lung is a pair of spongy, elastic organs in the chest that work together to enable breathing. They are responsible for taking in oxygen and expelling carbon dioxide through the process of respiration. The left lung has two lobes, while the right lung has three lobes. The lungs are protected by the ribcage and are covered by a double-layered membrane called the pleura. The trachea divides into two bronchi, which further divide into smaller bronchioles, leading to millions of tiny air sacs called alveoli, where the exchange of gases occurs.

Pulmonary alveoli, also known as air sacs, are tiny clusters of air-filled pouches located at the end of the bronchioles in the lungs. They play a crucial role in the process of gas exchange during respiration. The thin walls of the alveoli, called alveolar membranes, allow oxygen from inhaled air to pass into the bloodstream and carbon dioxide from the bloodstream to pass into the alveoli to be exhaled out of the body. This vital function enables the lungs to supply oxygen-rich blood to the rest of the body and remove waste products like carbon dioxide.

Phospholipids are a major class of lipids that consist of a hydrophilic (water-attracting) head and two hydrophobic (water-repelling) tails. The head is composed of a phosphate group, which is often bound to an organic molecule such as choline, ethanolamine, serine or inositol. The tails are made up of two fatty acid chains.

Phospholipids are a key component of cell membranes and play a crucial role in maintaining the structural integrity and function of the cell. They form a lipid bilayer, with the hydrophilic heads facing outwards and the hydrophobic tails facing inwards, creating a barrier that separates the interior of the cell from the outside environment.

Phospholipids are also involved in various cellular processes such as signal transduction, intracellular trafficking, and protein function regulation. Additionally, they serve as emulsifiers in the digestive system, helping to break down fats in the diet.

In medical terms, 'air' is defined as the mixture of gases that make up the Earth's atmosphere. It primarily consists of nitrogen (78%), oxygen (21%), and small amounts of other gases such as argon, carbon dioxide, and trace amounts of neon, helium, and methane.

Air is essential for human life, as it provides the oxygen that our bodies need to produce energy through respiration. We inhale air into our lungs, where oxygen is absorbed into the bloodstream and transported to cells throughout the body. At the same time, carbon dioxide, a waste product of cellular metabolism, is exhaled out of the body through the lungs and back into the atmosphere.

In addition to its role in respiration, air also plays a critical role in regulating the Earth's climate and weather patterns, as well as serving as a medium for sound waves and other forms of energy transfer.

Adsorption is a process in which atoms, ions, or molecules from a gas, liquid, or dissolved solid accumulate on the surface of a material. This occurs because the particles in the adsorbate (the substance being adsorbed) have forces that attract them to the surface of the adsorbent (the material that the adsorbate is adhering to).

In medical terms, adsorption can refer to the use of materials with adsorptive properties to remove harmful substances from the body. For example, activated charcoal is sometimes used in the treatment of poisoning because it can adsorb a variety of toxic substances and prevent them from being absorbed into the bloodstream.

It's important to note that adsorption is different from absorption, which refers to the process by which a substance is taken up and distributed throughout a material or tissue.

Surface properties in the context of medical science refer to the characteristics and features of the outermost layer or surface of a biological material or structure, such as cells, tissues, organs, or medical devices. These properties can include physical attributes like roughness, smoothness, hydrophobicity or hydrophilicity, and electrical conductivity, as well as chemical properties like charge, reactivity, and composition.

In the field of biomaterials science, understanding surface properties is crucial for designing medical implants, devices, and drug delivery systems that can interact safely and effectively with biological tissues and fluids. Surface modifications, such as coatings or chemical treatments, can be used to alter surface properties and enhance biocompatibility, improve lubricity, reduce fouling, or promote specific cellular responses like adhesion, proliferation, or differentiation.

Similarly, in the field of cell biology, understanding surface properties is essential for studying cell-cell interactions, cell signaling, and cell behavior. Cells can sense and respond to changes in their environment, including variations in surface properties, which can influence cell shape, motility, and function. Therefore, characterizing and manipulating surface properties can provide valuable insights into the mechanisms of cellular processes and offer new strategies for developing therapies and treatments for various diseases.

Respiratory Distress Syndrome (RDS), Newborn is a common lung disorder in premature infants. It occurs when the lungs lack a substance called surfactant, which helps keep the tiny air sacs in the lungs open. This results in difficulty breathing and oxygenation, causing symptoms such as rapid, shallow breathing, grunting noises, flaring of the nostrils, and retractions (the skin between the ribs pulls in with each breath). RDS is more common in infants born before 34 weeks of gestation and is treated with surfactant replacement therapy, oxygen support, and mechanical ventilation if necessary. In severe cases, it can lead to complications such as bronchopulmonary dysplasia or even death.

Bronchoalveolar lavage (BAL) fluid is a type of clinical specimen obtained through a procedure called bronchoalveolar lavage. This procedure involves inserting a bronchoscope into the lungs and instilling a small amount of saline solution into a specific area of the lung, then gently aspirating the fluid back out. The fluid that is recovered is called bronchoalveolar lavage fluid.

BAL fluid contains cells and other substances that are present in the lower respiratory tract, including the alveoli (the tiny air sacs where gas exchange occurs). By analyzing BAL fluid, doctors can diagnose various lung conditions, such as pneumonia, interstitial lung disease, and lung cancer. They can also monitor the effectiveness of treatments for these conditions by comparing the composition of BAL fluid before and after treatment.

BAL fluid is typically analyzed for its cellular content, including the number and type of white blood cells present, as well as for the presence of bacteria, viruses, or other microorganisms. The fluid may also be tested for various proteins, enzymes, and other biomarkers that can provide additional information about lung health and disease.

According to the United States Food and Drug Administration (FDA), biological products are "products that are made from or contain a living organism or its derivatives, such as vaccines, blood and blood components, cells, genes, tissues, and proteins." These products can be composed of sugars, proteins, nucleic acids, or complex combinations of these substances, and they can come from many sources, including humans, animals, microorganisms, or plants.

Biological products are often used to diagnose, prevent, or treat a wide range of medical conditions, and they can be administered in various ways, such as through injection, inhalation, or topical application. Because biological products are derived from living organisms, their manufacturing processes can be complex and must be tightly controlled to ensure the safety, purity, and potency of the final product.

It's important to note that biological products are not the same as drugs, which are chemically synthesized compounds. While drugs are designed to interact with specific targets in the body, such as enzymes or receptors, biological products can have more complex and varied mechanisms of action, making them potentially more difficult to characterize and regulate.

Phosphatidylcholines (PtdCho) are a type of phospholipids that are essential components of cell membranes in living organisms. They are composed of a hydrophilic head group, which contains a choline moiety, and two hydrophobic fatty acid chains. Phosphatidylcholines are crucial for maintaining the structural integrity and function of cell membranes, and they also serve as important precursors for the synthesis of signaling molecules such as acetylcholine. They can be found in various tissues and biological fluids, including blood, and are abundant in foods such as soybeans, eggs, and meat. Phosphatidylcholines have been studied for their potential health benefits, including their role in maintaining healthy lipid metabolism and reducing the risk of cardiovascular disease.

Collectins are a group of proteins that belong to the collectin family, which are involved in the innate immune system. They are composed of a collagen-like region and a carbohydrate recognition domain (CRD), which allows them to bind to specific sugars on the surface of microorganisms, cells, and particles. Collectins play a crucial role in the defense against pathogens by promoting the clearance of microbes, modulating inflammation, and regulating immune responses.

Some examples of collectins include:

* Surfactant protein A (SP-A) and surfactant protein D (SP-D), which are found in the lungs and help to maintain the stability of the lung lining and protect against respiratory infections.
* Mannose-binding lectin (MBL), which is a serum protein that binds to mannose sugars on the surface of microorganisms, activating the complement system and promoting phagocytosis.
* Collectin liver 1 (CL-L1) and collectin kidney 1 (CL-K1), which are found in the liver and kidneys, respectively, and play a role in the clearance of apoptotic cells and immune complexes.

Deficiencies or mutations in collectins can lead to increased susceptibility to infections, autoimmune diseases, and other disorders.

Alveolar macrophages are a type of macrophage (a large phagocytic cell) that are found in the alveoli of the lungs. They play a crucial role in the immune defense system of the lungs by engulfing and destroying any foreign particles, such as dust, microorganisms, and pathogens, that enter the lungs through the process of inhalation. Alveolar macrophages also produce cytokines, which are signaling molecules that help to coordinate the immune response. They are important for maintaining the health and function of the lungs by removing debris and preventing infection.

Glycoproteins are complex proteins that contain oligosaccharide chains (glycans) covalently attached to their polypeptide backbone. These glycans are linked to the protein through asparagine residues (N-linked) or serine/threonine residues (O-linked). Glycoproteins play crucial roles in various biological processes, including cell recognition, cell-cell interactions, cell adhesion, and signal transduction. They are widely distributed in nature and can be found on the outer surface of cell membranes, in extracellular fluids, and as components of the extracellular matrix. The structure and composition of glycoproteins can vary significantly depending on their function and location within an organism.

Apoproteins are the protein components of lipoprotein complexes, which are responsible for transporting fat molecules, such as cholesterol and triglycerides, throughout the body. Apoproteins play a crucial role in the metabolism of lipids by acting as recognition signals that allow lipoproteins to interact with specific receptors on cell surfaces.

There are several different types of apoproteins, each with distinct functions. For example, apolipoprotein A-1 (apoA-1) is the major protein component of high-density lipoproteins (HDL), which are responsible for transporting excess cholesterol from tissues to the liver for excretion. Apolipoprotein B (apoB) is a large apoprotein found in low-density lipoproteins (LDL), very low-density lipoproteins (VLDL), and lipoprotein(a). ApoB plays a critical role in the assembly and secretion of VLDL from the liver, and it also mediates the uptake of LDL by cells.

Abnormalities in apoprotein levels or function can contribute to the development of various diseases, including cardiovascular disease, diabetes, and Alzheimer's disease. Therefore, measuring apoprotein levels in the blood can provide valuable information for diagnosing and monitoring these conditions.

Artificial membranes are synthetic or man-made materials that possess properties similar to natural biological membranes, such as selective permeability and barrier functions. These membranes can be designed to control the movement of molecules, ions, or cells across them, making them useful in various medical and biotechnological applications.

Examples of artificial membranes include:

1. Dialysis membranes: Used in hemodialysis for patients with renal failure, these semi-permeable membranes filter waste products and excess fluids from the blood while retaining essential proteins and cells.
2. Hemofiltration membranes: Utilized in extracorporeal circuits to remove larger molecules, such as cytokines or inflammatory mediators, from the blood during critical illnesses or sepsis.
3. Drug delivery systems: Artificial membranes can be used to encapsulate drugs, allowing for controlled release and targeted drug delivery in specific tissues or cells.
4. Tissue engineering: Synthetic membranes serve as scaffolds for cell growth and tissue regeneration, guiding the formation of new functional tissues.
5. Biosensors: Artificial membranes can be integrated into biosensing devices to selectively detect and quantify biomolecules, such as proteins or nucleic acids, in diagnostic applications.
6. Microfluidics: Artificial membranes are used in microfluidic systems for lab-on-a-chip applications, enabling the manipulation and analysis of small volumes of fluids for various medical and biological purposes.

Vernix caseosa is a medical term that refers to the white, cheesy, protective substance covering the skin of a newborn baby. It is composed of sebum (oil produced by the baby's sebaceous glands), dead skin cells, and water. This natural emollient provides a barrier against bacterial invasion and helps keep the baby's skin moisturized and supple. Vernix caseosa begins to form around the 20th week of gestation and is more abundant in premature infants than those born at term. It is typically washed off after birth, but some hospitals and midwives recommend leaving it on as long as possible due to its protective properties.

Immunoglobulin D (IgD) is a type of antibody that is present in the blood and other bodily fluids. It is one of the five classes of immunoglobulins (IgA, IgD, IgE, IgG, and IgM) found in humans and plays a role in the immune response.

IgD is produced by B cells, a type of white blood cell that is responsible for producing antibodies. It is primarily found on the surface of mature B cells, where it functions as a receptor for antigens (foreign substances that trigger an immune response). When an antigen binds to IgD on the surface of a B cell, it activates the B cell and stimulates it to produce and secrete antibodies specific to that antigen.

IgD is found in relatively low concentrations in the blood compared to other immunoglobulins, and its precise functions are not fully understood. However, it is thought to play a role in the regulation of B cell activation and the immune response. Additionally, some research suggests that IgD may have a direct role in protecting against certain types of infections.

It's worth noting that genetic deficiencies in IgD are not typically associated with any significant immunological abnormalities or increased susceptibility to infection.

Pulmonary Alveolar Proteinosis (PAP) is a rare lung disorder characterized by the accumulation of surfactant, a lipoprotein complex that reduces surface tension within the alveoli, in the air sacs (alveoli) of the lungs. This accumulation can lead to difficulty breathing and reduced oxygen levels in the blood.

There are three types of PAP:

1. Congenital PAP: A very rare inherited form that affects infants and is caused by a genetic mutation that disrupts the production or function of granulocyte-macrophage colony-stimulating factor (GM-CSF), a protein important for the development and function of alveolar macrophages.

2. Secondary PAP: This form is associated with conditions that impair the clearance of surfactant by alveolar macrophages, such as hematologic disorders (e.g., leukemia), infections, exposure to inhaled irritants (e.g., silica dust), and certain medications.

3. Idiopathic PAP: The most common form, also known as autoimmune PAP, is caused by the development of autoantibodies against GM-CSF, which disrupts its function and leads to surfactant accumulation in the lungs.

Treatment for PAP may include whole lung lavage (WLL), a procedure where the affected lung is filled with saline solution and then drained to remove excess surfactant, as well as managing any underlying conditions. In some cases of idiopathic PAP, off-label use of inhaled GM-CSF has shown promise in improving symptoms and lung function.

"Cattle" is a term used in the agricultural and veterinary fields to refer to domesticated animals of the genus *Bos*, primarily *Bos taurus* (European cattle) and *Bos indicus* (Zebu). These animals are often raised for meat, milk, leather, and labor. They are also known as bovines or cows (for females), bulls (intact males), and steers/bullocks (castrated males). However, in a strict medical definition, "cattle" does not apply to humans or other animals.

In medical terms, pressure is defined as the force applied per unit area on an object or body surface. It is often measured in millimeters of mercury (mmHg) in clinical settings. For example, blood pressure is the force exerted by circulating blood on the walls of the arteries and is recorded as two numbers: systolic pressure (when the heart beats and pushes blood out) and diastolic pressure (when the heart rests between beats).

Pressure can also refer to the pressure exerted on a wound or incision to help control bleeding, or the pressure inside the skull or spinal canal. High or low pressure in different body systems can indicate various medical conditions and require appropriate treatment.

Pneumocytes are specialized epithelial cells that line the alveoli, which are the tiny air sacs in the lungs where gas exchange occurs. There are two main types of pneumocytes: type I and type II.

Type I pneumocytes are flat, thin cells that cover about 95% of the alveolar surface area. They play a crucial role in facilitating the diffusion of oxygen and carbon dioxide between the alveoli and the bloodstream. Type I pneumocytes also contribute to maintaining the structural integrity of the alveoli.

Type II pneumocytes are smaller, more cuboidal cells that produce and secrete surfactant, a substance composed of proteins and lipids that reduces surface tension within the alveoli, preventing their collapse and facilitating breathing. Type II pneumocytes can also function as progenitor cells, capable of differentiating into type I pneumocytes to help repair damaged lung tissue.

In summary, pneumocytes are essential for maintaining proper gas exchange in the lungs and contributing to the overall health and functioning of the respiratory system.

Lung compliance is a measure of the ease with which the lungs expand and is defined as the change in lung volume for a given change in transpulmonary pressure. It is often expressed in units of liters per centimeter of water (L/cm H2O). A higher compliance indicates that the lungs are more easily distensible, while a lower compliance suggests that the lungs are stiffer and require more force to expand. Lung compliance can be affected by various conditions such as pulmonary fibrosis, pneumonia, acute respiratory distress syndrome (ARDS), and chronic obstructive pulmonary disease (COPD).

Meconium is the first stool passed by a newborn infant, typically within the first 48 hours of life. It is composed of materials ingested during fetal development, including intestinal epithelial cells, lanugo (fine hair), amniotic fluid, mucus, bile, and water. The color of meconium is usually greenish-black, and its consistency can range from a thick paste to a liquid. Meconium staining of the amniotic fluid can occur when the fetus has passed meconium while still in the uterus, which may indicate fetal distress and requires careful medical attention during delivery.

"Swine" is a common term used to refer to even-toed ungulates of the family Suidae, including domestic pigs and wild boars. However, in a medical context, "swine" often appears in the phrase "swine flu," which is a strain of influenza virus that typically infects pigs but can also cause illness in humans. The 2009 H1N1 pandemic was caused by a new strain of swine-origin influenza A virus, which was commonly referred to as "swine flu." It's important to note that this virus is not transmitted through eating cooked pork products; it spreads from person to person, mainly through respiratory droplets produced when an infected person coughs or sneezes.

4-Chloro-7-nitrobenzofurazan is not a medical term, but a chemical compound with the formula C6H2ClN3O4. It is an orange crystalline powder that is used in research and industrial applications, particularly as a reagent in chemical reactions. It is not a substance that is typically encountered in medical settings or treatments.

Medical definitions of water generally describe it as a colorless, odorless, tasteless liquid that is essential for all forms of life. It is a universal solvent, making it an excellent medium for transporting nutrients and waste products within the body. Water constitutes about 50-70% of an individual's body weight, depending on factors such as age, sex, and muscle mass.

In medical terms, water has several important functions in the human body:

1. Regulation of body temperature through perspiration and respiration.
2. Acting as a lubricant for joints and tissues.
3. Facilitating digestion by helping to break down food particles.
4. Transporting nutrients, oxygen, and waste products throughout the body.
5. Helping to maintain healthy skin and mucous membranes.
6. Assisting in the regulation of various bodily functions, such as blood pressure and heart rate.

Dehydration can occur when an individual does not consume enough water or loses too much fluid due to illness, exercise, or other factors. This can lead to a variety of symptoms, including dry mouth, fatigue, dizziness, and confusion. Severe dehydration can be life-threatening if left untreated.

Lung diseases refer to a broad category of disorders that affect the lungs and other structures within the respiratory system. These diseases can impair lung function, leading to symptoms such as coughing, shortness of breath, chest pain, and wheezing. They can be categorized into several types based on the underlying cause and nature of the disease process. Some common examples include:

1. Obstructive lung diseases: These are characterized by narrowing or blockage of the airways, making it difficult to breathe out. Examples include chronic obstructive pulmonary disease (COPD), asthma, bronchiectasis, and cystic fibrosis.
2. Restrictive lung diseases: These involve stiffening or scarring of the lungs, which reduces their ability to expand and take in air. Examples include idiopathic pulmonary fibrosis, sarcoidosis, and asbestosis.
3. Infectious lung diseases: These are caused by bacteria, viruses, fungi, or parasites that infect the lungs. Examples include pneumonia, tuberculosis, and influenza.
4. Vascular lung diseases: These affect the blood vessels in the lungs, impairing oxygen exchange. Examples include pulmonary embolism, pulmonary hypertension, and chronic thromboembolic pulmonary hypertension (CTEPH).
5. Neoplastic lung diseases: These involve abnormal growth of cells within the lungs, leading to cancer. Examples include small cell lung cancer, non-small cell lung cancer, and mesothelioma.
6. Other lung diseases: These include interstitial lung diseases, pleural effusions, and rare disorders such as pulmonary alveolar proteinosis and lymphangioleiomyomatosis (LAM).

It is important to note that this list is not exhaustive, and there are many other conditions that can affect the lungs. Proper diagnosis and treatment of lung diseases require consultation with a healthcare professional, such as a pulmonologist or respiratory therapist.

Molecular sequence data refers to the specific arrangement of molecules, most commonly nucleotides in DNA or RNA, or amino acids in proteins, that make up a biological macromolecule. This data is generated through laboratory techniques such as sequencing, and provides information about the exact order of the constituent molecules. This data is crucial in various fields of biology, including genetics, evolution, and molecular biology, allowing for comparisons between different organisms, identification of genetic variations, and studies of gene function and regulation.

Serum globulins are a group of proteins present in the liquid portion of blood, known as serum. They are produced by the immune system in response to foreign substances such as bacteria, viruses, and allergens. Serum globulins include several types of immunoglobulins (antibodies), complement components, and other proteins involved in the immune response.

The serum globulin level is often measured as part of a complete blood count (CBC) or a protein electrophoresis test. An elevated serum globulin level may indicate an ongoing infection, inflammation, or an autoimmune disorder. Conversely, a decreased level may suggest a liver or kidney disease, or a malnutrition condition. It is important to note that the interpretation of serum globulin levels should be done in conjunction with other laboratory and clinical findings.

Amniotic fluid is a clear, slightly yellowish liquid that surrounds and protects the developing baby in the uterus. It is enclosed within the amniotic sac, which is a thin-walled sac that forms around the embryo during early pregnancy. The fluid is composed of fetal urine, lung secretions, and fluids that cross over from the mother's bloodstream through the placenta.

Amniotic fluid plays several important roles in pregnancy:

1. It provides a shock-absorbing cushion for the developing baby, protecting it from injury caused by movement or external forces.
2. It helps to maintain a constant temperature around the fetus, keeping it warm and comfortable.
3. It allows the developing baby to move freely within the uterus, promoting normal growth and development of the muscles and bones.
4. It provides a source of nutrients and hydration for the fetus, helping to support its growth and development.
5. It helps to prevent infection by providing a barrier between the fetus and the outside world.

Throughout pregnancy, the volume of amniotic fluid increases as the fetus grows. The amount of fluid typically peaks around 34-36 weeks of gestation, after which it begins to gradually decrease. Abnormalities in the volume of amniotic fluid can indicate problems with the developing baby or the pregnancy itself, and may require medical intervention.

A lipid bilayer is a thin membrane made up of two layers of lipid molecules, primarily phospholipids. The hydrophilic (water-loving) heads of the lipids face outwards, coming into contact with watery environments on both sides, while the hydrophobic (water-fearing) tails point inward, away from the aqueous surroundings. This unique structure allows lipid bilayers to form a stable barrier that controls the movement of molecules and ions in and out of cells and organelles, thus playing a crucial role in maintaining cellular compartmentalization and homeostasis.

An amino acid sequence is the specific order of amino acids in a protein or peptide molecule, formed by the linking of the amino group (-NH2) of one amino acid to the carboxyl group (-COOH) of another amino acid through a peptide bond. The sequence is determined by the genetic code and is unique to each type of protein or peptide. It plays a crucial role in determining the three-dimensional structure and function of proteins.

"Laureates" is not a medical term. However, if you are referring to "laurates" as a salt or ester of lauric acid, then here's the definition:

Laurates are organic compounds that contain a laurate group, which is the anion (negatively charged ion) derived from lauric acid. Lauric acid is a saturated fatty acid with a 12-carbon chain, and its anion has the chemical formula CH3(CH2)10COO-.

Laurates can be formed by reacting lauric acid with a base to form a salt (e.g., sodium laurate, potassium laurate) or by reacting it with an alcohol to form an ester (e.g., methyl laurate, ethyl laurate). These compounds have various applications in industry, including as surfactants, emulsifiers, and solubilizers in personal care products, cosmetics, and pharmaceuticals.

Respiratory Distress Syndrome, Adult (RDSa or ARDS), also known as Acute Respiratory Distress Syndrome, is a severe form of acute lung injury characterized by rapid onset of widespread inflammation in the lungs. This results in increased permeability of the alveolar-capillary membrane, pulmonary edema, and hypoxemia (low oxygen levels in the blood). The inflammation can be triggered by various direct or indirect insults to the lung, such as sepsis, pneumonia, trauma, or aspiration.

The hallmark of ARDS is the development of bilateral pulmonary infiltrates on chest X-ray, which can resemble pulmonary edema, but without evidence of increased left atrial pressure. The condition can progress rapidly and may require mechanical ventilation with positive end-expiratory pressure (PEEP) to maintain adequate oxygenation and prevent further lung injury.

The management of ARDS is primarily supportive, focusing on protecting the lungs from further injury, optimizing oxygenation, and providing adequate nutrition and treatment for any underlying conditions. The use of low tidal volumes and limiting plateau pressures during mechanical ventilation have been shown to improve outcomes in patients with ARDS.

Lipids are a broad group of organic compounds that are insoluble in water but soluble in nonpolar organic solvents. They include fats, waxes, sterols, fat-soluble vitamins (such as vitamins A, D, E, and K), monoglycerides, diglycerides, triglycerides, and phospholipids. Lipids serve many important functions in the body, including energy storage, acting as structural components of cell membranes, and serving as signaling molecules. High levels of certain lipids, particularly cholesterol and triglycerides, in the blood are associated with an increased risk of cardiovascular disease.

"Fetal organ maturity" refers to the stage of development and functional competency of the various organs in a fetus. It is the point at which an organ has developed enough to be able to perform its intended physiological functions effectively and sustainably. This maturity is determined by a combination of factors including structural development, cellular differentiation, and biochemical functionality.

Fetal organ maturity is a critical aspect of fetal development, as it directly impacts the newborn's ability to survive and thrive outside the womb. The level of maturity varies among different organs, with some becoming mature earlier in gestation while others continue to develop and mature until birth or even after.

Assessment of fetal organ maturity is often used in clinical settings to determine the optimal time for delivery, particularly in cases where there are risks associated with premature birth. This assessment typically involves a combination of imaging studies, such as ultrasound and MRI, as well as laboratory tests and physical examinations.

Hyaline Membrane Disease (HMD) is a medical condition primarily seen in newborns, also known as Infant Respiratory Distress Syndrome (IRDS). It's characterized by the presence of hyaline membranes, which are made up of proteins and cellular debris, on the inside surfaces of the alveoli (air sacs) in the lungs.

These membranes can interfere with the normal gas exchange process, making it difficult for the newborn to breathe effectively. The condition is often associated with premature birth, as the surfactant that coats the inside of the lungs and keeps them inflated isn't fully produced until around the 35th week of gestation.

The lack of sufficient surfactant can lead to collapse of the alveoli (atelectasis), inflammation, and the formation of hyaline membranes. HMD is a significant cause of morbidity and mortality in premature infants, but with early detection and proper medical care, including the use of artificial surfactant, oxygen therapy, and mechanical ventilation, many babies can recover.

Atomic Force Microscopy (AFM) is a type of microscopy that allows visualization and measurement of surfaces at the atomic level. It works by using a sharp probe, called a tip, that is mounted on a flexible cantilever. The tip is brought very close to the surface of the sample and as the sample is scanned, the forces between the tip and the sample cause the cantilever to deflect. This deflection is measured and used to generate a topographic map of the surface with extremely high resolution, often on the order of fractions of a nanometer. AFM can be used to study both conductive and non-conductive samples, and can operate in various environments, including air and liquid. It has applications in fields such as materials science, biology, and chemistry.

Respiratory aspiration is defined as the entry of foreign materials (such as food, liquids, or vomit) into the lower respiratory tract during swallowing, which includes the trachea and lungs. This can lead to respiratory complications such as pneumonia, bronchitis, or lung abscesses. Aspiration can occur in individuals with impaired swallowing function due to various conditions like neurological disorders, stroke, or anesthesia.

A fetus is the developing offspring in a mammal, from the end of the embryonic period (approximately 8 weeks after fertilization in humans) until birth. In humans, the fetal stage of development starts from the eleventh week of pregnancy and continues until childbirth, which is termed as full-term pregnancy at around 37 to 40 weeks of gestation. During this time, the organ systems become fully developed and the body grows in size. The fetus is surrounded by the amniotic fluid within the amniotic sac and is connected to the placenta via the umbilical cord, through which it receives nutrients and oxygen from the mother. Regular prenatal care is essential during this period to monitor the growth and development of the fetus and ensure a healthy pregnancy and delivery.

I believe there may be some confusion in your question. "Rabbits" is a common name used to refer to the Lagomorpha species, particularly members of the family Leporidae. They are small mammals known for their long ears, strong legs, and quick reproduction.

However, if you're referring to "rabbits" in a medical context, there is a term called "rabbit syndrome," which is a rare movement disorder characterized by repetitive, involuntary movements of the fingers, resembling those of a rabbit chewing. It is also known as "finger-chewing chorea." This condition is usually associated with certain medications, particularly antipsychotics, and typically resolves when the medication is stopped or adjusted.

Bronchoalveolar lavage (BAL) is a medical procedure in which a small amount of fluid is introduced into a segment of the lung and then gently suctioned back out. The fluid contains cells and other materials that can be analyzed to help diagnose various lung conditions, such as inflammation, infection, or cancer.

The procedure is typically performed during bronchoscopy, which involves inserting a thin, flexible tube with a light and camera on the end through the nose or mouth and into the lungs. Once the bronchoscope is in place, a small catheter is passed through the bronchoscope and into the desired lung segment. The fluid is then introduced and suctioned back out, and the sample is sent to a laboratory for analysis.

BAL can be helpful in diagnosing various conditions such as pneumonia, interstitial lung diseases, alveolar proteinosis, and some types of cancer. It can also be used to monitor the effectiveness of treatment for certain lung conditions. However, like any medical procedure, it carries some risks, including bleeding, infection, and respiratory distress. Therefore, it is important that the procedure is performed by a qualified healthcare professional in a controlled setting.

I'm sorry for any confusion, but "quartz" is not a medical term. Quartz is a mineral that is one of the most common minerals on Earth. It is found in many different types of rocks and is made up of silicon dioxide (SiO2). It is often used in electronics and watches because of its piezoelectric properties, which means it can generate an electric charge when subjected to pressure or stress.

It does not have any direct relation with medical field, although there are some Quartz based equipment like quartz crystal microbalance (QCM) sensors that are used in medical research for the detection of biomolecules and pathogens.

A phase transition in the context of medicine and physiology often refers to the transformation of a substance or matter from one state to another within the body, typically in relation to temperature or pressure changes. However, I couldn't find a widely accepted medical definition for "phase transition."

In physics and chemistry, a phase transition is a process where a thermodynamic system changes from one phase or state of matter to another, such as:

1. Solid to liquid (melting)
2. Liquid to gas (vaporization)
3. Gas to liquid (condensation)
4. Solid to gas (sublimation)
5. Changes between different crystalline structures of the same substance (polymorphic phase transitions)

While not a direct medical definition, these concepts are relevant in various biochemical and physiological processes, such as protein folding, cell membrane fluidity, and temperature regulation in the body.

Biophysical phenomena refer to the observable events and processes that occur in living organisms, which can be explained and studied using the principles and methods of physics. These phenomena can include a wide range of biological processes at various levels of organization, from molecular interactions to whole-organism behaviors. Examples of biophysical phenomena include the mechanics of muscle contraction, the electrical activity of neurons, the transport of molecules across cell membranes, and the optical properties of biological tissues. By applying physical theories and techniques to the study of living systems, biophysicists seek to better understand the fundamental principles that govern life and to develop new approaches for diagnosing and treating diseases.

2-Naphthylamine is a crystalline solid organic compound that is classified as a primary aromatic amine. Its chemical formula is C10H9N. It is an intensely orange-red to reddish-brown substance that is slightly soluble in water and more soluble in organic solvents.

2-Naphthylamine is produced by the reduction of 2-naphthol or its derivatives. Historically, it was used as an intermediate in the synthesis of azo dyes and other chemical compounds. However, due to its toxicity and carcinogenicity, its use has been largely discontinued in many industries.

Exposure to 2-Naphthylamine can occur through inhalation, skin contact, or ingestion, and it has been associated with an increased risk of bladder cancer and other health effects. Therefore, appropriate safety measures must be taken when handling this compound, including the use of personal protective equipment (PPE) such as gloves, lab coats, and eye protection.

Recombinant proteins are artificially created proteins produced through the use of recombinant DNA technology. This process involves combining DNA molecules from different sources to create a new set of genes that encode for a specific protein. The resulting recombinant protein can then be expressed, purified, and used for various applications in research, medicine, and industry.

Recombinant proteins are widely used in biomedical research to study protein function, structure, and interactions. They are also used in the development of diagnostic tests, vaccines, and therapeutic drugs. For example, recombinant insulin is a common treatment for diabetes, while recombinant human growth hormone is used to treat growth disorders.

The production of recombinant proteins typically involves the use of host cells, such as bacteria, yeast, or mammalian cells, which are engineered to express the desired protein. The host cells are transformed with a plasmid vector containing the gene of interest, along with regulatory elements that control its expression. Once the host cells are cultured and the protein is expressed, it can be purified using various chromatography techniques.

Overall, recombinant proteins have revolutionized many areas of biology and medicine, enabling researchers to study and manipulate proteins in ways that were previously impossible.

Biophysics is a interdisciplinary field that combines the principles and methods of physics with those of biology to study biological systems and phenomena. It involves the use of physical theories, models, and techniques to understand and explain the properties, functions, and behaviors of living organisms and their constituents, such as cells, proteins, and DNA.

Biophysics can be applied to various areas of biology, including molecular biology, cell biology, neuroscience, and physiology. It can help elucidate the mechanisms of biological processes at the molecular and cellular levels, such as protein folding, ion transport, enzyme kinetics, gene expression, and signal transduction. Biophysical methods can also be used to develop diagnostic and therapeutic tools for medical applications, such as medical imaging, drug delivery, and gene therapy.

Examples of biophysical techniques include X-ray crystallography, nuclear magnetic resonance (NMR) spectroscopy, electron microscopy, fluorescence microscopy, atomic force microscopy, and computational modeling. These methods allow researchers to probe the structure, dynamics, and interactions of biological molecules and systems with high precision and resolution, providing insights into their functions and behaviors.

Protein binding, in the context of medical and biological sciences, refers to the interaction between a protein and another molecule (known as the ligand) that results in a stable complex. This process is often reversible and can be influenced by various factors such as pH, temperature, and concentration of the involved molecules.

In clinical chemistry, protein binding is particularly important when it comes to drugs, as many of them bind to proteins (especially albumin) in the bloodstream. The degree of protein binding can affect a drug's distribution, metabolism, and excretion, which in turn influence its therapeutic effectiveness and potential side effects.

Protein-bound drugs may be less available for interaction with their target tissues, as only the unbound or "free" fraction of the drug is active. Therefore, understanding protein binding can help optimize dosing regimens and minimize adverse reactions.

Temperature, in a medical context, is a measure of the degree of hotness or coldness of a body or environment. It is usually measured using a thermometer and reported in degrees Celsius (°C), degrees Fahrenheit (°F), or kelvin (K). In the human body, normal core temperature ranges from about 36.5-37.5°C (97.7-99.5°F) when measured rectally, and can vary slightly depending on factors such as time of day, physical activity, and menstrual cycle. Elevated body temperature is a common sign of infection or inflammation, while abnormally low body temperature can indicate hypothermia or other medical conditions.

Agglutination is a medical term that refers to the clumping together of particles, such as cells, bacteria, or precipitates, in a liquid medium. It most commonly occurs due to the presence of antibodies in the fluid that bind to specific antigens on the surface of the particles, causing them to adhere to one another and form visible clumps.

In clinical laboratory testing, agglutination is often used as a diagnostic tool to identify the presence of certain antibodies or antigens in a patient's sample. For example, a common application of agglutination is in blood typing, where the presence of specific antigens on the surface of red blood cells causes them to clump together when mixed with corresponding antibodies.

Agglutination can also occur in response to certain infectious agents, such as bacteria or viruses, that display antigens on their surface. In these cases, the agglutination reaction can help diagnose an infection and guide appropriate treatment.

Carbon nanotubes (CNTs) are defined in medical literature as hollow, cylindrical structures composed of rolled graphene sheets, with diameters typically measuring on the nanoscale (ranging from 1 to several tens of nanometers) and lengths that can reach several micrometers. They can be single-walled (SWCNTs), consisting of a single layer of graphene, or multi-walled (MWCNTs), composed of multiple concentric layers of graphene.

Carbon nanotubes have unique mechanical, electrical, and thermal properties that make them promising for various biomedical applications, such as drug delivery systems, biosensors, and tissue engineering scaffolds. However, their potential toxicity and long-term effects on human health are still under investigation, particularly concerning their ability to induce oxidative stress, inflammation, and genotoxicity in certain experimental settings.

A newborn infant is a baby who is within the first 28 days of life. This period is also referred to as the neonatal period. Newborns require specialized care and attention due to their immature bodily systems and increased vulnerability to various health issues. They are closely monitored for signs of well-being, growth, and development during this critical time.

Cetrimonium compounds are a type of chemical compound that contain cetrimonium as the active ingredient. Cetrimonium is a quaternary ammonium compound that has antimicrobial and surfactant properties. It is commonly used in personal care products such as shampoos, conditioners, and cosmetics as a preservative and to improve the product's ability to spread and wet surfaces.

Cetrimonium compounds are often used as a alternative to formaldehyde-releasing preservatives, which have been linked to health concerns. They work by disrupting the bacterial cell membrane, leading to cell death. Cetrimonium compounds are also effective against fungi and viruses.

In addition to their use in personal care products, cetrimonium compounds are also used in medical settings as a antiseptic and disinfectant. They are often found in products used to clean and disinfect medical equipment and surfaces.

It is important to note that while cetrimonium compounds have been deemed safe for use in personal care products and medical settings, they can cause irritation and allergic reactions in some people. It is always recommended to do a patch test before using a new product containing cetrimonium compounds.

Sprague-Dawley rats are a strain of albino laboratory rats that are widely used in scientific research. They were first developed by researchers H.H. Sprague and R.C. Dawley in the early 20th century, and have since become one of the most commonly used rat strains in biomedical research due to their relatively large size, ease of handling, and consistent genetic background.

Sprague-Dawley rats are outbred, which means that they are genetically diverse and do not suffer from the same limitations as inbred strains, which can have reduced fertility and increased susceptibility to certain diseases. They are also characterized by their docile nature and low levels of aggression, making them easier to handle and study than some other rat strains.

These rats are used in a wide variety of research areas, including toxicology, pharmacology, nutrition, cancer, and behavioral studies. Because they are genetically diverse, Sprague-Dawley rats can be used to model a range of human diseases and conditions, making them an important tool in the development of new drugs and therapies.

Liposomes are artificially prepared, small, spherical vesicles composed of one or more lipid bilayers that enclose an aqueous compartment. They can encapsulate both hydrophilic and hydrophobic drugs, making them useful for drug delivery applications in the medical field. The lipid bilayer structure of liposomes is similar to that of biological membranes, which allows them to merge with and deliver their contents into cells. This property makes liposomes a valuable tool in delivering drugs directly to targeted sites within the body, improving drug efficacy while minimizing side effects.

Differential scanning calorimetry (DSC) is a thermoanalytical technique used to measure the difference in the amount of heat required to increase the temperature of a sample and a reference as a function of temperature. It is commonly used to study phase transitions, such as melting, crystallization, and glass transition, as well as chemical reactions, in a wide range of materials, including polymers, pharmaceuticals, and biological samples.

In DSC, the sample and reference are placed in separate pans and heated at a constant rate. The heat flow required to maintain this heating rate is continuously measured for both the sample and the reference. As the temperature of the sample changes during a phase transition or chemical reaction, the heat flow required to maintain the same heating rate will change relative to the reference. This allows for the measurement of the enthalpy change (ΔH) associated with the transition or reaction.

Differential scanning calorimetry is a powerful tool in materials science and research as it can provide information about the thermal behavior, stability, and composition of materials. It can also be used to study the kinetics of reactions and phase transitions, making it useful for optimizing processing conditions and developing new materials.

"Phleum" is the genus name for a group of plants commonly known as Timothy-grass or Cat's-tail. It is a type of grass that is widely used in agriculture and gardening. I believe you might be looking for a medical term related to "phleum," so let me clarify:

In medical terminology, the term "phleum" is not commonly used. However, if you are referring to "phlebothrombosis," it is a term that could be relevant. Phlebothrombosis refers to the formation of a blood clot (thrombus) within a vein, which can occur due to various medical conditions or situations, such as immobility, surgery, or certain diseases. The term "phlebo-" means vein, and "-thrombosis" refers to the formation of a thrombus or blood clot.

If this is not the term you were looking for, please provide more context or clarify your question so I can give you a more accurate answer.

Silicon dioxide is not a medical term, but a chemical compound with the formula SiO2. It's commonly known as quartz or sand and is not something that would typically have a medical definition. However, in some cases, silicon dioxide can be used in pharmaceutical preparations as an excipient (an inactive substance that serves as a vehicle or medium for a drug) or as a food additive, often as an anti-caking agent.

In these contexts, it's important to note that silicon dioxide is considered generally recognized as safe (GRAS) by the U.S. Food and Drug Administration (FDA). However, exposure to very high levels of respirable silica dust, such as in certain industrial settings, can increase the risk of lung disease, including silicosis.

"Cells, cultured" is a medical term that refers to cells that have been removed from an organism and grown in controlled laboratory conditions outside of the body. This process is called cell culture and it allows scientists to study cells in a more controlled and accessible environment than they would have inside the body. Cultured cells can be derived from a variety of sources, including tissues, organs, or fluids from humans, animals, or cell lines that have been previously established in the laboratory.

Cell culture involves several steps, including isolation of the cells from the tissue, purification and characterization of the cells, and maintenance of the cells in appropriate growth conditions. The cells are typically grown in specialized media that contain nutrients, growth factors, and other components necessary for their survival and proliferation. Cultured cells can be used for a variety of purposes, including basic research, drug development and testing, and production of biological products such as vaccines and gene therapies.

It is important to note that cultured cells may behave differently than they do in the body, and results obtained from cell culture studies may not always translate directly to human physiology or disease. Therefore, it is essential to validate findings from cell culture experiments using additional models and ultimately in clinical trials involving human subjects.

Porphobilinogen (PBG) is a bioactive compound that plays a crucial role in the biosynthesis pathway of heme, which is an essential component of hemoglobin and other hemoproteins. It is a porphyrin precursor and is synthesized from aminolevulinic acid (ALA) by the enzyme ALA dehydratase in the second step of heme biosynthesis.

In medical terms, abnormal accumulation or increased levels of PBG in the body can indicate an underlying disorder in heme biosynthesis, such as acute intermittent porphyria (AIP), variegate porphyria (VP), or hereditary coproporphyria (HCP). These disorders are known as porphyrias and are characterized by the buildup of porphyrin precursors in various tissues, leading to neurological and gastrointestinal symptoms.

Therefore, measuring PBG levels in urine or blood can help diagnose and monitor these conditions.

Messenger RNA (mRNA) is a type of RNA (ribonucleic acid) that carries genetic information copied from DNA in the form of a series of three-base code "words," each of which specifies a particular amino acid. This information is used by the cell's machinery to construct proteins, a process known as translation. After being transcribed from DNA, mRNA travels out of the nucleus to the ribosomes in the cytoplasm where protein synthesis occurs. Once the protein has been synthesized, the mRNA may be degraded and recycled. Post-transcriptional modifications can also occur to mRNA, such as alternative splicing and addition of a 5' cap and a poly(A) tail, which can affect its stability, localization, and translation efficiency.

Electron microscopy (EM) is a type of microscopy that uses a beam of electrons to create an image of the sample being examined, resulting in much higher magnification and resolution than light microscopy. There are several types of electron microscopy, including transmission electron microscopy (TEM), scanning electron microscopy (SEM), and reflection electron microscopy (REM).

In TEM, a beam of electrons is transmitted through a thin slice of the sample, and the electrons that pass through the sample are focused to form an image. This technique can provide detailed information about the internal structure of cells, viruses, and other biological specimens, as well as the composition and structure of materials at the atomic level.

In SEM, a beam of electrons is scanned across the surface of the sample, and the electrons that are scattered back from the surface are detected to create an image. This technique can provide information about the topography and composition of surfaces, as well as the structure of materials at the microscopic level.

REM is a variation of SEM in which the beam of electrons is reflected off the surface of the sample, rather than scattered back from it. This technique can provide information about the surface chemistry and composition of materials.

Electron microscopy has a wide range of applications in biology, medicine, and materials science, including the study of cellular structure and function, disease diagnosis, and the development of new materials and technologies.

Palmitic acid is a type of saturated fatty acid, which is a common component in many foods and also produced naturally by the human body. Its chemical formula is C16H32O2. It's named after palm trees because it was first isolated from palm oil, although it can also be found in other vegetable oils, animal fats, and dairy products.

In the human body, palmitic acid plays a role in energy production and storage. However, consuming large amounts of this fatty acid has been linked to an increased risk of heart disease due to its association with elevated levels of bad cholesterol (LDL). The World Health Organization recommends limiting the consumption of saturated fats, including palmitic acid, to less than 10% of total energy intake.

Micelles are structures formed in a solution when certain substances, such as surfactants, reach a critical concentration called the critical micelle concentration (CMC). At this concentration, these molecules, which have both hydrophilic (water-attracting) and hydrophobic (water-repelling) components, arrange themselves in a spherical shape with the hydrophilic parts facing outward and the hydrophobic parts clustered inside. This formation allows the hydrophobic components to avoid contact with water while the hydrophilic components interact with it. Micelles are important in various biological and industrial processes, such as drug delivery, soil remediation, and the formation of emulsions.

Phagocytosis is the process by which certain cells in the body, known as phagocytes, engulf and destroy foreign particles, bacteria, or dead cells. This mechanism plays a crucial role in the immune system's response to infection and inflammation. Phagocytes, such as neutrophils, monocytes, and macrophages, have receptors on their surface that recognize and bind to specific molecules (known as antigens) on the target particles or microorganisms.

Once attached, the phagocyte extends pseudopodia (cell extensions) around the particle, forming a vesicle called a phagosome that completely encloses it. The phagosome then fuses with a lysosome, an intracellular organelle containing digestive enzymes and other chemicals. This fusion results in the formation of a phagolysosome, where the engulfed particle is broken down by the action of these enzymes, neutralizing its harmful effects and allowing for the removal of cellular debris or pathogens.

Phagocytosis not only serves as a crucial defense mechanism against infections but also contributes to tissue homeostasis by removing dead cells and debris.

Respiratory mucosa refers to the mucous membrane that lines the respiratory tract, including the nose, throat, bronchi, and lungs. It is a specialized type of tissue that is composed of epithelial cells, goblet cells, and glands that produce mucus, which helps to trap inhaled particles such as dust, allergens, and pathogens.

The respiratory mucosa also contains cilia, tiny hair-like structures that move rhythmically to help propel the mucus and trapped particles out of the airways and into the upper part of the throat, where they can be swallowed or coughed up. This defense mechanism is known as the mucociliary clearance system.

In addition to its role in protecting the respiratory tract from harmful substances, the respiratory mucosa also plays a crucial role in immune function by containing various types of immune cells that help to detect and respond to pathogens and other threats.

I apologize, but "sheep" is not a term that has a medical definition. It is a common animal with the scientific name Ovis aries. If you have any medical or health-related questions, I would be happy to try and help answer those for you.

Electrophoresis, polyacrylamide gel (EPG) is a laboratory technique used to separate and analyze complex mixtures of proteins or nucleic acids (DNA or RNA) based on their size and electrical charge. This technique utilizes a matrix made of cross-linked polyacrylamide, a type of gel, which provides a stable and uniform environment for the separation of molecules.

In this process:

1. The polyacrylamide gel is prepared by mixing acrylamide monomers with a cross-linking agent (bis-acrylamide) and a catalyst (ammonium persulfate) in the presence of a buffer solution.
2. The gel is then poured into a mold and allowed to polymerize, forming a solid matrix with uniform pore sizes that depend on the concentration of acrylamide used. Higher concentrations result in smaller pores, providing better resolution for separating smaller molecules.
3. Once the gel has set, it is placed in an electrophoresis apparatus containing a buffer solution. Samples containing the mixture of proteins or nucleic acids are loaded into wells on the top of the gel.
4. An electric field is applied across the gel, causing the negatively charged molecules to migrate towards the positive electrode (anode) while positively charged molecules move toward the negative electrode (cathode). The rate of migration depends on the size, charge, and shape of the molecules.
5. Smaller molecules move faster through the gel matrix and will migrate farther from the origin compared to larger molecules, resulting in separation based on size. Proteins and nucleic acids can be selectively stained after electrophoresis to visualize the separated bands.

EPG is widely used in various research fields, including molecular biology, genetics, proteomics, and forensic science, for applications such as protein characterization, DNA fragment analysis, cloning, mutation detection, and quality control of nucleic acid or protein samples.

In the field of medicine, "time factors" refer to the duration of symptoms or time elapsed since the onset of a medical condition, which can have significant implications for diagnosis and treatment. Understanding time factors is crucial in determining the progression of a disease, evaluating the effectiveness of treatments, and making critical decisions regarding patient care.

For example, in stroke management, "time is brain," meaning that rapid intervention within a specific time frame (usually within 4.5 hours) is essential to administering tissue plasminogen activator (tPA), a clot-busting drug that can minimize brain damage and improve patient outcomes. Similarly, in trauma care, the "golden hour" concept emphasizes the importance of providing definitive care within the first 60 minutes after injury to increase survival rates and reduce morbidity.

Time factors also play a role in monitoring the progression of chronic conditions like diabetes or heart disease, where regular follow-ups and assessments help determine appropriate treatment adjustments and prevent complications. In infectious diseases, time factors are crucial for initiating antibiotic therapy and identifying potential outbreaks to control their spread.

Overall, "time factors" encompass the significance of recognizing and acting promptly in various medical scenarios to optimize patient outcomes and provide effective care.

In the context of medicine and pharmacology, "kinetics" refers to the study of how a drug moves throughout the body, including its absorption, distribution, metabolism, and excretion (often abbreviated as ADME). This field is called "pharmacokinetics."

1. Absorption: This is the process of a drug moving from its site of administration into the bloodstream. Factors such as the route of administration (e.g., oral, intravenous, etc.), formulation, and individual physiological differences can affect absorption.

2. Distribution: Once a drug is in the bloodstream, it gets distributed throughout the body to various tissues and organs. This process is influenced by factors like blood flow, protein binding, and lipid solubility of the drug.

3. Metabolism: Drugs are often chemically modified in the body, typically in the liver, through processes known as metabolism. These changes can lead to the formation of active or inactive metabolites, which may then be further distributed, excreted, or undergo additional metabolic transformations.

4. Excretion: This is the process by which drugs and their metabolites are eliminated from the body, primarily through the kidneys (urine) and the liver (bile).

Understanding the kinetics of a drug is crucial for determining its optimal dosing regimen, potential interactions with other medications or foods, and any necessary adjustments for special populations like pediatric or geriatric patients, or those with impaired renal or hepatic function.

Lectins are a type of proteins that bind specifically to carbohydrates and have been found in various plant and animal sources. They play important roles in biological recognition events, such as cell-cell adhesion, and can also be involved in the immune response. Some lectins can agglutinate certain types of cells or precipitate glycoproteins, while others may have a more direct effect on cellular processes. In some cases, lectins from plants can cause adverse effects in humans if ingested, such as digestive discomfort or allergic reactions.

A base sequence in the context of molecular biology refers to the specific order of nucleotides in a DNA or RNA molecule. In DNA, these nucleotides are adenine (A), guanine (G), cytosine (C), and thymine (T). In RNA, uracil (U) takes the place of thymine. The base sequence contains genetic information that is transcribed into RNA and ultimately translated into proteins. It is the exact order of these bases that determines the genetic code and thus the function of the DNA or RNA molecule.

Fluorescence microscopy is a type of microscopy that uses fluorescent dyes or proteins to highlight and visualize specific components within a sample. In this technique, the sample is illuminated with high-energy light, typically ultraviolet (UV) or blue light, which excites the fluorescent molecules causing them to emit lower-energy, longer-wavelength light, usually visible light in the form of various colors. This emitted light is then collected by the microscope and detected to produce an image.

Fluorescence microscopy has several advantages over traditional brightfield microscopy, including the ability to visualize specific structures or molecules within a complex sample, increased sensitivity, and the potential for quantitative analysis. It is widely used in various fields of biology and medicine, such as cell biology, neuroscience, and pathology, to study the structure, function, and interactions of cells and proteins.

There are several types of fluorescence microscopy techniques, including widefield fluorescence microscopy, confocal microscopy, two-photon microscopy, and total internal reflection fluorescence (TIRF) microscopy, each with its own strengths and limitations. These techniques can provide valuable insights into the behavior of cells and proteins in health and disease.

Peptides are short chains of amino acid residues linked by covalent bonds, known as peptide bonds. They are formed when two or more amino acids are joined together through a condensation reaction, which results in the elimination of a water molecule and the formation of an amide bond between the carboxyl group of one amino acid and the amino group of another.

Peptides can vary in length from two to about fifty amino acids, and they are often classified based on their size. For example, dipeptides contain two amino acids, tripeptides contain three, and so on. Oligopeptides typically contain up to ten amino acids, while polypeptides can contain dozens or even hundreds of amino acids.

Peptides play many important roles in the body, including serving as hormones, neurotransmitters, enzymes, and antibiotics. They are also used in medical research and therapeutic applications, such as drug delivery and tissue engineering.

Pulmonary gas exchange is the process by which oxygen (O2) from inhaled air is transferred to the blood, and carbon dioxide (CO2), a waste product of metabolism, is removed from the blood and exhaled. This process occurs in the lungs, primarily in the alveoli, where the thin walls of the alveoli and capillaries allow for the rapid diffusion of gases between them. The partial pressure gradient between the alveolar air and the blood in the pulmonary capillaries drives this diffusion process. Oxygen-rich blood is then transported to the body's tissues, while CO2-rich blood returns to the lungs to be exhaled.

Physical chemistry is a branch of chemistry that deals with the fundamental principles and laws governing the behavior of matter and energy at the molecular and atomic levels. It combines elements of physics, chemistry, mathematics, and engineering to study the properties, composition, structure, and transformation of matter. Key areas of focus in physical chemistry include thermodynamics, kinetics, quantum mechanics, statistical mechanics, electrochemistry, and spectroscopy.

In essence, physical chemists aim to understand how and why chemical reactions occur, what drives them, and how they can be controlled or predicted. This knowledge is crucial for developing new materials, medicines, energy technologies, and other applications that benefit society.

The amnion is the innermost fetal membrane in mammals, forming a sac that contains and protects the developing embryo and later the fetus within the uterus. It is one of the extraembryonic membranes that are derived from the outer cell mass of the blastocyst during early embryonic development. The amnion is filled with fluid (amniotic fluid) that allows for the freedom of movement and protection of the developing fetus.

The primary function of the amnion is to provide a protective environment for the growing fetus, allowing for expansion and preventing physical damage from outside forces. Additionally, the amniotic fluid serves as a medium for the exchange of waste products and nutrients between the fetal membranes and the placenta. The amnion also contributes to the formation of the umbilical cord and plays a role in the initiation of labor during childbirth.

'Sus scrofa' is the scientific name for the wild boar, a species of suid that is native to much of Eurasia and North Africa. It is not a medical term or concept. If you have any questions related to medical terminology or health-related topics, I would be happy to help with those instead!

Hydrophobic interactions: These are the interactions that occur between non-polar molecules or groups of atoms in an aqueous environment, leading to their association or aggregation. The term "hydrophobic" means "water-fearing" and describes the tendency of non-polar substances to repel water. When non-polar molecules or groups are placed in water, they tend to clump together to minimize contact with the polar water molecules. These interactions are primarily driven by the entropy increase of the system as a whole, rather than energy minimization. Hydrophobic interactions play crucial roles in various biological processes, such as protein folding, membrane formation, and molecular self-assembly.

Hydrophilic interactions: These are the interactions that occur between polar molecules or groups of atoms and water molecules. The term "hydrophilic" means "water-loving" and describes the attraction of polar substances to water. When polar molecules or groups are placed in water, they can form hydrogen bonds with the surrounding water molecules, which helps solvate them. Hydrophilic interactions contribute to the stability and functionality of various biological systems, such as protein structure, ion transport across membranes, and enzyme catalysis.

Photosystem II Protein Complex is a crucial component of the photosynthetic apparatus in plants, algae, and cyanobacteria. It is a multi-subunit protein complex located in the thylakoid membrane of the chloroplasts. Photosystem II plays a vital role in light-dependent reactions of photosynthesis, where it absorbs sunlight and uses its energy to drive the oxidation of water molecules into oxygen, electrons, and protons.

The protein complex consists of several subunits, including the D1 and D2 proteins, which form the reaction center, and several antenna proteins that capture light energy and transfer it to the reaction center. Photosystem II also contains various cofactors, such as pigments (chlorophylls and carotenoids), redox-active metal ions (manganese and calcium), and quinones, which facilitate the charge separation and electron transfer processes during photosynthesis.

Photosystem II Protein Complex is responsible for the initial charge separation event in photosynthesis, which sets off a series of redox reactions that ultimately lead to the reduction of NADP+ to NADPH and the synthesis of ATP, providing energy for the carbon fixation reactions in the Calvin cycle. Additionally, Photosystem II Protein Complex is involved in oxygen evolution, contributing to the Earth's atmosphere's oxygen levels and making it an essential component of global carbon fixation and oxygen production.

Membrane fluidity, in the context of cell biology, refers to the ability of the phospholipid bilayer that makes up the cell membrane to change its structure and organization in response to various factors. The membrane is not a static structure but rather a dynamic one, with its lipids constantly moving and changing position.

Membrane fluidity is determined by the fatty acid composition of the phospholipids that make up the bilayer. Lipids with unsaturated fatty acids have kinks in their hydrocarbon chains, which prevent them from packing closely together and increase membrane fluidity. In contrast, lipids with saturated fatty acids can pack closely together, reducing membrane fluidity.

Membrane fluidity is important for various cellular processes, including the movement of proteins within the membrane, the fusion of vesicles with the membrane during exocytosis and endocytosis, and the ability of the membrane to respond to changes in temperature and other environmental factors. Abnormalities in membrane fluidity have been linked to various diseases, including cancer, neurological disorders, and infectious diseases.

Cholesterol is a type of lipid (fat) molecule that is an essential component of cell membranes and is also used to make certain hormones and vitamins in the body. It is produced by the liver and is also obtained from animal-derived foods such as meat, dairy products, and eggs.

Cholesterol does not mix with blood, so it is transported through the bloodstream by lipoproteins, which are particles made up of both lipids and proteins. There are two main types of lipoproteins that carry cholesterol: low-density lipoproteins (LDL), also known as "bad" cholesterol, and high-density lipoproteins (HDL), also known as "good" cholesterol.

High levels of LDL cholesterol in the blood can lead to a buildup of cholesterol in the walls of the arteries, increasing the risk of heart disease and stroke. On the other hand, high levels of HDL cholesterol are associated with a lower risk of these conditions because HDL helps remove LDL cholesterol from the bloodstream and transport it back to the liver for disposal.

It is important to maintain healthy levels of cholesterol through a balanced diet, regular exercise, and sometimes medication if necessary. Regular screening is also recommended to monitor cholesterol levels and prevent health complications.

"Mannheimia haemolytica" is a gram-negative, rod-shaped bacterium that is commonly found as part of the normal flora in the upper respiratory tract of cattle and other ruminants. However, under certain conditions such as stress, viral infection, or sudden changes in temperature or humidity, the bacteria can multiply rapidly and cause a severe respiratory disease known as shipping fever or pneumonic pasteurellosis.

The bacterium is named "haemolytica" because it produces a toxin that causes hemolysis, or the breakdown of red blood cells, resulting in the characteristic clear zones around colonies grown on blood agar plates. The bacteria can also cause other symptoms such as fever, coughing, difficulty breathing, and depression.

"Mannheimia haemolytica" is a significant pathogen in the cattle industry, causing substantial economic losses due to mortality, reduced growth rates, and decreased milk production. Prevention and control measures include good management practices, vaccination, and prompt treatment of infected animals with antibiotics.

Secondary protein structure refers to the local spatial arrangement of amino acid chains in a protein, typically described as regular repeating patterns held together by hydrogen bonds. The two most common types of secondary structures are the alpha-helix (α-helix) and the beta-pleated sheet (β-sheet). In an α-helix, the polypeptide chain twists around itself in a helical shape, with each backbone atom forming a hydrogen bond with the fourth amino acid residue along the chain. This forms a rigid rod-like structure that is resistant to bending or twisting forces. In β-sheets, adjacent segments of the polypeptide chain run parallel or antiparallel to each other and are connected by hydrogen bonds, forming a pleated sheet-like arrangement. These secondary structures provide the foundation for the formation of tertiary and quaternary protein structures, which determine the overall three-dimensional shape and function of the protein.

Lipopolysaccharides (LPS) are large molecules found in the outer membrane of Gram-negative bacteria. They consist of a hydrophilic polysaccharide called the O-antigen, a core oligosaccharide, and a lipid portion known as Lipid A. The Lipid A component is responsible for the endotoxic activity of LPS, which can trigger a powerful immune response in animals, including humans. This response can lead to symptoms such as fever, inflammation, and septic shock, especially when large amounts of LPS are introduced into the bloodstream.

Uteroglobin, also known as blastokinin or Clara cell 10-kDa protein (CC10), is a small molecular weight protein that is abundantly present in the respiratory tract and reproductive system of many mammals. It was first identified in the uterine fluid of pregnant animals, hence its name.

In the human body, uteroglobin is primarily produced by non-ciliated bronchial epithelial cells known as Clara cells, which are located in the respiratory tract. Uteroglobin has been found to have anti-inflammatory and immunomodulatory properties, and it may play a role in protecting the lungs from injury and inflammation.

In the reproductive system, uteroglobin is produced by the endometrial glands of the uterus during pregnancy, and it has been suggested to have a role in maintaining pregnancy and promoting fetal growth. However, its precise functions in both the respiratory and reproductive systems are not fully understood and are still the subject of ongoing research.

Dexamethasone is a type of corticosteroid medication, which is a synthetic version of a natural hormone produced by the adrenal glands. It is often used to reduce inflammation and suppress the immune system in a variety of medical conditions, including allergies, asthma, rheumatoid arthritis, and certain skin conditions.

Dexamethasone works by binding to specific receptors in cells, which triggers a range of anti-inflammatory effects. These include reducing the production of chemicals that cause inflammation, suppressing the activity of immune cells, and stabilizing cell membranes.

In addition to its anti-inflammatory effects, dexamethasone can also be used to treat other medical conditions, such as certain types of cancer, brain swelling, and adrenal insufficiency. It is available in a variety of forms, including tablets, liquids, creams, and injectable solutions.

Like all medications, dexamethasone can have side effects, particularly if used for long periods of time or at high doses. These may include mood changes, increased appetite, weight gain, acne, thinning skin, easy bruising, and an increased risk of infections. It is important to follow the instructions of a healthcare provider when taking dexamethasone to minimize the risk of side effects.

Fatty alcohols, also known as long-chain alcohols or long-chain fatty alcohols, are a type of fatty compound that contains a hydroxyl group (-OH) and a long alkyl chain. They are typically derived from natural sources such as plant and animal fats and oils, and can also be synthetically produced.

Fatty alcohols can vary in chain length, typically containing between 8 and 30 carbon atoms. They are commonly used in a variety of industrial and consumer products, including detergents, emulsifiers, lubricants, and personal care products. In the medical field, fatty alcohols may be used as ingredients in certain medications or topical treatments.

... (SP-D) is a protein domain predominantly found in lung surfactant. This protein plays a special ... Pulmonary surfactant protein D (SP-D), has an important role in acting as a lung host defence protein. SP-D has a significant ... June 2001). "The amino-terminal heptad repeats of the coiled-coil neck domain of pulmonary surfactant protein d are necessary ... March 2006). "Surfactant proteins SP-A and SP-D: structure, function and receptors". Molecular Immunology. 43 (9): 1293-315. ...
... is a surface-active complex of phospholipids and proteins formed by type II alveolar cells. The proteins ... of the surfactant. Half of this 10% is plasma proteins but the rest is formed by the apolipoproteins, surfactant proteins SP-A ... Surfactant immune function is primarily attributed to two proteins: SP-A and SP-D. These proteins can bind to sugars on the ... The DPPC is the strongest surfactant molecule in the pulmonary surfactant mixture. It also has a higher compaction capacity ...
... (SP-A2), also known as Pulmonary surfactant-associated protein A2 (PSP-A2) is a protein that in humans is ... Together with (surfactant protein A1 ) SP-A1, they are the most abundant proteins of pulmonary surfactant. SP-A2 binds to the ... "Assignment of the human pulmonary surfactant protein D gene (SFTP4) to 10q22-q23 close to the surfactant protein A gene cluster ... "Surfactant protein A2 mutations associated with pulmonary fibrosis lead to protein instability and endoplasmic reticulum stress ...
"Assignment of the human pulmonary surfactant protein D gene (SFTP4) to 10q22-q23 close to the surfactant protein A gene cluster ... Surfactant protein D, also known as SP-D, is a lung surfactant protein part of the collagenous family of proteins called ... "Entrez Gene: SFTPD surfactant, pulmonary-associated protein D". Brandt EB, Mingler MK, Stevenson MD, Wang N, Khurana Hershey GK ... Zhang L, Ikegami M, Crouch EC, Korfhagen TR, Whitsett JA (June 2001). "Activity of pulmonary surfactant protein-D (SP-D) in ...
... is an essential lipid-associated protein found in pulmonary surfactant. Without it, the lung would not be ... the other three being surfactant protein A (SP-A), surfactant protein C (SP-C), and surfactant protein D (SP-D). These four are ... SP-B is a critical protein for lung function, and is found in the context of pulmonary surfactant. Understanding surfactant is ... Surfactant protein B (SP-B) is a small protein, weighing about 8 kDa. Proteins are composed of building blocks called amino ...
... (SP-C), is one of the pulmonary surfactant proteins. In humans this is encoded by the SFTPC gene. It is a ... GeneReviews/NIH/NCBI/UW entry on Pulmonary Fibrosis, Familial Pulmonary+Surfactant-Associated+Protein+B at the U.S. National ... "The pulmonary surfactant protein C (SP-C) precursor is a type II transmembrane protein". The Biochemical Journal. 277 ( Pt 2) ( ... "Entrez Gene: SFTPC surfactant, pulmonary-associated protein C". Willander H, Askarieh G, Landreh M, Westermark P, Nordling K, ...
... (SP-A1), also known as Pulmonary surfactant-associated protein A1 (PSP-A) is a protein that in humans is ... "Assignment of the human pulmonary surfactant protein D gene (SFTP4) to 10q22-q23 close to the surfactant protein A gene cluster ... Surfactant protein A1". Silveyra P, Floros J (Dec 2013). "Genetic complexity of the human surfactant-associated proteins SP-A1 ... Together with SP-A2, they are the most abundant proteins of pulmonary surfactant. SP-A1 binds to the carbohydrates found in the ...
Wang, J Y; C C Shieh; P F You; H Y Lei; K B Reid (August 1998). "Inhibitory effect of pulmonary surfactant proteins A and D on ... surfactant protein A SP-D = surfactant protein D CL-L1 = collectin liver 1 CL-P1 = collectin placenta 1 CL-43 = Collectin of 43 ... Crouch, E; J R Wright (2001). "Surfactant proteins a and d and pulmonary host defense". Annual Review of Physiology. 63: 521- ... "Pulmonary surfactant proteins A and D enhance neutrophil uptake of bacteria". The American Journal of Physiology. 274 (6 Pt 1 ...
pulmonary surfactant SFTPA1 SFTPA2 Surfactant+Protein+A at the U.S. National Library of Medicine Medical Subject Headings (MeSH ... van Iwaarden F, Welmers B, Verhoef J, Haagsman HP, van Golde LM (January 1990). "Pulmonary surfactant protein A enhances the ... Surfactant protein A is an innate immune system collectin. It is water-soluble and has collagen-like domains similar to SP-D. ... The role of surfactant protein A (SP-A) in childbirth is indicated in studies with mice. Mice which gestate for 19 days ...
Genetic associations include mutations in pulmonary surfactant proteins A1, A2, C (SFTPA1, SFTPA2B) and mucin (MUC5B). A ... The number of published studies on the role of pulmonary rehabilitation in idiopathic pulmonary fibrosis is small, but most of ... "Idiopathic Pulmonary Fibrosis". NHLBI, NIH. Retrieved 5 December 2020. Meltzer EB, Noble PW (2008). "Idiopathic pulmonary ... December 2011). "Familial pulmonary fibrosis is the strongest risk factor for idiopathic pulmonary fibrosis". Respiratory ...
Exon structure reveals its evolutionary relationship to a human pulmonary surfactant gene and localization to chromosome 10". J ... the MASP protein functions to cleave the blood protein C4 into C4a and C4b. The C4b fragments can then bind to the surface of ... "Mannose-binding protein C precursor [Homo sapiens]". Retrieved 2012-01-03. Jensen PH, Laursen I, Matthiesen F, Højrup P (2007 ... It is produced in the liver as a response to infection, and is part of many other factors termed acute phase proteins. ...
... amphipathic peptoid mimics of pulmonary surfactant proteins". Scientific Reports. 8 (1): 6795. doi:10.1038/s41598-018-25009-3. ... Brown NJ, Johansson J, Barron AE (October 2008). "Biomimicry of surfactant protein C". Accounts of Chemical Research. 41 (10): ... synthetic lung surfactants, ligands for various proteins including Src Homology 3 (SH3 domain), Vascular Endothelial Growth ... Peptoids were first invented by Reyna J. Simon, Ronald N. Zuckermann, Paul Bartlett and Daniel V. Santi to mimic protein/ ...
... with type II cells producing pulmonary surfactant covering around 2% of the alveolar walls. Once surfactant is secreted by the ... "Interaction of the lipid and protein components of pulmonarysurfactant Role of phosphatidylglycerol and calcium". Biochimica et ... Phosphatidylglycerol is a glycerophospholipid found in pulmonary surfactant and in the plasma membrane where it directly ... of pulmonary surfactant phospholipids. It is synthesized by head group exchange of a phosphatidylcholine enriched phospholipid ...
Pulmonary surfactants can be classified into three types: The first generation of protein-free synthetic surfactants contained ... where DPPC interacts with surfactant proteins to form pulmonary surfactant. Current studies cannot find a correlation between ... Pulmonary surfactant has both protein and lipid components. More specifically, it has been found that phosphatidylcholine (PC) ... Surfactant Dysfunction Disorder is a disease that affects newborn children whose pulmonary surfactant is insufficient for ...
The ACADL gene has also been linked to pathophysiology of pulmonary disease. In humans, this protein was shown to be localized ... Mice that were lacking LCAD (-/-) had dysfunctional or reduced amounts of pulmonary surfactant, which is required to prevent ... "Long-chain acyl-CoA dehydrogenase deficiency as a cause of pulmonary surfactant dysfunction". The Journal of Biological ... Acyl-CoA dehydrogenase, long chain is a protein that in humans is encoded by the ACADL gene. ACADL is a gene that encodes LCAD ...
... and hydrophobic proteins that carry out physical functions of pulmonary surfactant. Surfactant metabolism dysfunction involves ... Severe deficiency of pulmonary surfactant due to disturbed metabolism of any of these proteins can lead to some form of ... Surfactant is classified into two types of proteins, hydrophilic proteins that are responsible for innate immune system, ... Surfactant metabolism dysfunction is a condition where pulmonary surfactant is insufficient for adequate respiration. Surface ...
SFTPB is released into the pulmonary surfactant, playing a role in rearranging lipids. However, proteins like GNLY and AOAH do ... Hawgood S, Derrick M, Poulain F (Nov 1998). "Structure and properties of surfactant protein B". Biochimica et Biophysica Acta ( ... The saposin domains refers to two evolutionally-conserved protein domains found in saposin and related proteins (SAPLIP). ... Protein domains, Protein families, Peripheral membrane proteins). ...
In particular, she evaluates the structure and function of the key proteins that compose the pulmonary surfactant system and ... of the pulmonary surfactant protein SP-D can acquire significant anti-viral properties by enhancing the binding of the protein ... Minkara's research uses computational methods to provide insight into the complex nature of the pulmonary surfactant system. ... to the trimannose molecule that mediates the interaction of the protein and the virus. Minkara leads the COMBINE lab at ...
The secretion, called pulmonary surfactant, reduces surface tension, allowing for bronchioles to expand during inspiration and ... Club cells are non-ciliated, rounded protein-secreting cells. Their secretions are a non-sticky, proteinaceous compound to ... The pulmonary lobule is the portion of the lung ventilated by one bronchiole. Bronchioles are approximately 1 mm or less in ... chronic obstructive pulmonary disease (COPD), and chronic bronchitis. The trachea divides into the left main bronchus which ...
... and a solution similar in composition to pulmonary surfactant. They are also responsible for detoxifying harmful substances ... "Clara cell secretory protein" were conclusively replaced with "club cell" and "club cell secretory protein", respectively. cGMP ... When the l7Rn6 protein is disrupted in mice, these mice display severe emphysema at birth as a result of disorganization of the ... Serum club cell proteins are used as a biomarker of lung permeability. Exposure to particulate air pollution may compromise the ...
... is a major constituent of cell membranes and pulmonary surfactant, and is more commonly found in the ... "Interacting proteins dictate function of the minimal START domain phosphatidylcholine transfer protein/StarD2". The Journal of ... Dipalmitoylphosphatidylcholine (lecithin) is a major component of the pulmonary surfactant, and is often used in the lecithin- ... Wirtz KW (July 1991). "Phospholipid transfer proteins". Annual Review of Biochemistry. 60 (13): 73-99. doi:10.1146/annurev.bi. ...
Long term exposure to dust particles containing metallic compounds have been found to impair pulmonary surfactant and lung ... An increase of dust levels have had negative health effects on employees as found in their serum protein levels, respiratory, ... An increase in 5 neurology-related proteins were found (GCSF, EFNA4, CTSS, CLM6, VEC2) in welder's blood. Constant changes in ... 2020). "Exposure to Mild Steel Welding and Changes in Serum Proteins With Putative Neurological Function-A Longitudinal Study ...
Soon enough, part of the vernix is emulsified by increasing concentrations of pulmonary surfactants and desiccates, only to be ... The protein composition is relatively understudied. Vernix of term infants has more squalene and a higher wax ester to sterol ... Chemically, it is water (80%), lipids (10%) and proteins (10%). The lipids include ceramides, cholesterol, fatty acids, ...
... pulmonary surfactant-associated protein B (pulmonary surfactant regulation) and the saposins (sphingolipid degradation) of ... "Conformational mapping of the N-terminal segment of surfactant protein B in lipid using 13C-enhanced Fourier transform infrared ... is homologous to saposin and belongs to the saposin-like protein family (SAPLIP). Although the PSI is grouped along proteins in ... The underlying function of proteins belonging to the SAPLIP group is to interact with membrane bilayers, either by perturbation ...
... pulmonary surfactant-associated protein a MeSH D12.776.503.280.249.625 - pulmonary surfactant-associated protein d MeSH D12.776 ... groel protein MeSH D12.776.602.500.500.100 - fusion proteins, bcr-abl MeSH D12.776.602.500.500.320 - fusion proteins, gag-onc ... oncogene protein v-maf MeSH D12.776.964.700.750.875 - oncogene proteins v-abl MeSH D12.776.964.700.750.882 - oncogene proteins ... fusion proteins, gag-pol MeSH D12.776.964.775.350.400 - hiv core protein p24 MeSH D12.776.964.775.375.325 - fusion proteins, ...
... , also known by the trade name of Survanta, is a modified bovine pulmonary surfactant containing bovine lung extract ( ... and bovine surfactant proteins), to which synthetic DPPC, tripalmitin and palmitic acid are added. The composition provides 25 ...
Pulmonary surfactant is a complex system of lipids, proteins and glycoproteins that is produced in specialized lung cells ... Bubble CPAP Bronchopulmonary dysplasia Pulmonary hypoplasia Surfactant metabolism dysfunction Surfactant therapy Wilson-Mikity ... For the S/A ratio, the result is given as milligrams of surfactant per gram of protein. A S/A ratio less than 35 indicates ... An exogenous preparation of pulmonary surfactant, either synthetic or extracted from animal lungs, is given through the ...
... major coat protein Pilin Pulmonary surfactant-associated protein Monoamine oxidases A and B Fatty acid amide hydrolase ... In humans, 27% of all proteins have been estimated to be alpha-helical membrane proteins. Beta-barrel proteins are so far found ... A transmembrane protein (TP) is a type of integral membrane protein that spans the entirety of the cell membrane. Many ... Membrane Proteins of known 3D Structure Elofsson, Arne; Heijne, Gunnar von (7 June 2007). "Membrane Protein Structure: ...
... interacting protein (liprin), alpha 1 Protocadherin alpha 1 Pulmonary surfactant-associated protein A1 Pyruvate dehydrogenase ( ... lipoamide) alpha 1 RNA binding motif protein, Y-linked, family 1, member A1 Replication protein A1 S100 calcium binding protein ... This is a list of genes, proteins or receptors named A1 or Alpha-1 : Actin, alpha 1 Actinin, alpha 1 Adaptor-related protein ... an acute-phase protein in the Alpha 1-antitrypsin deficiency, a genetic disorder Annexin A1, a human protein Outer membrane ...
... for example in development surfactants, foams and emulsions. Many biological systems like pulmonary surfactant and meibum are ... Surfactants and surface active polymers used are for stabilising emulsions and foams in food and cosmetic industries. Proteins ... and has helped to develop therapies like artificial pulmonary surfactant replacements and eye drops. Interfacial rheology ... When surfactants are present in a liquid, they tend to adsorb in the liquid-air or liquid-liquid interface. Interfacial ...
Pulmonary surfactant protein D (SP-D) is a protein domain predominantly found in lung surfactant. This protein plays a special ... Pulmonary surfactant protein D (SP-D), has an important role in acting as a lung host defence protein. SP-D has a significant ... June 2001). "The amino-terminal heptad repeats of the coiled-coil neck domain of pulmonary surfactant protein d are necessary ... March 2006). "Surfactant proteins SP-A and SP-D: structure, function and receptors". Molecular Immunology. 43 (9): 1293-315. ...
Pulmonary Surfactant-Associated Protein A/genetics/*metabolism, Pulmonary Surfactant-Associated Protein B/genetics/*metabolism, ... Pulmonary surfactant protein A, B, and C mRNA and protein expression in the nitrofen-induced congenital diaphragmatic hernia ... Pulmonary Surfactant-Associated Protein C/genetics/*metabolism, RNA, Messenger/*metabolism, Rats, Rats, Wistar, Research ... In this study, we tested the possibility that CDH lungs are surfactant protein deficient, which could explain the respiratory ...
We have isolated a surfactant-associated protein complex with molecular weight components of 36 000, 32 000, and 28 000 an … ... Previous studies have demonstrated that lung-specific proteins are associated with surfactant lipids, particularly the highly ... Proteins / isolation & purification * Proteins / metabolism* * Pulmonary Surfactants / isolation & purification * Pulmonary ... Effects of a surfactant-associated protein and calcium ions on the structure and surface activity of lung surfactant lipids ...
Mutations in the surfactant protein C (SP-C) gene (SFTPC) are associated with familial desquamative and nonspecific ... Familial pulmonary fibrosis is a heterogeneous group of interstitial lung diseases of unknown cause that is associated with ... Familial pulmonary fibrosis is a heterogeneous group of interstitial lung diseases of unknown cause that is associated with ... Mutations in the surfactant protein C (SP-C) gene (SFTPC) are associated with familial desquamative and nonspecific ...
Ask ELISA Kit for Bovine Pulmonary Surfactant Associated Protein C(SP-C). ... Related article about: ELISA Kit for Bovine Pulmonary Surfactant Associated Protein C(SP-C) ... ELISA Kit for Human Nuclear Matrix Protein 22(NMP22) ELISA Kit for Human Nuclear Mitotic Apparatus Protein 1(NUMA1) ELISA Kit ... ELISA Kit for Human Nucleolar Protein 1(NOL1) ELISA Kit for Human Nucleolin(NCL) ELISA Kit for Human Nucleophosmin(NPM1) ELISA ...
... stain-positive phospholipoprotein that is derived from surfactant. The lung architecture is otherwise normal, and any ... Pulmonary alveolar proteinosis (PAP) is a rare, diffuse lung disease that is characterized by the alveolar and interstitial ... Surfactant proteins in pulmonary alveolar proteinosis in adults. Eur Respir J. 2004 Sep. 24(3):426-35. [QxMD MEDLINE Link]. [ ... encoded search term (Pulmonary Alveolar Proteinosis Imaging) and Pulmonary Alveolar Proteinosis Imaging What to Read Next on ...
Firstly, the pulmonary surfactant proteins (e.g. SP-A and SP-B) would bind to carbon nanomaterials in the lungs. The complexes ... According to previous reports, the pulmonary surfactant proteins (e.g., SP-A and SP-B) can be bonded to COOH/OH on the surfaces ... The binding of pulmonary surfactant proteins (SP-A or SP-B) to NDs could promote their clearance rate from the lungs [19]. NDs ... Binding of pulmonary surfactant proteins to carbon nanotubes; potential for damage to lung immune defense mechanisms. Carbon ...
Rat SP-D (Pulmonary surfactant-associated protein D) ELISA Kit , G-EC-05617 Rat SP-D (Pulmonary surfactant-associated protein D ... Rat SP-D (Pulmonary surfactant-associated protein D) ELISA Kit , G-EC-05617 ... Mouse SP-D (Pulmonary surfactant-associated protein D) ELISA Kit , G-EC-04660 ... Human SP-D (Pulmonary surfactant-associated protein D) ELISA Kit , G-EC-02962 ...
Regulation and function of pulmonary surfactant protein B.﻽. Pryhuber GS. Molecular genetics and metabolism.. 1998 August 64 (4 ... G-protein-coupled receptor kinase interacting protein-1 is required for pulmonary vascular development.﻽. Pang J, Hoefen R, ... Regulation of surfactant proteins A and B by TNF-alpha and phorbol ester independent of NF-kappa B.﻽. Pryhuber GS, Khalak R, ... Regulation of surfactant proteins A and B by TNF-? and phorbol ester independent of NF-?B.﻽. Pryhuber GS, Khalak R, Zhao Q ...
Surfactant is produced by alveolar type II cells which can be differentiated in vitro from patient specific induced pluripotent ... We also show the presence of normal lamellar bodies and the secretion of surfactant into the cell culture medium in the ... we show expression of SFTPB mRNA during endodermal and organoid differentiation but the protein product only after organoid ... Surfactant protein B (SFTPB) deficiency is a fatal disease affecting newborn infants. ...
PDB Compounds: (B:) Pulmonary surfactant-associated protein D. SCOPe Domain Sequences for d2orkb2:. Sequence; same for both ... PDB Description: crystal structure of the trimeric neck and carbohydrate recognition domain of human surfactant protein D in ... d2orkb2 h.1.1.1 (B:205-234) Surfactant protein {Human (Homo sapiens), SP-D [TaxId: 9606]} aslrqqvealqgqvqhlqaafsqykkvelf SCOPe ... Class h: Coiled coil proteins [57942] (7 folds). *. Fold h.1: Parallel coiled-coil [57943] (41 superfamilies). this is not a ...
Mannose-Binding Protein A, subunit A Functional Family. Pulmonary surfactant-associated protein D ... High resolution structural insights into ligand binding and immune cell recognition by human lung surfactant protein D ... CATH: Protein Structure Classification Database by I. Sillitoe, N. Dawson, T. Lewis, D. Lee, J. Lees, C. Orengo is licensed ...
The Porcine Pulmonary Surfactant Protein A (pSP-A) Immunogenicity Evaluation in the Murine Model (Articles) ...
It is a syndrome characterized by marked pulmonary hypertension that causes hypoxemia and right-to-left intracardiac shunting ... Persistent pulmonary hypertension of the newborn (PPHN) is defined as the failure of the normal circulatory transition that ... genetic mutations leading to surfactant protein B deficiency, and mutations in the ATP-binding cassette transporter 3 gene. [4 ... Hypoplasia of the pulmonary vascular bed. Hypoplasia of the pulmonary vascular bed is another cause of persistent pulmonary ...
Surfactant dysfunction is a lung disorder that causes breathing problems. Explore symptoms, inheritance, genetics of this ... and surfactant protein-C (SP-C), respectively, two of the four proteins in surfactant. These two proteins help spread the ... An overview of pulmonary surfactant in the neonate: genetics, metabolism, and the role of surfactant in health and disease. Mol ... Hamvas A. Inherited surfactant protein-B deficiency and surfactant protein-C associated disease: clinical features and ...
Pulmonary surfactant protein A (SP-A), a heterooligomer of SP-A1 and SP-A2, is an important regulator of innate immunity of the ... Identification and Quantitation of Coding Variants and Isoforms of Pulmonary Surfactant Protein A ... Ledfords current work in the area of pulmonary surfactant immunobiology combines her knowledge of mouse genetics, pulmonary ... Identification and Quantitation of Coding Variants and Isoforms of Pulmonary Surfactant Protein A. Journal of proteome research ...
Effects on pulmonary surfactant secretion were assessed through changes in phospholipid content of the lavagate. Phosgene alone ... Lung lavage fluid was used for neutrophil counts and protein concentration determinations. Changes in alveolar/capillary ... Colchicine inhibits elevations in both alveolar-capillary membrane permeability and lavage surfactant after exposure of the rat ... NIOSH-Publication; NIOSH-Grant; Pulmonary-system-disorders; Drugs; Toxic-gases; Organo-chlorine-compounds; In-vivo-studies; ...
Protein Name. Pulmonary surfactant-associated protein B. Description of Target. SFTPB is the pulmonary-associated surfactant B ... The SFTPB gene encodes the pulmonary-associated surfactant B protein (SPB), an amphipathic surfactant protein essential for ... protein (SPB), an amphipathic surfactant protein essential for lung function and homeostasis after birth. Pulmonary surfactant ... What protein functions are associated with "SFTPB"?. This protein has been associated with "Protein Functions". Please view the ...
Pulmonary surfactant mainly consists of phospholipids (approximately 90 %) and four specific surfactant proteins (SP-A, SP-B, ... Pulmonary Surfactant. While the thiol group on glutathione is the primary reactant for isocyanate, there is also evidence that ... The airway and alveolar lining fluid is an aqueous buffer containing surfactant (phospholipids), protein, and various ... MDI will interact with pulmonary surfactant present in the lung fluid. While the primary role of the surfactant is to reduce ...
Pulmonary surfactant, also known as lung surfactant, is a detergent-like, lipid-protein mixture synthesized by alveolar type II ... Heat shock protein 90 (Hsp90) is a master chaperone, regulating processes involved in cell cycle control, protein folding, and ... A proteins natively folded state, as we call it, may or may not be an energy-minimized state. It can very well be a state with ... bps1526 career advice25 presentation23 stem16 students14 nih13 funding12 Philadelphia12 science policy12 Proteins11 disease ...
Mouse SP-A1 (Pulmonary surfactant-associated protein A1) CLIA Kit , G-EC-01626 ... Mouse SPD (Pulmonary Surfactant Associated Protein D) CLIA Kit , G-EC-01627 ... Mouse MAPÏ„ (Microtubule Associated Protein Tau/Tau Protein) CLIA Kit , G-EC-01658 ... Mouse BFP (Brain Finger Protein) CLIA Kit , G-EC-01705 Mouse BFP (Brain Finger Protein) CLIA Kit , G-EC-01705 , Gentaur Clia ...
3 People Results for the Tag: Pulmonary Surfactant Associated Protein A. .remove { display: block; cursor: pointer; float: ...
Next are patients with genetic mutations in: surfactant protein B (SFTPB), ABCA3, surfactant protein C (SFTPC) and pulmonary ... pulmonary fibrosis, disorders of surfactant homeostasis (figure 1), asthma, chronic obstructive lung disease (COPD) and cystic ... Division of Pulmonary Biology. 3333 Burnet Ave. Cincinnati, OH 45229-3039. Phone: 513-803-2790. Email: [email protected] ... Assess mechanisms controlling surfactant homeostasis at the cellular and molecular level Educational Opportunities. *PhD and MD ...
i,Objective.,/i, To determine the correlation between maternal bile acid (BA) level and fetal pulmonary surfactant in rats and ... H. Maeda, M. Q. Fujita, B.-L. Zhu et al., "Pulmonary surfactant-associated protein A as a marker of respiratory distress in ... I. R. Doyle, T. E. Nicholas, and A. D. Bersten, "Serum surfactant protein-A levels in patients with acute cardiogenic pulmonary ... SP-A acts as a pulmonary surfactant binding protein and is secreted by type II pneumonocyte. When the lung is damaged, the ...
Surfactant protein A. Surfactant protein A is an innate immune system collectin.- During Parturition :The role of Surfactant ... Proteins. Proteins make up the remaining 10% of the surfactant. Half of this 10% is plasma proteins but the rest is formed by ... Mini review on Pulmonary Surfactant Minireview covering composition, function and pathologies of Pulmonary Surfactant ... Artificial surfactants. Synthetic pulmonary surfactants * Exosurf - a mixture of DPPC with hexadecanol and tyloxapol added as ...
Pulmonary surfactant is mainly composed of phospholipids and minor amounts of other lipids and specific proteins. Surfactant ... "Decreased surfactant lipids correlate with lung function in chronic obstructive pulmonary disease (COPD) PLoS One 15(2) ... In the lab, we use cell culture and in vivo models to study the regulation of surfactant homeostasis and its dysregulation ... Pulmonary metabolism in smoke-related disease. Icahn School of Medicine at Mount Sinai, New York (2014-2015) ...
... that could be used in development of a sputum test for early detection of chronic obstructive pulmonary disease (COPD). That ... Proteomics of Human Lung Tissue Identifies Surfactant Protein A as a Marker of Chronic Obstructive Pulmonary Disease. Journal ... Past research pointed to a prime candidate - surfactant protein A (SP-A), which has a major role in fighting infections and ... Advance Toward Early Diagnosis Of Chronic Obstructive Pulmonary Disease. Date:. December 17, 2008. Source:. American Chemical ...
Surfactant protein C mutations and familial pulmonary fibrosis: stuck in a loop on the scenic route European Respiratory ... Doveston RG Cooperative stabilisation of 14-3-3σ protein-protein interactions via covalent protein modification Chemical ... Discovering protein-protein interaction stabilisers by native mass spectrometry Chemical Science 12: 10724-10731 ... Thurairajah B, Hudson AJ Doveston RG Contemporary biophysical approaches for studying 14-3-3 protein-protein interactions Front ...
Surfactant protein A (SP-A) is the major protein component of pulmonary surfactant, a material secreted by the alveolar type II ... Immunomodulatory functions of surfactant. Wright, J.R. Physiol. Rev. (1997) [Pubmed]. *Pulmonary surfactant protein B (SP-B): ... SP-B is a protein in pulmonary surfactant that is, in greatest part, responsible for resistance to surface tension and ... The role of pulmonary collectin N-terminal domains in surfactant structure, function, and homeostasis in vivo. Palaniyar, N., ...
Pulmonary surfactant-associated protein A1. MWLCPLALNLILMAASGAVCEVKDVCVGSPGIPGTPGSHGLPGRDGRDGL.... unknown. Manganese catalase ... Tyrosine-protein kinase transforming protein Abl. YITPVNSLEKHSWYHGPVSRNAAEYLLSSGINGSFLVRESESSPGQRSIS.... unknown. Bifunctional ... Hypothetical gliding protein. MVEPSLVLYGAPYERAVEVLEETLRETGARYALLIDRKGFVLAHKEALWA.... unknown. Prolyl endopeptidase Pep. ... Thiol:disulfide interchange protein DsbC. MKKGFMLFTLLAAFSGFAQADDAAIQQTLAKMGIKSSDIQPAPVAGMKTV.... unknown. Glyceraldehyde-3- ...
  • Previous studies have demonstrated that lung-specific proteins are associated with surfactant lipids, particularly the highly surface active subfraction known as tubular myelin. (nih.gov)
  • We have isolated a surfactant-associated protein complex with molecular weight components of 36 000, 32 000, and 28 000 and reassembled it with protein-free lung surfactant lipids prepared as small unilamellar liposomes. (nih.gov)
  • The effects of divalent cations on the structure and surface activity of this protein-lipid mixture were investigated by following (1) the state of lipid dispersion by changes in turbidity and by electron microscopy and (2) the ability of the surfactant lipids to form a surface film from an aqueous subphase at 37 degrees C. The protein complex markedly increased the rate of Ca2+-induced surfactant-lipid aggregation. (nih.gov)
  • Similarly, 5 mM Ca2+ but not 5 mM Mg2+ improved the ability of the protein-lipid mixture to form a surface film at 37 degrees C. Extensive aggregation of the surfactant lipids without protein by 20 mM Ca2+ or 20 mM Mg2+ did not promote rapid surface film formation. (nih.gov)
  • Pulmonary surfactant is mainly composed of phospholipids and minor amounts of other lipids and specific proteins. (downstate.edu)
  • A delicate balance between synthesis, secretion, recycling and degradation of the lipids is required to maintain surfactant function and lung performance. (downstate.edu)
  • Samaha G., Garcia-Arcos I., (2020) "Alveolar lipids in pulmonary disease. (downstate.edu)
  • The saposin B-type domain is a ~80 amino acid domain present in saposins and related proteins that interact with lipids. (embl.de)
  • At this interface, proteins and lipids of the pulmonary surfactant bind to MWCNTs, affecting their surface characteristics. (biomedcentral.com)
  • In preterm infants, surfactant replacement therapies that include lipids and the hydrophobic surfactant proteins are highly efficacious in improving lung function. (fz-borstel.de)
  • Familial pulmonary fibrosis is a heterogeneous group of interstitial lung diseases of unknown cause that is associated with multiple pathologic subsets. (nih.gov)
  • A transversion of SFTPC in a large familial pulmonary fibrosis kindred, including adults with usual interstitial pneumonitis and children with cellular nonspecific interstitial pneumonitis. (nih.gov)
  • We show that an SFTPC mutation segregates with the pulmonary fibrosis phenotype in this kindred and may cause type II cellular injury. (nih.gov)
  • The scientists compared levels of a variety of proteins obtained from the lung tissues of healthy individuals, patients with COPD, and those with pulmonary fibrosis. (sciencedaily.com)
  • Targeted AntiBiotics for Chronic pulmonary diseases (TARGET ABC): can targeted antibiotic therapy improve the prognosis of Pseudomonas aeruginosa-infected patients with chronic pulmonary obstructive disease, non-cystic fibrosis bronchiectasis, and asthma? (sdu.dk)
  • Genetic variants associated with susceptibility to idiopathic pulmonary fibrosis in people of European ancestry: a genome-wide association study. (nature.com)
  • Single-cell deconvolution of fibroblast heterogeneity in mouse pulmonary fibrosis. (nature.com)
  • Single-cell transcriptomic analysis of human lung provides insights into the pathobiology of pulmonary fibrosis. (nature.com)
  • Single-cell RNA sequencing identifies diverse roles of epithelial cells in idiopathic pulmonary fibrosis. (nature.com)
  • We evaluated whether lysyl oxidase-like 2 (LOXL2), which promotes cross-linking of collagen in pathological stroma, was detectable in serum from idiopathic pulmonary fibrosis (IPF) patients, and assessed its relationship with IPF disease progression. (ersjournals.com)
  • Idiopathic pulmonary fibrosis (IPF) is a progressive and ultimately fatal disease of the lungs involving airway epithelial cell damage, fibroblast activation and proliferation, and excessive deposition of collagen and other extracellular matrix (ECM) components [ 1 ]. (ersjournals.com)
  • PD-L1 on invasive fibroblasts drives fibrosis in a humanized model of idiopathic pulmonary fibrosis. (cedars-sinai.edu)
  • Hyaluronan and TLR4 promote surfactant-protein-C-positive alveolar progenitor cell renewal and prevent severe pulmonary fibrosis in mice. (cedars-sinai.edu)
  • This condition results from abnormalities in the composition or function of surfactant, a mixture of certain fats (called phospholipids) and proteins that lines the lung tissue and makes breathing easy. (medlineplus.gov)
  • The phospholipids and proteins that make up surfactant are packaged in cellular structures known as lamellar bodies. (medlineplus.gov)
  • Surfactant is composed of phospholipids and other surfactant-associated proteins. (avivasysbio.com)
  • These include the generation of a variety of lipid mediators, along with membrane remodelling, modification of extracellular non-cellular phospholipid components of pulmonary surfactant, microparticles and lipoproteins, and degradation of microbial membranes and dietary phospholipids. (ijbs.com)
  • Description: A sandwich ELISA kit for detection of Surfactant Associated Protein C from Rat in samples from blood, serum, plasma, cell culture fluid and other biological fluids. (stemcellcharter.org)
  • Idiopathic persistent pulmonary hypertension of the newborn can present without signs of acute perinatal distress. (medscape.com)
  • Without normal surfactant, the tissue surrounding the air sacs in the lungs (the alveoli) sticks together (because of a force called surface tension) after exhalation, causing the alveoli to collapse. (medlineplus.gov)
  • These two proteins help spread the surfactant across the surface of the lung tissue, aiding in the surface tension-lowering property of surfactant. (medlineplus.gov)
  • The loss of functional surfactant raises surface tension in the alveoli, causing severe breathing problems. (medlineplus.gov)
  • Pulmonary surfactant is a lipid-rich material that prevents lung collapse by lowering surface tension at the air-liquid interface in the alveoli of lung. (avivasysbio.com)
  • The major biophysical function of this lung surfactant film is to reduce the alveolar surface tension to near-zero value. (biophysics.org)
  • Surfactants are compounds that lower the surface tension of a liquid, the interfacial tension between two liquids, or that between a liquid and a solid. (absoluteastronomy.com)
  • It is also the only surface active component of lung surfactant capable of lowering surface tension to near zero levels. (absoluteastronomy.com)
  • SP-A is covered on the alveolus surface to decrease the surface tension, thus prevent alveolus collapse, and stabilize pulmonary alveolar pressure [ 9 ]. (hindawi.com)
  • Surfactant allows the lungs to inflate by decreasing the alveolar surface tension and the work needed for inspiration in each breathing cycle. (downstate.edu)
  • Type II cells secrete pulmonary surfactant (a phospholipid bound to a protein) that reduces the surface tension of the moisture that covers the alveolar walls. (cliffsnotes.com)
  • We also show the presence of normal lamellar bodies and the secretion of surfactant into the cell culture medium in the organoids of lentiviral infected cells. (nature.com)
  • Effects on pulmonary surfactant secretion were assessed through changes in phospholipid content of the lavagate. (cdc.gov)
  • Phosgene also caused significant increases in alveolar/capillary membrane permeability immediately after exposure and significant increases in pulmonary surfactant secretion 24 to 26 hours postexposure. (cdc.gov)
  • Adaptation to air breathing after birth is dependent upon the synthesis and secretion of pulmonary surfactant by alveolar type 2 (AT2) cells. (stanford.edu)
  • Alveolar type II (ATII) epithelial cells synthesize, secrete and recycle all components of surfactant and dysfunction in surfactant metabolism can result in a variety of pediatric lung diseases including respiratory distress syndrome and interstitial lung disease 3 . (nature.com)
  • Dr. Garcia-Arcos leads a team of scientists focused on lipid metabolism, surfactant lipid homeostasis, and cellular lipid uptake and usage during pulmonary and cardiovascular disease. (downstate.edu)
  • While it has been known for decades that an adequate development of the alveolar surfactant system is essential for neonates, the role of lipid metabolism in adult lung disease is poorly understood despite accumulating evidence showing its relevance. (downstate.edu)
  • Pulmonary metabolism in smoke-related disease. (downstate.edu)
  • Surfactant protein B (SFTPB) deficiency is a fatal disease affecting newborn infants. (nature.com)
  • After differentiating the mutant and corrected cells into lung organoids, we show expression of SFTPB mRNA during endodermal and organoid differentiation but the protein product only after organoid differentiation. (nature.com)
  • Surfactant dysfunction is caused by mutations in one of several genes, including SFTPB , SFTPC , and ABCA3 . (medlineplus.gov)
  • The SFTPB and SFTPC genes provide instructions for making surfactant protein-B (SP-B) and surfactant protein-C (SP-C), respectively, two of the four proteins in surfactant. (medlineplus.gov)
  • Mutations in the SFTPB gene cause a type of surfactant dysfunction sometimes referred to as SP-B deficiency. (medlineplus.gov)
  • These mutations lead to a reduction in or absence of mature SP-B. In addition, SFTPB gene mutations cause abnormal processing of SP-C, resulting in a lack of mature SP-C and a buildup of unprocessed forms of SP-C. These changes lead to abnormal surfactant composition and decreased surfactant function. (medlineplus.gov)
  • SFTPB is the pulmonary-associated surfactant B protein (SPB), an amphipathic surfactant protein essential for lung function and homeostasis after birth. (avivasysbio.com)
  • Next are patients with genetic mutations in: surfactant protein B (SFTPB), ABCA3, surfactant protein C (SFTPC) and pulmonary alveolar proteinosis (PAP). (cincinnatichildrens.org)
  • Dipalmitoylphosphatidylcholine is a phospholipid consisting of two palmitic acids and is the major constituent of pulmonary surfactant. (absoluteastronomy.com)
  • SP-D has a significant roles in immune and inflammatory regulation of the lung as it regulates of the level of surfactant in the lungs by a process named surfactant homeostasis. (wikipedia.org)
  • In this study, we tested the possibility that CDH lungs are surfactant protein deficient, which could explain the respiratory failure and difficulties in treating CDH infants. (eur.nl)
  • Immunohistochemical analysis revealed no differences between control and CDH lungs for SP protein expression. (eur.nl)
  • Pulmonary function tests and a carbon monoxide diffusion capacity test of the lungs for carbon monoxide (DLCO) may be performed. (medscape.com)
  • Pulmonary alveolar proteinosis is a rare disorder in which the air sacs of the lungs (alveoli) become plugged with a protein- and fat-rich fluid. (msdmanuals.com)
  • The cause of pulmonary alveolar proteinosis is almost always unknown, but studies have linked it to production of an antibody directed against a protein that seems to be involved with the production or the breakdown of surfactant (a substance normally produced in the lungs). (msdmanuals.com)
  • The protein in the lungs plugs up the alveoli and small airways (bronchioles). (msdmanuals.com)
  • Dr. Ledford's current work in the area of pulmonary surfactant immunobiology combines her knowledge of mouse genetics, pulmonary disease models and immune function regulation and focuses on understanding the role of Surfactant Protein-A (SP-A) and how it regulates signaling pathways within various immune cell populations. (bio5.org)
  • Mutations in the surfactant protein C (SP-C) gene (SFTPC) are associated with familial desquamative and nonspecific interstitial pneumonitis. (nih.gov)
  • Mutations in the SFTPC gene are involved in a type of surfactant dysfunction sometimes called SP-C dysfunction. (medlineplus.gov)
  • Neonates with congenital diaphragmatic hernia (CDH) suffer from a diaphragmatic defect, lung hypoplasia, and pulmonary hypertension, with poor lung function forming the major clinical challenge. (eur.nl)
  • Dr. Pryhuber's particular clinical interests are care of infants with pulmonary hypertension, lung injury, growth and developmental failure, often complicated by chronic and inflammatory disease. (rochester.edu)
  • She leads the neonatal pulmonary hypertension consultation team. (rochester.edu)
  • Persistent pulmonary hypertension of the newborn (PPHN) is defined as the failure of the normal circulatory transition that occurs after birth. (medscape.com)
  • It is a syndrome characterized by marked pulmonary hypertension that causes hypoxemia secondary to right-to-left shunting of blood at the foramen ovale and ductus arteriosus. (medscape.com)
  • In contrast to adult primary pulmonary hypertension, the newborn syndrome is not defined by a specific pressure of the pulmonary circulation. (medscape.com)
  • Patients with DLCO of less than 60% predicted and oxygen desaturation of less than 90% on the 6-minute walk test have a high likelihood of pulmonary hypertension and should undergo further evaluation for the presence of this disorder. (medscape.com)
  • [ 51 ] In one study, patients with a saturation of less than 90% during a 6-minute walk test were 12 times more likely to have pulmonary hypertension. (medscape.com)
  • To determine the correlation between maternal bile acid (BA) level and fetal pulmonary surfactant in rats and study the effects of BA on fetal lung in rat model of intrahepatic cholestasis of pregnancy. (hindawi.com)
  • Deletion of the glucocorticoid receptor gene (Nr3c1) from fetal pulmonary mesenchymal cells phenocopied defects caused by global Nr3c1 deletion, while lung epithelial- or endothelial-specific Nr3c1 deletion did not impair lung function at birth. (stanford.edu)
  • Mar. 10, 2023 One in 10 adults suffer from the debilitating effects of chronic obstructive pulmonary disease (COPD). (sciencedaily.com)
  • Surfactant is produced by alveolar type II cells which can be differentiated in vitro from patient specific induced pluripotent stem cell (iPSC)-derived lung organoids. (nature.com)
  • In the lab, we use cell culture and in vivo models to study the regulation of surfactant homeostasis and its dysregulation during disease. (downstate.edu)
  • Congenital PAP is caused by mutations in genes required for normal surfactant production. (medscape.com)
  • These results add to the growing evidence that specific Ca2+-protein-lipid interactions are important in determining both the structure and function of extracellular lung surfactant fractions. (nih.gov)
  • The authors conclude that colchicine may have a potential role in lung injury that is associated with increased permeability or extracellular surfactant. (cdc.gov)
  • We conclude that there is no primary deficiency of surfactant proteins in the nitrofen-induced CDH rat model. (eur.nl)
  • One type of surfactant dysfunction, SP-B deficiency, is estimated to occur in 1 in 1 million newborns worldwide. (medlineplus.gov)
  • For this reason, the skin is often exposed to potentially hazardous agents, including chemicals, which may contribute to the onset of a spectrum of adverse health effects ranging from localized damage (e.g., irritant contact dermatitis and corrosion) to induction of immune-mediated responses (e.g., allergic contact dermatitis and pulmonary responses), or systemic toxicity (e.g., neurotoxicity and hepatoxicity). (cdc.gov)
  • Secondary PAP occurs in a heterogeneous group of conditions that reduce numbers or functions of alveolar macrophages and thereby surfactant clearance. (medscape.com)
  • Aim of the present study was to investigate if the pre-coating of MWCNTs with pulmonary surfactant has an influence on potential adverse effects, upon both (i) human monocyte derived macrophages (MDM) monocultures, and (ii) a sophisticated in vitro model of the human epithelial airway barrier. (biomedcentral.com)
  • The exaggerated immune response to repeated inhalation of these particles leads to infiltration and proliferation of activated pulmonary macrophages and lymphocytes, resulting in lymphocytic alveolitis and bronchiolitis with noncaseating granulomas. (cdc.gov)
  • Each of these genes is involved in the production of surfactant. (medlineplus.gov)
  • Chloroquine has also been shown to be efficacious for the treatment and maintenance of chronic pulmonary sarcoidosis. (medscape.com)
  • Surfactant protein A contains a N-terminal collagen-like domain and a C-terminal lectin domain that are characteristic of members of the collectin family of proteins. (nih.gov)
  • Recently, the abnormalities of pulmonary surfactant system have been implicated in the pathogenesis of respiratory distress syndrome [ 6 , 7 ]. (hindawi.com)
  • Blood test results may show abnormalities that occur in pulmonary alveolar proteinosis as well as in other disorders. (msdmanuals.com)
  • She serves on NIH study sections and as reviewer for journals in her area of expertise, manages an active laboratory, supervises students in pulmonary biology and epithelial cell research and has received awards recognizing both teaching and original research accomplishments. (rochester.edu)
  • The distal lung is a honeycomb-like collection of delicate gas exchange sacs called alveoli lined by two interspersed epithelial cell types: the cuboidal, surfactant-producing alveolar type II (AT2) and the flat, gas-exchanging alveolar type I (AT1) cell. (stanford.edu)
  • Surfactant is released from the lung cells and spreads across the tissue that surrounds alveoli. (medlineplus.gov)
  • Found in the lung parenchyma, the pulmonary alveoli are the dead ends of the respiratory tree, which outcrop from either alveolar sacs or alveolar ducts, which are both sites of gas exchange with the blood as well. (absoluteastronomy.com)
  • It is a condition where the alveoli are deflated, as distinct from pulmonary consolidation.It is a very common finding in chest x-rays and other. (absoluteastronomy.com)
  • In the alveoli, MWCNTs first interact with the pulmonary surfactant. (biomedcentral.com)
  • To make a definitive diagnosis of pulmonary alveolar proteinosis, doctors examine a sample of the fluid from the alveoli. (msdmanuals.com)
  • For example, levels of some substances (for example, lactic dehydrogenase, red blood cells, serum surfactant proteins, and gamma globulin) are often elevated. (msdmanuals.com)
  • Researchers in Finland are reporting identification of the first potential "biomarker" that could be used in development of a sputum test for early detection of chronic obstructive pulmonary disease (COPD). (sciencedaily.com)
  • Background: Welders are exposed to gas and particle emissions that can cause severe lung disease, such as chronic obstructive pulmonary disease (COPD), a leading cause of mortality and morbidity worldwide. (lu.se)
  • SP-A is a major player in the pulmonary cytokine-network and moreover has been described to act in the pulmonary host defense. (iospress.com)
  • The diagnosis is confirmed regardless of the pulmonary arterial pressure, as long as it is accompanied by a right-to-left shunt and absence of congenital heart disease. (medscape.com)
  • We investigated this hypothesis in the nitrofen-induced CDH rat model and assessed the cellular concentrations of surfactant protein (SP)-A, -B, and -C mRNA with a quantitative radioactive in situ hybridization technique. (eur.nl)
  • These misfolded proteins may trigger a cellular response that results in cell damage and death. (medlineplus.gov)
  • SP-A-deficient mice have an enhanced susceptibility to infection to pulmonary infection with bacterial and fungal pathogens and collectin replacement in these animals corrects defects in dysregulated cellular functions and microbial clearance. (fz-borstel.de)
  • Previous reports demonstrate that surfactant protein-A (SP-A) binds live M. pneumoniae and mycoplasma membrane fractions (MMF) with high affinity. (bio5.org)
  • An abundant pulmonary surfactant-associated protein that binds to a variety of lung pathogens, resulting in their opsinization. (nih.gov)
  • Recently, bile acid was found to cause surfactant inactivation by enhancing the activity of secretory phospholipase A2 (sPLA2) and induce inflammatory response of fetal lung [ 5 , 8 ]. (hindawi.com)
  • Deficiencies and inactivation of surfactant have been associated with a variety of human lung diseases in both infants and adults. (fz-borstel.de)
  • We believe the answer is probable, since some of the systemic disease clinical manifestations of COVID-19 cannot be explained solely by the binding of SARS-CoV-2 spike proteins with cell membranes of tissues that exhibit angiotensin-converting enzyme 2 (ACE2). (frontiersin.org)
  • Hypersensitivity pneumonitis, also known as extrinsic allergic alveolitis, is an uncommon non-immunoglobulin E (IgE), T-helper cell type 1 (Th1)-mediated inflam- matory pulmonary disease with systemic symptoms resulting from repeated inhalation and subsequent sensitization to a large variety of aerosolized antigenic organic dust particles. (cdc.gov)
  • We sought to determine whether immune reactivity occurs between anti-SARS-CoV-2 protein antibodies and human tissue antigens, and whether molecular mimicry between COVID-19 viral proteins and human tissues could be the cause. (frontiersin.org)
  • We applied both human monoclonal anti-SARS-Cov-2 antibodies (spike protein, nucleoprotein) and rabbit polyclonal anti-SARS-Cov-2 antibodies (envelope protein, membrane protein) to 55 different tissue antigens. (frontiersin.org)
  • We found that SARS-CoV-2 antibodies had reactions with 28 out of 55 tissue antigens, representing a diversity of tissue groups that included barrier proteins, gastrointestinal, thyroid and neural tissues, and more. (frontiersin.org)
  • In this mechanism, antibodies formed against SARS-CoV-2 would also bind to human tissue proteins leading to autoimmune reactivity. (frontiersin.org)
  • Tests for granulocyte macrophage colony stimulating factor (GM-CSF) antibodies can also be performed to help support the diagnosis of an autoimmune form of pulmonary alveolar proteinosis. (msdmanuals.com)
  • However, whether the level of TBA in maternal serum caused perinatal abnormality of pulmonary surfactant and fetal lung tissue morphological structure remains largely unknown. (hindawi.com)
  • We also did selective epitope mapping using BLAST and showed similarities and homology between spike, nucleoprotein, and many other SARS-CoV-2 proteins with the human tissue antigens mitochondria M2, F-actin and TPO. (frontiersin.org)
  • Cross-reactivity occurs when amino acid sequence homology exists between a pathogen and self-tissue proteins ( 1 ). (frontiersin.org)
  • LOXL2 protein expression is observed in the fibroblastic foci and collagenous regions of diseased IPF lung tissue, with relatively minor expression in healthy lung tissue [ 9 ]. (ersjournals.com)
  • Description: This is Double-antibody Sandwich Enzyme-linked immunosorbent assay for detection of Rat Surfactant Associated Protein C (SPC) in Tissue homogenates, cell lysates, lung lavage fluid and other biological fluids. (stemcellcharter.org)
  • Description: A sandwich quantitative ELISA assay kit for detection of Human Surfactant Associated Protein C (SPC) in samples from serum, plasma, tissue homogenates, cell lysates, lung lavage fluid, cell culture supernates or other biological fluids. (stemcellcharter.org)
  • Neither artificial membrane slabs, nor 'live cells' imaged under conditions in which cells have a shabby life that doesn't last long (how much of this is due to the mistreatment of the membrane proteins? (biophysics.org)
  • As to the role of the cytoskeleton, what does this tell us about the membrane itself, or the behavior of membrane proteins as individual molecules in their interplay with the membrane? (biophysics.org)
  • Lack of mature SP-C can lead to abnormal composition of surfactant and decreased surfactant function. (medlineplus.gov)
  • Air trapping is a common feature in sarcoidosis that can be supported with imaging studies and correlates with evidence of small airways disease on pulmonary function testing. (medscape.com)
  • By the use of cell culture … or animal models the functional properties have been repeatedly shown in many aspects often bearing surprising properties which strongly indicate the physiological importance of SP-A. To date SP-A is recognized as a molecule essential for pulmonary development, structure and function. (iospress.com)
  • However, data suggest early treatment of stage II sarcoidosis with oral prednisolone for 3 months followed by inhaled budesonide for 15 months improves 5-year pulmonary function and reduces the need for future steroid treatment. (medscape.com)
  • This article gives an overview about the state of knowledge on SP-A focussed in applications for human pulmonary disorders and points out the importance for pathology-orientated research approaches using immunohistochemistry or in Situ hybridization as promising methods to further elucidate the role of this molecule in adult lung diseases. (iospress.com)
  • Less severe forms of surfactant dysfunction cause gradual onset of breathing problems in children or adults. (medlineplus.gov)
  • Intratracheally injection of bile acid had been shown to induce severe pulmonary edema in rabbits [ 15 ]. (hindawi.com)
  • An upcoming number of reports deals with the role of SP-A for pulmonary pathology. (iospress.com)
  • In molecular biology, Pulmonary surfactant protein D (SP-D) is a protein domain predominantly found in lung surfactant. (wikipedia.org)
  • These antigens include organic dusts containing bacteria, fungi,4 animal or plant proteins, or low-molecular-weight chemicals. (cdc.gov)
  • Lung measurements were performed with standard spirometry and new methods: airspace dimension assessment (AiDA), oscillometry, blood serum biomarkers (club cell secretory protein 16, surfactant protein D, matrix metalloproteinases, fibroblast, hepatocyte growth factor, interleukins), and one urine biomarker (desmosine). (lu.se)
  • Finally, the further GIX sPLA 2 s are found in venom of marine snails, and GXIA and GXIB sPLA 2 s are plant proteins. (ijbs.com)
  • In one study, treatment of acute exacerbations of pulmonary sarcoidosis with steroid doses as low as 20 mg of prednisone for a median of 21 days improved spirometry back to baseline and improved clinical symptoms. (medscape.com)