Chemokines
Chemokines, CXC
Chemokines, CC
Receptors, Chemokine
Chemokine CCL5
Chemokine CXCL10
Chemokines, C
Chemokine CCL2
Chemokine CCL4
Chemokine CCL3
Macrophage Inflammatory Proteins
Chemokine CXCL1
Chemokines, CX3C
Chemokine CCL7
Cytokines
Chemokine CXCL11
Monocyte Chemoattractant Proteins
Chemotaxis, Leukocyte
Chemokine CXCL2
Receptors, Interleukin-8B
Chemokine CXCL5
Interleukin-8
Receptors, CXCR3
Duffy Blood-Group System
Receptors, CCR2
Chemokine CCL17
Receptors, CCR1
Chemokine CCL19
Chemotactic Factors
Chemokine CCL21
Chemokine CCL8
Chemokine CCL11
Chemotaxis
Chemokine CCL22
Monokines
Chemokine CXCL12
Inflammation
Chemokine CCL1
Receptors, CCR5
Receptors, Interleukin-8A
Cells, Cultured
Receptors, CCR3
Mice, Inbred C57BL
Chemokine CCL24
Cell Movement
Chemokine CXCL6
RNA, Messenger
Chemokine CX3CL1
Receptors, CCR10
Inflammation Mediators
Receptors, CXCR4
Neutrophil Infiltration
Receptors, Cytokine
Chemokine CXCL13
Neutrophils
Monocytes
Intercellular Signaling Peptides and Proteins
Leukocytes
Chemokine CCL20
Receptors, CCR4
Macrophages
Mice, Knockout
Signal Transduction
Receptors, CCR7
Gene Expression Regulation
Mice, Inbred BALB C
T-Lymphocytes
Lung
Receptors, CCR8
Tumor Necrosis Factor-alpha
beta-Thromboglobulin
Up-Regulation
Reverse Transcriptase Polymerase Chain Reaction
Interferon-gamma
Dendritic Cells
Enzyme-Linked Immunosorbent Assay
Disease Models, Animal
Immunity, Innate
NF-kappa B
Chemotactic Factors, Eosinophil
Lipopolysaccharides
Flow Cytometry
Eosinophils
Th2 Cells
Platelet Factor 4
Receptors, CCR6
Gene Expression
Ligands
Th1 Cells
Epithelial Cells
Bronchoalveolar Lavage Fluid
Leukocytes, Mononuclear
Receptors, CXCR5
Gene Expression Profiling
Molecular Sequence Data
Cell Migration Inhibition
Chemokine CCL27
Growth Substances
Immunohistochemistry
Neutrophil Activation
Intercellular Adhesion Molecule-1
Amino Acid Sequence
Interleukin-6
Oligonucleotide Array Sequence Analysis
Endothelial Cells
CD4-Positive T-Lymphocytes
Cell Adhesion Molecules
Receptors, Interleukin
Lymphocyte Activation
Interleukin-1beta
Receptors, Cell Surface
Toll-Like Receptors
Mice, Transgenic
Interleukin-1
Lymphocytes
Endothelium, Vascular
Skin
Biological Markers
Protein Binding
Cell Communication
Antigens, CD
Microglia
Interleukins
Leukocyte Rolling
Vascular Cell Adhesion Molecule-1
Down-Regulation
Case-Control Studies
Culture Media, Conditioned
Lymphoid Tissue
Macrophages, Alveolar
Lymph Nodes
Coculture Techniques
HIV-1
CD8-Positive T-Lymphocytes
Cell Differentiation
Models, Immunological
Receptors, HIV
Respiratory Mucosa
Fibroblasts
Uteroglobin
Stromal Cells
Interleukin-17
Angiostatic Proteins
Neovascularization, Pathologic
Macrophage Activation
Toll-Like Receptor 4
Genotype
Lymphotoxin-beta
Real-Time Polymerase Chain Reaction
Receptors, Interleukin-17
Arthritis, Rheumatoid
Integrin alpha4beta1
Disease Progression
Synovial Membrane
T-Lymphocyte Subsets
Base Sequence
Interleukin-10
Endothelium, Lymphatic
Toll-Like Receptor 2
Mast Cells
Glycosaminoglycans
Asthma
Killer Cells, Natural
Allergens
Interleukin-4
Polymorphism, Genetic
Astrocytes
Polymerase Chain Reaction
Interleukin-13
Dose-Response Relationship, Drug
Virus Replication
Antigens, CD11b
Interleukin-1alpha
Calcium
Toll-Like Receptor 3
Blotting, Western
Hypersensitivity
Expression and cellular localization of the CC chemokines PARC and ELC in human atherosclerotic plaques. (1/1708)
Local immune responses are thought to play an important role in the development of atherosclerosis. Histological studies have shown that human atherosclerotic lesions contain T lymphocytes throughout all stages of development, many of which are in an activated state. A number of novel CC chemokines have been described recently, which are potent chemoattractants for lymphocytes: PARC (pulmonary and activation-regulated chemokine), ELC (EBI1-ligand chemokine), LARC (liver and activation-regulated chemokine), and SLC (secondary lymphoid-tissue chemokine). Using reverse transcriptase-polymerase chain reaction and in situ hybridization, we have found gene expression for PARC and ELC but not for LARC or SLC in human atherosclerotic plaques. Immunohistochemical staining of serial plaque sections with specific cell markers revealed highly different expression patterns of PARC and ELC. PARC mRNA was restricted to CD68+ macrophages (n = 14 of 18), whereas ELC mRNA was widely expressed by macrophages and intimal smooth muscle cells (SMC) in nearly all of the lesions examined (n = 12 of 14). ELC mRNA was also found to be expressed in the medial SMC wall of highly calcified plaques (n = 4). Very low levels of ELC mRNA expression could also be detected in normal mammary arteries but no mRNA expression for PARC was detected in these vessels (n = 4). In vitro, ELC mRNA was found to be up-regulated in aortic SMC stimulated with tumor necrosis factor-a and interferon-gamma but not in SMC stimulated with serum. Both PARC and ELC mRNA were expressed by monocyte-derived macrophages but not monocytes. The expression patterns of PARC and ELC mRNA in human atherosclerotic lesions suggest a potential role for these two recently described CC chemokines in attracting T lymphocytes into atherosclerotic lesions. (+info)Selective eosinophil transendothelial migration triggered by eotaxin via modulation of Mac-1/ICAM-1 and VLA-4/VCAM-1 interactions. (2/1708)
We have recently cloned eotaxin, a highly efficacious eosinophilic chemokine involved in the development of lung eosinophilia during allergic inflammatory reactions. To understand more precisely how eotaxin facilitates the specific migration of eosinophils, we have studied which adhesion receptors are essential for eotaxin action both in vivo and in vitro. Experiments using mice genetically deficient in adhesion receptors demonstrated that molecules previously reported to be involved in both leukocyte tethering/rolling (P-selectin and E-selectin) and in sticking/ transmigration (ICAM-1 and VCAM-1) are required for eotaxin action in vivo. To further elucidate the mechanism(s) involved in this process, we have used an in vitro transendothelial chemotaxis model. mAb neutralization studies performed in this system suggest that the integrins Mac-1 (CD11b/18), VLA-4 (alpha4beta1) and LFA-1 (CD11a/18) are involved in the transendothelial chemotaxis of eosinophils to eotaxin. Accordingly, the expression of these integrins on eosinophils is elevated by direct action of this chemokine in a concentration-dependent manner. Taken together, our results suggest that eotaxin-induced eosinophil transendothelial migration in vivo and in vitro relies on Mac-1/ICAM-1 and VLA-4NCAM-1 interactions, the latter ones becoming more relevant at later time points of the eotaxin-induced recruitment process. (+info)Selective recruitment of CCR4-bearing Th2 cells toward antigen-presenting cells by the CC chemokines thymus and activation-regulated chemokine and macrophage-derived chemokine. (3/1708)
Helper T cells are classified into Th1 and Th2 subsets based on their profiles of cytokine production. Th1 cells are involved in cell-mediated immunity, whereas Th2 cells induce humoral responses. Selective recruitment of these two subsets depends on specific adhesion molecules and specific chemoattractants. Here, we demonstrate that the T cell-directed CC chemokine thymus and activation-regulated chemokine (TARC) was abundantly produced by monocytes treated with granulocyte macrophage colony stimulating factor (GM-CSF) or IL-3, especially in the presence of IL-4 and by dendritic cells derived from monocytes cultured with GM-CSF + IL-4. The receptor for TARC and another macrophage/dendritic cell-derived CC chemokine macrophage-derived chemokine (MDC) is CCR4, a G protein-coupled receptor. CCR4 was found to be expressed on approximately 20% of adult peripheral blood effector/memory CD4+ T cells. T cells attracted by TARC and MDC generated cell lines predominantly producing Th2-type cytokines, IL-4 and IL-5. Fractionated CCR4+ cells but not CCR4- cells also selectively gave rise to Th2-type cell lines. When naive CD4+ T cells from adult peripheral blood were polarized in vitro, Th2-type cells selectively expressed CCR4 and vigorously migrated toward TARC and MDC. Taken together, CCR4 is selectively expressed on Th2-type T cells and antigen-presenting cells may recruit Th2 cells expressing CCR4 by producing TARC and MDC in Th2-dominant conditions. (+info)Eotaxin contributes to renal interstitial eosinophilia. (4/1708)
BACKGROUND: A potent eosinophil chemotactic cytokine, human eotaxin, is directly chemotactic for eosinophils. Therefore, the specific expression of eotaxin in tissue might play a crucial role in tissue eosinophilia. However, the precise molecular mechanism of the recruitment and activation of eosinophils in human renal diseases remains to be investigated. We evaluated the role of eotaxin in the pathogenesis of human diffuse interstitial nephritis with marked infiltration of eosinophils. METHODS: In this study, we examined 20 healthy volunteers. 56 patients with primary or secondary glomerular diseases and two hypereosinophilic syndrome patients without renal involvement. Urinary and serum eotaxin levels were determined by an enzyme-linked immunosorbent assay. We also detected the presence of eotaxin protein immunohistochemically. RESULTS: On the one hand, urinary levels of eotaxin were significantly higher before the initiation of glucocorticoid administration in the patient with interstitial nephritis with marked infiltration of eosinophils. On the other hand, urinary eotaxin levels were not detected in any patients with nephrotic syndrome, interstitial nephritis without eosinophils, hypereosinophilic syndrome without renal involvement or other renal diseases. Serum eotaxin levels were not detected in any of the patients. Therefore, the detection of eotaxin in the urine was specific for renal interstitial eosinophilia. Moreover, endothelial cells, infiltrating mononuclear cells and renal epithelial cells in the tubulointerstitial lesions were immunostained with specific anti-eotaxin antibodies. Furthermore, the elevated urinary levels of eotaxin decreased dramatically during glucocorticoid-induced convalescence. HYPOTHESIS: We hypothesize that in situ expression of eotaxin may provide a new mechanism to explain the renal interstitial eosinophil infiltration. (+info)Induction of macrophage C-C chemokine expression by titanium alloy and bone cement particles. (5/1708)
Particulate wear debris is associated with periprosthetic inflammation and loosening in total joint arthroplasty. We tested the effects of titanium alloy (Ti-alloy) and PMMA particles on monocyte/macrophage expression of the C-C chemokines, monocyte chemoattractant protein-1 (MCP-1), monocyte inflammatory protein-1 alpha (MIP-1alpha), and regulated upon activation normal T expressed and secreted protein (RANTES). Periprosthetic granulomatous tissue was analysed for expression of macrophage chemokines by immunohistochemistry. Chemokine expression in human monocytes/macrophages exposed to Ti-alloy and PMMA particles in vitro was determined by RT-PCR, ELISA and monocyte migration. We observed MCP-1 and MIP-1alpha expression in all tissue samples from failed arthroplasties. Ti-alloy and PMMA particles increased expression of MCP-1 and MIP-1alpha in macrophages in vitro in a dose- and time-dependent manner whereas RANTES was not detected. mRNA signal levels for MCP-1 and MIP-1alpha were also observed in cells after exposure to particles. Monocyte migration was stimulated by culture medium collected from macrophages exposed to Ti-alloy and PMMA particles. Antibodies to MCP-1 and MIP-1alpha inhibited chemotactic activity of the culture medium samples. Release of C-C chemokines by macrophages in response to wear particles may contribute to chronic inflammation at the bone-implant interface in total joint arthroplasty. (+info)Presence of P210bcrabl is associated with decreased expression of a beta chemokine C10 gene in a P210bcrabl-positive myeloid leukemia cell line. (6/1708)
BACKGROUND: Chronic myelogenous leukemia (CML) is thought to start with the acquisition of the t(9;22) chromosomal translocation that codes for the P210bcrabl tyrosine-specific protein kinase. The CML cells exhibit anchorage-independent cell growth and genetic instability. After the initial phase, the cells acquire the phenotype of growth factor-independent growth. After the chronic phase, the disease evolves into the accelerated and blastic phases through the process of sequential random mutation. MATERIALS AND METHODS: To identify some of the genetic changes that contribute to the phenotype of blastic and accelerated phase cells, we used differential display PCR to compare levels of cDNA reverse transcripts of mRNA in 32Dc13 cells and 32Dc13 cells that were stably transfected with a bcrabl cDNA plasmid in a constitutively expressed transcription unit. These cells were designated 32Dc13P210bcrabl. For these studies, we used the 32D myeloid leukemia cell line, which depends on IL-3 for growth. RESULTS: Following introduction of the bcr-abl cDNA through transfection, the cell line became growth factor independent, mimicking the change in phenotype that occurs during the later phases of CML. These differential display screening assays detected altered levels of transcripts for 28 genes. Of interest to the biology of growth factor-independent growth in the bcrabl-positive 32D cells was the fact that the C10 beta chemokine gene was expressed at higher levels in the 32Dc13 cells than in the 32Dc13P210bcrabl cells. CONCLUSIONS: These studies show that a C10 beta chemokine gene was expressed at different levels with or without P210bcrabl. (+info)Cutting edge: secondary lymphoid-tissue chemokine (SLC) and CC chemokine receptor 7 (CCR7) participate in the emigration pathway of mature dendritic cells from the skin to regional lymph nodes. (7/1708)
Dendritic cells (DCs) emigrate to regional lymph nodes (LNs) during immune responses via afferent lymphatic channels. Secondary lymphoid-tissue chemokine (SLC), a CC chemokine, is expressed in secondary lymphoid organs and mediates the chemotaxis of lymphocytes and DCs via its receptor, CC chemokine receptor 7 (CCR7). By dual-label fluorescence confocal microscopy, we showed MHC class II-positive cells within SLC-staining lymphatic channels in the mouse dermis. SLC was a potent in vitro chemoattractant for cultured, migratory skin DCs, and it enhanced the emigration of MHC class II-positive DCs from mouse skin explants by an average of 2.5-fold. Mature or cytokine-activated, but not resting, Langerhans cells expressed CCR7 mRNA by RT-PCR. Anti-SLC Abs, but not control or anti-eotaxin Abs, blocked the in vivo migration of 51Cr-labeled, skin-derived DCs from footpads to draining LNs by 50% (n = 9, p < 0. 005). Thus, we provide direct evidence that SLC and CCR7 participate in the emigration of DCs from peripheral tissue to LNs via lymphatics. (+info)Effects of Th2 cytokines on chemokine expression in the lung: IL-13 potently induces eotaxin expression by airway epithelial cells. (8/1708)
Airway inflammation associated with asthma is characterized by massive infiltration of eosinophils, mediated in part by specific chemoattractant factors produced in the lung. Allergen-specific Th2 cells appear to play a central role in asthma; for example, adoptively transferred Th2 cells induced lung eosinophilia associated with induction of specific chemokines. Interestingly, Th2 supernatant alone administered intranasally to naive mice induced eotaxin, RANTES, monocyte-chemotactic protein-1, and KC expression along with lung eosinophilia. We tested the major cytokines individually and found that IL-4 and IL-5 induced higher levels of macrophage-inflammatory protein-1alpha and KC; IL-4 also increased the production of monocyte-chemotactic protein-1; IL-13 and IL-4 induced eotaxin. IL-13 was by far the most potent inducer of eotaxin; indeed, a neutralizing anti-IL-13 Ab removed most of the eotaxin-inducing activity from Th2 supernatants, although it did not entirely block the recruitment of eosinophils. While TNF-alpha did not stimulate eotaxin production by itself, it markedly augmented eotaxin induction by IL-13. IL-13 was able to induce eotaxin in the lung of JAK3-deficient mice, suggesting that JAK3 is not required for IL-13 signaling in airway epithelial cells; however, eosinophilia was not induced in this situation, suggesting that JAK3 transduces other IL-13-mediated mechanisms critical for eosinophil recruitment. Our study suggests that IL-13 is an important mediator in the pathogenesis of asthma and therefore a potential target for asthma therapy. (+info)Chemokines are a family of small signaling proteins that play a crucial role in the immune system. They are produced by various cells in response to infection, injury, or inflammation and act as chemical messengers to attract immune cells to the site of injury or infection. Chemokines bind to specific receptors on the surface of immune cells, such as neutrophils, monocytes, and lymphocytes, and guide them to the site of infection or injury. They also play a role in regulating the migration and activation of immune cells within tissues. In the medical field, chemokines are important for understanding and treating various diseases, including cancer, autoimmune disorders, and infectious diseases. They are also being studied as potential therapeutic targets for the development of new drugs to treat these conditions.
Chemokines, CXC are a family of small proteins that play a crucial role in the immune system. They are secreted by various cells in response to infection, injury, or inflammation and act as chemoattractants to recruit immune cells to the site of injury or infection. CXC chemokines are characterized by the presence of a conserved cysteine (C) at the first position and a glutamine (Q) or glutamic acid (E) at the second position in their amino acid sequence. They are classified into four subfamilies based on the position of the second cysteine residue: CX3C, CXCL, CXCL1, and CXCL2. CXC chemokines play a critical role in the recruitment and activation of immune cells, including neutrophils, monocytes, and lymphocytes, to the site of infection or injury. They also play a role in the development of chronic inflammatory diseases, such as asthma, rheumatoid arthritis, and atherosclerosis. In the medical field, CXC chemokines are used as diagnostic markers for various diseases, including cancer, infectious diseases, and autoimmune disorders. They are also being investigated as potential therapeutic targets for the treatment of these diseases.
Chemokines, CC are a family of small proteins that play a crucial role in the immune system by regulating the movement of immune cells, such as white blood cells, to specific areas of the body in response to infection or injury. They are classified based on the number of cysteine residues in their amino acid sequence, with CC chemokines having two cysteines at the amino terminus. CC chemokines are involved in the recruitment of immune cells to sites of inflammation and are also involved in the development of certain types of cancer.
Receptors, Chemokine are proteins found on the surface of cells that bind to specific chemokines, which are small signaling molecules that play a role in immune cell trafficking and inflammation. These receptors are involved in the regulation of immune cell migration and are important for the recruitment of immune cells to sites of infection or injury. There are several different types of chemokine receptors, each of which is specific to a particular chemokine or group of chemokines. Dysregulation of chemokine receptors has been implicated in a variety of diseases, including cancer, autoimmune disorders, and infectious diseases.
Chemokine CCL5, also known as RANTES (regulated on activation, normal T cell expressed and secreted), is a small protein that plays a role in the immune system. It is a type of chemokine, which are signaling molecules that help to direct the movement of immune cells to specific areas of the body in response to infection or injury. CCL5 is produced by a variety of cells, including immune cells such as T cells, macrophages, and dendritic cells, as well as non-immune cells such as endothelial cells and fibroblasts. It acts on specific receptors on the surface of immune cells to attract them to the site of infection or injury. CCL5 has been implicated in a number of different diseases and conditions, including asthma, chronic obstructive pulmonary disease (COPD), and certain types of cancer. It is also involved in the recruitment of immune cells to sites of inflammation, and has been shown to play a role in the development of autoimmune diseases such as rheumatoid arthritis. Overall, CCL5 is an important molecule in the immune system that helps to regulate the movement of immune cells and plays a role in the body's response to infection and injury.
Chemokine CXCL10, also known as interferon-gamma-inducible protein 10 (IP-10), is a small protein that plays a role in the immune system. It is produced by various cells in response to infection, inflammation, or other stimuli, and it functions as a chemoattractant, recruiting immune cells to the site of infection or injury. CXCL10 is a member of the CXC chemokine family, which is a group of proteins that are involved in the recruitment and activation of immune cells. It is particularly important in the immune response to viral infections, as it helps to recruit and activate T cells and natural killer (NK) cells, which are important for controlling viral infections. In addition to its role in the immune response, CXCL10 has been implicated in a number of other physiological processes, including angiogenesis (the formation of new blood vessels), tissue repair, and the regulation of inflammation. It has also been studied in the context of various diseases, including cancer, autoimmune disorders, and infectious diseases.
Chemokines, C are a family of small signaling proteins that play a crucial role in the immune system. They are responsible for attracting immune cells to specific areas of the body where they are needed to fight infections or inflammation. The C chemokines are a subfamily of chemokines that are characterized by a conserved cysteine residue at the amino terminus of the protein. They are involved in the recruitment of monocytes, dendritic cells, and T cells to sites of inflammation or infection. Some examples of C chemokines include CCL2 (also known as MCP-1), CCL3 (also known as MIP-1α), and CCL4 (also known as MIP-1β). These chemokines are produced by a variety of cells, including macrophages, endothelial cells, and fibroblasts, in response to inflammatory stimuli such as cytokines or bacterial or viral infections. Abnormal regulation of C chemokines has been implicated in a number of diseases, including atherosclerosis, asthma, and certain types of cancer. Therefore, understanding the role of C chemokines in the immune system is important for developing new therapies for these diseases.
Chemokine CXCL9, also known as interferon-inducible protein 10 (IP-10), is a small protein that plays a role in the immune response. It is a type of chemokine, which are proteins that help to direct the movement of immune cells to specific areas of the body where they are needed. CXCL9 is produced by a variety of cells, including immune cells such as T cells and macrophages, in response to the presence of certain stimuli, such as viral infections or inflammatory signals. It functions by binding to specific receptors on the surface of immune cells, which triggers a signaling cascade that leads to the activation and recruitment of these cells to the site of inflammation. In the context of medical research, CXCL9 has been studied for its potential role in a variety of conditions, including viral infections, autoimmune diseases, and cancer. For example, high levels of CXCL9 have been associated with the progression of certain types of cancer, and it has been proposed as a potential target for the development of new cancer therapies.
Chemokine CCL2, also known as monocyte chemoattractant protein-1 (MCP-1), is a small protein that plays a crucial role in the immune system. It is a member of the chemokine family of proteins, which are responsible for regulating the movement of immune cells within the body. CCL2 is primarily produced by cells such as monocytes, macrophages, and endothelial cells in response to inflammatory stimuli. It functions as a chemoattractant, drawing immune cells towards the site of inflammation or infection. Specifically, CCL2 attracts monocytes and T cells to the site of injury or infection, where they can help to clear the infection and promote tissue repair. In addition to its role in immune cell recruitment, CCL2 has also been implicated in a variety of other physiological processes, including angiogenesis (the formation of new blood vessels), tissue repair, and cancer progression. Dysregulation of CCL2 expression or function has been linked to a number of diseases, including atherosclerosis, diabetes, and certain types of cancer.
Chemokine CCL4, also known as macrophage inflammatory protein 1β (MIP-1β), is a small protein that plays a role in the immune system. It is a type of chemokine, which are a group of signaling molecules that help to direct the movement of immune cells to specific areas of the body in response to infection or injury. CCL4 is produced by a variety of cells, including macrophages, monocytes, and T cells. It is involved in the recruitment of immune cells to sites of inflammation and is also thought to play a role in the development of certain types of cancer. In the medical field, CCL4 is often studied as a potential target for the treatment of diseases such as cancer, autoimmune disorders, and viral infections. It is also used as a diagnostic marker for certain conditions, such as HIV infection and liver disease.
Chemokine CCL3, also known as macrophage inflammatory protein 1α (MIP-1α), is a type of chemokine protein that plays a role in the immune system. It is produced by various cells, including macrophages, monocytes, and dendritic cells, in response to infection or inflammation. CCL3 functions as a chemoattractant, drawing immune cells to the site of infection or injury. It also has other functions, such as promoting the activation and differentiation of immune cells, and regulating the inflammatory response. In the medical field, CCL3 is often studied in the context of various diseases, including HIV/AIDS, cancer, and autoimmune disorders. For example, high levels of CCL3 have been associated with poor outcomes in HIV/AIDS, and it has been proposed as a potential therapeutic target for the disease. Additionally, CCL3 has been implicated in the development and progression of certain types of cancer, such as breast cancer and lung cancer.
Macrophage Inflammatory Proteins (MIPs) are a family of small proteins that are produced by macrophages, a type of white blood cell. These proteins play a role in the immune response by promoting inflammation and attracting other immune cells to the site of infection or injury. MIPs are also involved in the regulation of angiogenesis, the formation of new blood vessels, and in the development of certain types of cancer. There are several different types of MIPs, including MIP-1α, MIP-1β, and MIP-2, each with its own specific functions and effects on the immune system.
Chemokine CXCL1, also known as Interleukin-8 (IL-8), is a type of protein that plays a crucial role in the immune system. It is a chemokine, which means that it is a type of signaling molecule that attracts immune cells to specific areas of the body in response to infection or injury. CXCL1 is produced by a variety of cells, including immune cells such as neutrophils, monocytes, and macrophages, as well as epithelial cells and fibroblasts. It is primarily involved in the recruitment of neutrophils to sites of inflammation, where they help to fight off infection and clear damaged tissue. In addition to its role in inflammation, CXCL1 has been implicated in a number of other biological processes, including cancer progression, angiogenesis (the formation of new blood vessels), and tissue repair. It is also a potential therapeutic target for the treatment of a variety of diseases, including cancer, autoimmune disorders, and inflammatory conditions.
Chemokines, CX3C are a family of small proteins that play a crucial role in the immune system. They are chemotactic cytokines, meaning they attract immune cells to specific areas of the body in response to infection or injury. The CX3C chemokines are a subfamily of chemokines that are characterized by a conserved cysteine residue at the N-terminus and a cysteine residue at the C-terminus that forms a disulfide bond. The most well-known member of this subfamily is fractalkine (CX3CL1), which is expressed on the surface of endothelial cells, neurons, and other cell types. Fractalkine acts as a chemoattractant for immune cells, including monocytes, dendritic cells, and T cells, and plays a role in the recruitment of these cells to sites of inflammation. It also has anti-inflammatory properties and has been implicated in the regulation of immune cell trafficking and the development of autoimmune diseases. Overall, chemokines, CX3C are important mediators of immune cell trafficking and play a critical role in the immune response to infection and injury.
Chemokine CCL7, also known as monocyte chemoattractant protein-1 (MCP-1), is a small protein that plays a role in the immune system. It is a type of chemokine, which are a group of signaling molecules that help to direct the movement of immune cells to specific areas of the body in response to infection or injury. CCL7 is produced by a variety of cells, including monocytes, macrophages, and endothelial cells, and it is involved in the recruitment of monocytes and other immune cells to sites of inflammation. It does this by binding to specific receptors on the surface of immune cells, which triggers a signaling cascade that leads to the activation and movement of these cells. In the medical field, CCL7 is often studied in the context of various diseases and conditions, including cancer, autoimmune disorders, and infectious diseases. For example, high levels of CCL7 have been associated with the development and progression of certain types of cancer, such as breast cancer and lung cancer. It is also involved in the recruitment of immune cells to sites of inflammation in autoimmune disorders, such as rheumatoid arthritis, and it plays a role in the immune response to infections, such as tuberculosis. Overall, CCL7 is an important molecule in the immune system that helps to regulate the movement of immune cells to specific areas of the body. It is involved in a variety of physiological processes and has been implicated in the development and progression of certain diseases and conditions.
Cytokines are small proteins that are produced by various cells of the immune system, including white blood cells, macrophages, and dendritic cells. They play a crucial role in regulating immune responses and inflammation, and are involved in a wide range of physiological processes, including cell growth, differentiation, and apoptosis. Cytokines can be classified into different groups based on their function, including pro-inflammatory cytokines, anti-inflammatory cytokines, and regulatory cytokines. Pro-inflammatory cytokines, such as tumor necrosis factor-alpha (TNF-alpha) and interleukin-1 (IL-1), promote inflammation and recruit immune cells to the site of infection or injury. Anti-inflammatory cytokines, such as interleukin-10 (IL-10) and transforming growth factor-beta (TGF-beta), help to dampen the immune response and prevent excessive inflammation. Regulatory cytokines, such as interleukin-4 (IL-4) and interleukin-13 (IL-13), help to regulate the balance between pro-inflammatory and anti-inflammatory responses. Cytokines play a critical role in many diseases, including autoimmune disorders, cancer, and infectious diseases. They are also important in the development of vaccines and immunotherapies.
Chemokine CXCL11, also known as interferon-inducible protein 10 (IP-10) or lymphotactin, is a small protein that plays a role in the immune system. It is a type of chemokine, which are proteins that help to direct the movement of immune cells to specific areas of the body in response to infection or injury. CXCL11 is produced by a variety of cells, including immune cells such as T cells, natural killer cells, and macrophages, as well as endothelial cells and fibroblasts. It is induced by a variety of stimuli, including interferon-gamma (IFN-gamma), interleukin-12 (IL-12), and lipopolysaccharide (LPS). CXCL11 functions by binding to specific receptors on the surface of immune cells, such as CXCR3, which is expressed on T cells, natural killer cells, and other immune cells. This binding causes the cells to change shape and move towards the source of the chemokine, allowing them to migrate to areas of the body where they are needed to fight infection or injury. In the medical field, CXCL11 is often studied in the context of various diseases and conditions, including infectious diseases, autoimmune diseases, and cancer. For example, CXCL11 has been shown to play a role in the recruitment of immune cells to the site of infection, and it has been implicated in the development of certain types of cancer, such as lung cancer and melanoma. It is also being investigated as a potential therapeutic target for the treatment of these diseases.
Monocyte chemoattractant proteins (MCPs) are a family of small proteins that are produced by various cells in the body, including immune cells, endothelial cells, and fibroblasts. These proteins play a crucial role in the recruitment of monocytes, a type of white blood cell, to sites of inflammation or injury. MCPs function by binding to specific receptors on the surface of monocytes, which triggers a signaling cascade that leads to the activation and migration of these cells towards the site of inflammation. This process is known as chemotaxis. There are several different types of MCPs, including MCP-1, MCP-2, MCP-3, MCP-4, and MCP-5, each with its own specific properties and functions. MCPs are also involved in other physiological processes, such as the regulation of angiogenesis (the formation of new blood vessels) and the development of atherosclerosis (the buildup of plaque in the arteries). In the medical field, MCPs are often studied as potential biomarkers for various diseases, including inflammatory disorders, cardiovascular disease, and cancer. They are also being investigated as potential therapeutic targets for the treatment of these conditions.
Chemotaxis, leukocyte refers to the movement of white blood cells (leukocytes) in response to chemical signals in the body. These chemical signals, also known as chemokines, are released by damaged or infected cells, as well as by immune cells themselves. Chemotaxis allows leukocytes to move towards the site of inflammation or infection, where they can help to fight off pathogens and promote tissue repair. This process is an important part of the immune response and plays a critical role in maintaining overall health and wellbeing.
Chemokine CXCL2, also known as neutrophil chemotactic factor 2 (NCF2) or macrophage inflammatory protein 2 (MIP-2), is a small protein that plays a crucial role in the immune response. It is a member of the CXC chemokine family, which is a group of proteins that regulate the movement of immune cells, such as neutrophils and macrophages, to sites of inflammation or infection. CXCL2 is produced by a variety of cells, including monocytes, macrophages, and endothelial cells, in response to inflammatory stimuli such as bacterial or viral infections, tissue damage, or injury. It acts as a chemoattractant, drawing immune cells to the site of inflammation by binding to specific receptors on their surface. Once CXCL2 binds to its receptors, it triggers a signaling cascade that leads to the activation and migration of immune cells towards the site of inflammation. This process is essential for the clearance of pathogens and the resolution of inflammation. In addition to its role in the immune response, CXCL2 has been implicated in a variety of other physiological processes, including wound healing, angiogenesis, and cancer progression.
Receptors, Interleukin-8B (IL-8B) are a type of protein receptor found on the surface of certain cells in the immune system. These receptors are activated by the binding of interleukin-8B (IL-8B), a type of cytokine, which is a signaling molecule that plays a role in regulating immune responses. IL-8B receptors are primarily expressed on neutrophils, a type of white blood cell that plays a key role in the body's defense against infection. When IL-8B binds to its receptor on a neutrophil, it triggers a signaling cascade that leads to the activation and recruitment of the neutrophil to the site of infection or inflammation. IL-8B receptors are also expressed on other immune cells, including monocytes, macrophages, and T cells, although to a lesser extent. Activation of these receptors on these cells can also contribute to immune responses, although the specific effects depend on the cell type and the context in which the receptors are activated. Overall, IL-8B receptors play an important role in regulating immune responses and are a key target for the development of therapies for a variety of inflammatory and infectious diseases.
Chemokine CXCL5, also known as interleukin-8 (IL-8), is a type of protein that plays a role in the immune system. It is a chemokine, which means that it is a type of signaling molecule that helps to direct the movement of immune cells to specific areas of the body where they are needed. CXCL5 is produced by a variety of cells, including immune cells such as neutrophils, monocytes, and macrophages, as well as epithelial cells and fibroblasts. It is involved in the recruitment of immune cells to sites of inflammation or infection, and it has been implicated in a number of different diseases, including cancer, chronic obstructive pulmonary disease (COPD), and inflammatory bowel disease (IBD). In the medical field, CXCL5 is often measured in blood or other bodily fluids as a way to assess the activity of the immune system and to monitor the progression of certain diseases. It is also being studied as a potential therapeutic target for the treatment of a variety of conditions, including cancer and inflammatory diseases.
Interleukin-8 (IL-8) is a type of cytokine, which is a signaling molecule that plays a role in regulating the immune system. It is produced by various types of cells, including immune cells such as neutrophils, monocytes, and macrophages, as well as epithelial cells and fibroblasts. IL-8 is primarily involved in the recruitment and activation of neutrophils, which are a type of white blood cell that plays a key role in the body's defense against infection and inflammation. IL-8 binds to receptors on the surface of neutrophils, causing them to migrate to the site of infection or inflammation. It also promotes the production of other pro-inflammatory molecules by neutrophils, which helps to amplify the immune response. IL-8 has been implicated in a variety of inflammatory and autoimmune diseases, including chronic obstructive pulmonary disease (COPD), asthma, rheumatoid arthritis, and inflammatory bowel disease. It is also involved in the development of certain types of cancer, such as lung cancer and ovarian cancer. In the medical field, IL-8 is often measured in blood or other bodily fluids as a marker of inflammation or immune activation. It is also being studied as a potential therapeutic target for the treatment of various diseases, including cancer and inflammatory disorders.
Receptors, CXCR3 are a type of protein receptors found on the surface of certain cells in the immune system. They are activated by a chemical messenger called CXCL10, which is produced by immune cells in response to infection or inflammation. Activation of CXCR3 receptors triggers a signaling cascade within the cell that leads to the recruitment and activation of immune cells, such as T cells and natural killer cells, to the site of infection or inflammation. CXCR3 receptors play a critical role in the immune response to viral infections, such as HIV and influenza, and in the development of certain autoimmune diseases, such as multiple sclerosis and rheumatoid arthritis.
Receptors, CCR2 are a type of cell surface receptors that are expressed on various immune cells, including monocytes, macrophages, and dendritic cells. These receptors are activated by a chemokine called CCL2 (also known as MCP-1), which is produced by various cells in response to inflammation or injury. When CCR2 receptors are activated by CCL2, they trigger a signaling cascade within the cell that leads to the recruitment and activation of immune cells to the site of inflammation or injury. This process is important for the body's immune response to infections, tissue damage, and other types of stress. However, excessive activation of CCR2 receptors and the chemokine CCL2 has been implicated in the development of various inflammatory and autoimmune diseases, such as atherosclerosis, rheumatoid arthritis, and multiple sclerosis. Therefore, targeting CCR2 receptors has become an area of active research for the development of new therapies for these diseases.
Chemokine CCL17, also known as TARC (Thymus and Activation-Related Chemokine), is a type of chemokine that plays a role in the immune system. It is a small protein that is produced by various cells, including T cells, B cells, and dendritic cells, and is involved in the recruitment and activation of immune cells, particularly T cells, to sites of inflammation or infection. CCL17 is a chemoattractant, meaning that it attracts immune cells to a specific location in the body. It does this by binding to specific receptors on the surface of immune cells, which triggers a signaling cascade that leads to the movement of the cells towards the source of the chemokine. CCL17 has been implicated in a number of different diseases and conditions, including asthma, atopic dermatitis, and certain types of cancer. In asthma, for example, CCL17 is thought to play a role in the recruitment of T cells to the airways, which can contribute to inflammation and airway remodeling. In atopic dermatitis, CCL17 is thought to contribute to the recruitment of immune cells to the skin, which can lead to itching and inflammation. In cancer, CCL17 has been shown to promote the growth and spread of certain types of tumors by recruiting immune cells to the tumor site and promoting angiogenesis, the formation of new blood vessels.
Receptors, CCR1 are a type of cell surface receptor protein that belongs to the CC chemokine receptor family. These receptors are expressed on various immune cells, including monocytes, macrophages, and T cells, and play a role in the recruitment and activation of these cells in response to inflammatory stimuli. The CCR1 receptor is activated by certain chemokines, which are small signaling molecules that help to regulate the movement of immune cells within the body. When activated, CCR1 receptors can trigger a variety of cellular responses, including the production of inflammatory cytokines, the migration of immune cells to sites of inflammation, and the activation of immune cell signaling pathways. In the medical field, the CCR1 receptor is of interest because it has been implicated in a number of inflammatory and immune-related diseases, including asthma, multiple sclerosis, and rheumatoid arthritis. In some cases, drugs that target the CCR1 receptor have been developed as potential treatments for these conditions.
Chemokine CCL19, also known as Exodus-2, is a type of chemokine protein that plays a role in the immune system. It is a small signaling molecule that is produced by various cells in the body, including immune cells such as dendritic cells and T cells. CCL19 is involved in the recruitment and migration of immune cells to specific areas of the body, such as the lymph nodes and the spleen. It does this by binding to specific receptors on the surface of immune cells, which triggers a signaling cascade that leads to the movement of the cells towards the source of the chemokine. In the medical field, CCL19 is of interest because it has been implicated in a number of different diseases and conditions, including cancer, autoimmune disorders, and infectious diseases. For example, CCL19 has been shown to play a role in the spread of cancer cells to other parts of the body, and it may also be involved in the development of certain autoimmune diseases such as multiple sclerosis. As such, CCL19 is a potential target for the development of new therapies for these conditions.
Chemotactic factors are chemical substances that attract cells towards them. In the medical field, chemotactic factors play a crucial role in the immune response, where they help to direct immune cells to the site of infection or inflammation. Chemotactic factors are produced by various cells, including immune cells, endothelial cells, and fibroblasts. They can be proteins, peptides, or lipids, and they bind to specific receptors on the surface of immune cells, triggering a signaling cascade that leads to cell migration. Examples of chemotactic factors in the immune response include chemokines, which are a type of cytokine that attract immune cells such as neutrophils, monocytes, and lymphocytes to the site of infection or inflammation. Other examples include interleukins, growth factors, and complement proteins. Understanding the role of chemotactic factors in the immune response is important for developing new treatments for infectious diseases, autoimmune disorders, and cancer.
Chemokine CCL21 is a type of protein that plays a role in the immune system. It is also known as Exodus-2, 6Ckine, and CC chemokine ligand 21. CCL21 is produced by cells in the lymphatic system and is involved in the recruitment and migration of immune cells, such as T cells and B cells, to specific areas of the body where they are needed. It does this by binding to specific receptors on the surface of these cells, which triggers a signaling cascade that leads to their movement. CCL21 is also involved in the development and maintenance of immune system tissues, such as lymph nodes and the spleen. In the medical field, CCL21 is being studied as a potential target for the treatment of various diseases, including cancer, autoimmune disorders, and infectious diseases.
Chemokine CCL8, also known as macrophage inflammatory protein 1 alpha (MIP-1α), is a small protein that plays a role in the immune system. It is a type of chemokine, which are proteins that help to direct the movement of immune cells to specific areas of the body in response to infection or injury. CCL8 is produced by a variety of cells, including macrophages, monocytes, and endothelial cells, in response to inflammatory stimuli. It functions by binding to specific receptors on the surface of immune cells, such as T cells and monocytes, and guiding them to the site of inflammation. CCL8 has been implicated in a number of different diseases and conditions, including asthma, chronic obstructive pulmonary disease (COPD), and certain types of cancer. It is also involved in the recruitment of immune cells to the site of infection or injury, and plays a role in the development of inflammation and tissue damage. Overall, CCL8 is an important molecule in the immune system that helps to regulate the movement of immune cells and contribute to the body's response to infection and injury.
Chemokine CCL11, also known as eotaxin-1, is a type of protein that plays a role in the immune system. It is a chemokine, which is a type of signaling molecule that helps to direct the movement of immune cells to specific areas of the body in response to infection or injury. CCL11 is primarily produced by cells in the lung and is involved in the recruitment of eosinophils, a type of white blood cell, to the lung. Eosinophils play a role in the immune response to parasitic infections and in allergic reactions, such as asthma. CCL11 is also involved in the recruitment of other immune cells, such as T cells and monocytes, to the lung. In the medical field, CCL11 is often studied in the context of asthma and other allergic diseases, as well as in the development of new treatments for these conditions. It is also being studied as a potential target for cancer therapy, as it has been found to be overexpressed in some types of cancer.
Chemotaxis is a process by which cells move in response to chemical gradients. In the medical field, chemotaxis is an important mechanism that cells use to migrate to specific locations in the body in response to chemical signals. For example, immune cells such as neutrophils and macrophages use chemotaxis to migrate to sites of infection or inflammation. In this way, chemotaxis plays a critical role in the body's immune response.
Chemokine CCL22, also known as macrophage inflammatory protein 13 (MIP-13), is a type of chemokine protein that plays a role in the immune system. It is produced by various cells, including macrophages, dendritic cells, and T cells, and is involved in the recruitment and activation of immune cells to sites of inflammation or infection. CCL22 is a small protein that binds to specific receptors on the surface of immune cells, such as CCR4, and acts as a chemoattractant, guiding these cells to the site of inflammation. It has been implicated in a number of immune-related disorders, including asthma, allergies, and certain types of cancer. In the medical field, CCL22 is often studied as a potential target for the development of new therapies for these and other conditions. For example, drugs that block the interaction between CCL22 and its receptors have been shown to reduce inflammation and improve symptoms in animal models of asthma and other immune disorders.
Monokines are a type of cytokine, which are signaling molecules secreted by a single type of cell. Monokines are produced by various immune cells, such as macrophages, monocytes, and dendritic cells, in response to infection, inflammation, or other stimuli. They play a role in regulating immune responses, including the recruitment and activation of other immune cells, the production of antibodies, and the regulation of inflammation. Examples of monokines include interleukin-1 (IL-1), tumor necrosis factor-alpha (TNF-alpha), and interferon-gamma (IFN-gamma).
Chemokine CXCL12, also known as stromal cell-derived factor-1 (SDF-1), is a small protein that plays a crucial role in the recruitment and migration of immune cells to specific areas of the body. It is a member of the chemokine family of proteins, which are responsible for directing the movement of cells in response to chemical signals. CXCL12 is primarily produced by cells in the bone marrow, liver, and other tissues, and it is released in response to various stimuli, including inflammation, injury, and infection. It acts by binding to specific receptors on the surface of immune cells, such as T cells, B cells, and monocytes, and guiding them to the site of injury or infection. CXCL12 is also involved in the development and maintenance of the immune system, as well as in the regulation of angiogenesis (the formation of new blood vessels). It has been implicated in a variety of diseases, including cancer, autoimmune disorders, and infectious diseases, and it is a target for the development of new therapies.
Inflammation is a complex biological response of the body to harmful stimuli, such as pathogens, damaged cells, or irritants. It is a protective mechanism that helps to eliminate the cause of injury, remove damaged tissue, and initiate the healing process. Inflammation involves the activation of immune cells, such as white blood cells, and the release of chemical mediators, such as cytokines and prostaglandins. This leads to the characteristic signs and symptoms of inflammation, including redness, heat, swelling, pain, and loss of function. Inflammation can be acute or chronic. Acute inflammation is a short-term response that lasts for a few days to a few weeks and is usually beneficial. Chronic inflammation, on the other hand, is a prolonged response that lasts for months or years and can be harmful if it persists. Chronic inflammation is associated with many diseases, including cancer, cardiovascular disease, and autoimmune disorders.
Chemokine CCL1, also known as macrophage inflammatory protein 1 alpha (MIP-1α), is a type of chemokine protein that plays a role in the immune system. It is produced by various cells, including macrophages, monocytes, and T cells, and is involved in the recruitment and activation of immune cells to sites of inflammation or infection. CCL1 is a small protein that binds to specific receptors on the surface of immune cells, triggering a signaling cascade that leads to the movement of the cells towards the source of the chemokine. This process is known as chemotaxis. In the context of the medical field, CCL1 has been studied for its potential role in various diseases, including cancer, autoimmune disorders, and infectious diseases. For example, high levels of CCL1 have been associated with the progression of certain types of cancer, such as breast and lung cancer. Additionally, CCL1 has been shown to play a role in the recruitment and activation of immune cells in autoimmune disorders such as rheumatoid arthritis and multiple sclerosis. Overall, CCL1 is an important molecule in the immune system and its study may provide insights into the development of new treatments for various diseases.
Receptors, CCR5, are a type of cell surface receptor protein that are expressed on the surface of certain immune cells, such as T cells and macrophages. These receptors are part of the chemokine receptor family and are activated by certain chemokines, which are signaling molecules that help to regulate the movement and function of immune cells. The CCR5 receptor plays an important role in the immune response to HIV (human immunodeficiency virus), which targets and destroys CD4+ T cells, a type of immune cell that expresses CCR5 on its surface. HIV uses the CCR5 receptor to enter and infect these cells. As a result, individuals who lack functional CCR5 receptors (due to a genetic mutation) are resistant to HIV infection. In addition to its role in HIV infection, the CCR5 receptor has been implicated in a variety of other immune-related disorders, including multiple sclerosis, rheumatoid arthritis, and inflammatory bowel disease. As such, the CCR5 receptor is an important target for the development of new therapies for these conditions.
Receptors, Interleukin-8A, also known as CXCR1 and CXCR2, are a type of protein receptor found on the surface of certain cells in the immune system. These receptors are activated by a signaling molecule called interleukin-8 (IL-8), which is produced by immune cells in response to infection or injury. IL-8 plays an important role in the body's immune response by recruiting immune cells to the site of infection or injury. When IL-8 binds to its receptors on immune cells, it triggers a signaling cascade that leads to the activation and migration of these cells to the site of inflammation. Receptors, Interleukin-8A are expressed on a variety of immune cells, including neutrophils, monocytes, and macrophages. They are also found on some non-immune cells, such as epithelial cells and fibroblasts. Abnormalities in the function or expression of these receptors have been linked to a number of diseases, including inflammatory disorders, cancer, and cardiovascular disease. For example, mutations in the gene that encodes for CXCR1 or CXCR2 can lead to a condition called chronic neutrophilic leukemia, which is characterized by an overproduction of neutrophils.
In the medical field, "Cells, Cultured" refers to cells that have been grown and maintained in a controlled environment outside of their natural biological context, typically in a laboratory setting. This process is known as cell culture and involves the isolation of cells from a tissue or organism, followed by their growth and proliferation in a nutrient-rich medium. Cultured cells can be derived from a variety of sources, including human or animal tissues, and can be used for a wide range of applications in medicine and research. For example, cultured cells can be used to study the behavior and function of specific cell types, to develop new drugs and therapies, and to test the safety and efficacy of medical products. Cultured cells can be grown in various types of containers, such as flasks or Petri dishes, and can be maintained at different temperatures and humidity levels to optimize their growth and survival. The medium used to culture cells typically contains a combination of nutrients, growth factors, and other substances that support cell growth and proliferation. Overall, the use of cultured cells has revolutionized medical research and has led to many important discoveries and advancements in the field of medicine.
Receptors, CCR3 are a type of cell surface receptor that belongs to the chemokine receptor family. They are primarily expressed on immune cells, such as eosinophils, basophils, and mast cells, and play a role in the recruitment and activation of these cells in response to certain chemical signals, such as chemokines. CCR3 receptors are involved in a variety of physiological processes, including inflammation, allergic responses, and the immune response to parasites. They are also implicated in the development of certain diseases, such as asthma, chronic obstructive pulmonary disease (COPD), and certain types of cancer. In the medical field, CCR3 receptors are often targeted in the development of new drugs for the treatment of these conditions. For example, drugs that block CCR3 receptors can help to reduce inflammation and allergic responses, and may be useful in the treatment of asthma and COPD.
Chemokine CCL24, also known as eotaxin-2, is a type of protein that plays a role in the immune system. It is a chemokine, which means that it is a signaling molecule that helps to direct the movement of immune cells, such as eosinophils, to specific areas of the body where they are needed. Eotaxin-2 is primarily produced by cells in the skin, lungs, and other tissues, and it is thought to play a role in the recruitment of eosinophils to these areas in response to inflammation or allergic reactions. Eosinophils are a type of white blood cell that are involved in the immune response to parasites and allergens, and they are also involved in the development of certain types of asthma and other inflammatory diseases. In the medical field, chemokine CCL24 is sometimes used as a diagnostic marker for certain conditions, such as asthma and other allergic diseases, and it is also being studied as a potential therapeutic target for the treatment of these conditions.
In the medical field, cell movement refers to the ability of cells to move from one location to another within a tissue or organism. This movement can occur through various mechanisms, including crawling, rolling, and sliding, and is essential for many physiological processes, such as tissue repair, immune response, and embryonic development. There are several types of cell movement, including: 1. Chemotaxis: This is the movement of cells in response to chemical gradients, such as the concentration of a signaling molecule. 2. Haptotaxis: This is the movement of cells in response to physical gradients, such as the stiffness or topography of a substrate. 3. Random walk: This is the movement of cells in a seemingly random manner, which can be influenced by factors such as cell adhesion and cytoskeletal dynamics. 4. Amoeboid movement: This is the movement of cells that lack a well-defined cytoskeleton and rely on changes in cell shape and adhesion to move. Understanding cell movement is important for many medical applications, including the development of new therapies for diseases such as cancer, the study of tissue regeneration and repair, and the design of new materials for tissue engineering and regenerative medicine.
Chemokine CXCL6, also known as fractalkine, is a type of chemokine protein that plays a role in the immune system. It is expressed by a variety of cell types, including endothelial cells, smooth muscle cells, and macrophages, and is involved in the recruitment and activation of immune cells, such as neutrophils and monocytes, to sites of inflammation or injury. CXCL6 is a chemotactic factor, meaning that it attracts immune cells to specific locations in the body. It is also involved in the regulation of angiogenesis, the formation of new blood vessels, and has been implicated in the development of various diseases, including atherosclerosis, cancer, and inflammatory bowel disease. In the medical field, CXCL6 is often studied as a potential therapeutic target for the treatment of various diseases, as well as a biomarker for disease progression or response to treatment.
In the medical field, RNA, Messenger (mRNA) refers to a type of RNA molecule that carries genetic information from DNA in the nucleus of a cell to the ribosomes, where proteins are synthesized. During the process of transcription, the DNA sequence of a gene is copied into a complementary RNA sequence called messenger RNA (mRNA). This mRNA molecule then leaves the nucleus and travels to the cytoplasm of the cell, where it binds to ribosomes and serves as a template for the synthesis of a specific protein. The sequence of nucleotides in the mRNA molecule determines the sequence of amino acids in the protein that is synthesized. Therefore, changes in the sequence of nucleotides in the mRNA molecule can result in changes in the amino acid sequence of the protein, which can affect the function of the protein and potentially lead to disease. mRNA molecules are often used in medical research and therapy as a way to introduce new genetic information into cells. For example, mRNA vaccines work by introducing a small piece of mRNA that encodes for a specific protein, which triggers an immune response in the body.
Chemokine CX3CL1, also known as fractalkine, is a type of chemokine that plays a role in the recruitment and migration of immune cells to sites of inflammation or infection. It is expressed on the surface of various cell types, including endothelial cells, neurons, and microglia, and is involved in the regulation of immune cell trafficking and tissue repair. CX3CL1 binds to its receptor, CX3CR1, which is expressed on the surface of immune cells such as monocytes, macrophages, and T cells. Activation of CX3CR1 by CX3CL1 has been shown to promote the migration of immune cells towards the site of inflammation, as well as to modulate immune cell function and contribute to the resolution of inflammation. In addition, CX3CL1 has been implicated in various diseases, including neurodegenerative disorders, cardiovascular disease, and cancer.
Receptors, CCR10 are a type of cell surface receptor protein that are expressed on certain immune cells, such as T cells and B cells. They are activated by a specific chemokine called CCL27, which is produced by cells in the skin and other tissues. Activation of CCR10 receptors by CCL27 has been shown to play a role in the recruitment of immune cells to the skin, and is thought to be involved in the development of certain skin conditions, such as atopic dermatitis.
Receptors, CXCR4 are a type of protein found on the surface of certain cells in the human body. These proteins are known as chemokine receptors, and they play a role in regulating the movement of cells within the body. Specifically, CXCR4 receptors are activated by a chemical messenger called CXCL12, which is produced by cells in various tissues throughout the body. When CXCR4 receptors are activated by CXCL12, they trigger a signaling cascade within the cell that can lead to a variety of cellular responses, including changes in cell migration, proliferation, and survival. In the medical field, CXCR4 receptors and their interactions with CXCL12 are of interest because they have been implicated in a number of different diseases and conditions, including cancer, HIV infection, and cardiovascular disease.
Receptors, Cytokine are proteins that are present on the surface of cells and are responsible for binding to specific cytokines, which are signaling molecules that play a crucial role in regulating immune responses, cell growth, and differentiation. Cytokine receptors are typically found on the surface of immune cells, such as T cells and B cells, as well as on other cell types, such as endothelial cells and fibroblasts. When a cytokine binds to its specific receptor, it triggers a signaling cascade within the cell that can lead to a variety of cellular responses, such as the activation or suppression of immune cells, the promotion of cell growth or differentiation, or the regulation of inflammation. Dysregulation of cytokine signaling can contribute to a variety of diseases, including autoimmune disorders, cancer, and infectious diseases. Therefore, understanding the function and regulation of cytokine receptors is an important area of research in the medical field.
Chemokine CXCL13, also known as B lymphocyte chemoattractant 1 (BCA-1) or B cell-attracting chemokine 1 (BCA-1), is a type of chemokine that plays a crucial role in the immune system. It is primarily produced by stromal cells, such as follicular dendritic cells and astrocytes, and is involved in the recruitment and retention of B cells in the lymphoid follicles of secondary lymphoid organs, such as the lymph nodes and spleen. CXCL13 is a potent chemoattractant for B cells, and it is believed to play a key role in the formation and maintenance of the germinal centers within lymphoid follicles. These centers are sites of intense B cell proliferation and differentiation, where B cells undergo somatic hypermutation and affinity maturation to generate high-affinity antibodies. In addition to its role in B cell biology, CXCL13 has also been implicated in the pathogenesis of several autoimmune diseases, such as systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA), as well as in the development of certain types of cancer, such as non-Hodgkin's lymphoma (NHL) and multiple myeloma (MM).
Intercellular signaling peptides and proteins are molecules that are secreted by cells and act as messengers to communicate with other cells. These molecules can be hormones, growth factors, cytokines, or other signaling molecules that are capable of transmitting information between cells. They play a crucial role in regulating various physiological processes, such as cell growth, differentiation, and apoptosis, as well as immune responses and inflammation. In the medical field, understanding the function and regulation of intercellular signaling peptides and proteins is important for developing new treatments for various diseases and disorders, including cancer, autoimmune diseases, and neurological disorders.
Chemokine CCL20, also known as macrophage inflammatory protein 3 alpha (MIP-3α), is a small protein that plays a role in the immune system. It is a type of chemokine, which are signaling molecules that help to direct the movement of immune cells to specific areas of the body in response to infection or injury. CCL20 is produced by a variety of cells, including macrophages, dendritic cells, and epithelial cells. It is involved in the recruitment of immune cells, such as T cells and B cells, to the lymph nodes and other areas of the body where they can help to fight infection. In the context of the medical field, CCL20 has been studied in relation to a number of different conditions, including cancer, autoimmune diseases, and infectious diseases. For example, CCL20 has been shown to play a role in the development and progression of certain types of cancer, such as breast cancer and lung cancer. It has also been implicated in the pathogenesis of autoimmune diseases, such as multiple sclerosis, and in the recruitment of immune cells to sites of infection. Overall, CCL20 is an important molecule in the immune system that helps to regulate the movement of immune cells and plays a role in the body's response to infection and injury.
Receptors, CCR4, are a type of cell surface receptor that belongs to the CC chemokine receptor family. These receptors are expressed on various immune cells, including T cells, eosinophils, and basophils, and play a role in the recruitment and activation of these cells in response to certain chemokines. The CCR4 receptor is activated by chemokines such as CCL17 and CCL22, which are produced by various cells in the body, including immune cells and epithelial cells. Activation of CCR4 receptors on immune cells leads to their migration to sites of inflammation or infection, where they can help to fight off pathogens or clear damaged tissue. In addition to their role in immune cell recruitment and activation, CCR4 receptors have also been implicated in various diseases, including asthma, allergies, and certain types of cancer. For example, high levels of CCR4 expression on T cells have been associated with poor prognosis in patients with certain types of leukemia and lymphoma.
Receptors, CCR7 are a type of cell surface receptor protein that are expressed on the surface of certain immune cells, such as T cells and dendritic cells. These receptors are activated by a chemical messenger called chemokine (C-C motif) ligand 19 (CCL19) and chemokine (C-C motif) ligand 21 (CCL21), which are produced by cells in the lymphatic system and the spleen. When CCR7 receptors are activated by CCL19 or CCL21, they trigger a signaling cascade within the immune cell that promotes its movement towards the site of infection or inflammation. This process, known as chemotaxis, is an important mechanism for the recruitment of immune cells to the site of an infection or injury. In addition to their role in immune cell trafficking, CCR7 receptors have also been implicated in the development and progression of certain types of cancer, such as breast cancer and non-small cell lung cancer. In these cases, the overexpression of CCR7 receptors on cancer cells can promote their migration and spread to other parts of the body, making them more difficult to treat.
Receptors, CCR8 are a type of cell surface receptors that are expressed on various immune cells, including T cells, B cells, and dendritic cells. These receptors are activated by the chemokine CCL1, also known as eotaxin-1, which is produced by various cells in the body, including epithelial cells, fibroblasts, and mast cells. The activation of CCR8 receptors by CCL1 has been shown to play a role in the recruitment and activation of immune cells, particularly eosinophils, to sites of inflammation. This is important in the context of allergic reactions, where eosinophils are involved in the release of inflammatory mediators that contribute to symptoms such as itching, swelling, and airway constriction. In addition to their role in allergic reactions, CCR8 receptors have also been implicated in the pathogenesis of other inflammatory diseases, such as rheumatoid arthritis and multiple sclerosis. Therefore, targeting CCR8 receptors may be a potential therapeutic strategy for the treatment of these conditions.
Tumor Necrosis Factor-alpha (TNF-alpha) is a cytokine, a type of signaling protein, that plays a crucial role in the immune response and inflammation. It is produced by various cells in the body, including macrophages, monocytes, and T cells, in response to infection, injury, or other stimuli. TNF-alpha has multiple functions in the body, including regulating the immune response, promoting cell growth and differentiation, and mediating inflammation. It can also induce programmed cell death, or apoptosis, in some cells, which can be beneficial in fighting cancer. However, excessive or prolonged TNF-alpha production can lead to chronic inflammation and tissue damage, which can contribute to the development of various diseases, including autoimmune disorders, inflammatory bowel disease, and certain types of cancer. In the medical field, TNF-alpha is often targeted in the treatment of these conditions. For example, drugs called TNF inhibitors, such as infliximab and adalimumab, are used to block the action of TNF-alpha and reduce inflammation in patients with rheumatoid arthritis, Crohn's disease, and other inflammatory conditions.
Beta-thromboglobulin (β-TG) is a plasma protein that plays a role in the coagulation cascade, which is the series of chemical reactions that ultimately leads to the formation of a blood clot. It is produced by platelets, which are small blood cells that are involved in blood clotting. When platelets are activated, they release β-TG, which acts as a marker of platelet activation. It is also involved in the formation of platelet aggregates, which are clusters of platelets that stick together to form a plug at the site of a blood vessel injury. In the medical field, β-TG is often used as a diagnostic marker for platelet activation and thrombosis, which is the formation of a blood clot in a blood vessel. Elevated levels of β-TG in the blood can indicate a higher risk of thrombosis, while low levels may indicate a deficiency in platelet function. It is also used as a marker of inflammation and tissue damage.
Interferon-gamma (IFN-γ) is a type of cytokine, which is a signaling molecule that plays a crucial role in the immune system. It is produced by various immune cells, including T cells, natural killer cells, and macrophages, in response to viral or bacterial infections, as well as in response to certain types of cancer. IFN-γ has a wide range of effects on the immune system, including the activation of macrophages and other immune cells, the inhibition of viral replication, and the promotion of T cell differentiation and proliferation. It also plays a role in the regulation of the immune response, helping to prevent excessive inflammation and tissue damage. In the medical field, IFN-γ is used as a therapeutic agent in the treatment of certain types of cancer, such as Hodgkin's lymphoma and multiple myeloma. It is also being studied as a potential treatment for other conditions, such as autoimmune diseases and viral infections.
Dendritic cells are a type of immune cell that plays a crucial role in the body's immune response. They are found in various tissues throughout the body, including the skin, lymph nodes, and mucous membranes. Dendritic cells are responsible for capturing and processing antigens, which are foreign substances that can trigger an immune response. They do this by engulfing and breaking down antigens, and then presenting them to other immune cells, such as T cells, in a way that activates the immune response. Dendritic cells are also involved in the regulation of immune responses, helping to prevent the body from overreacting to harmless substances and to maintain immune tolerance to self-antigens. In the medical field, dendritic cells are being studied for their potential use in cancer immunotherapy. They can be genetically modified to recognize and attack cancer cells, and are being tested in clinical trials as a way to treat various types of cancer.
In the medical field, "Disease Models, Animal" refers to the use of animals to study and understand human diseases. These models are created by introducing a disease or condition into an animal, either naturally or through experimental manipulation, in order to study its progression, symptoms, and potential treatments. Animal models are used in medical research because they allow scientists to study diseases in a controlled environment and to test potential treatments before they are tested in humans. They can also provide insights into the underlying mechanisms of a disease and help to identify new therapeutic targets. There are many different types of animal models used in medical research, including mice, rats, rabbits, dogs, and monkeys. Each type of animal has its own advantages and disadvantages, and the choice of model depends on the specific disease being studied and the research question being addressed.
NF-kappa B (Nuclear Factor kappa B) is a transcription factor that plays a critical role in regulating the immune response, inflammation, and cell survival. It is a complex of proteins that is found in the cytoplasm of cells and is activated in response to various stimuli, such as cytokines, bacterial and viral infections, and stress. When activated, NF-kappa B translocates to the nucleus and binds to specific DNA sequences, promoting the expression of genes involved in immune and inflammatory responses. This includes genes encoding for cytokines, chemokines, and adhesion molecules, which help to recruit immune cells to the site of infection or injury. NF-kappa B is also involved in regulating cell survival and apoptosis (programmed cell death). Dysregulation of NF-kappa B signaling has been implicated in a variety of diseases, including cancer, autoimmune disorders, and inflammatory diseases such as rheumatoid arthritis and inflammatory bowel disease.
Chemotactic factors, eosinophil are chemical substances that attract eosinophils, a type of white blood cell, to a specific location in the body. These factors are produced by various cells, including immune cells and cells in the lining of tissues, in response to inflammation or infection. Eosinophils play a role in the immune response to parasitic infections and allergies, and they are also involved in tissue repair and remodeling. Chemotactic factors for eosinophils can be either proteinaceous or lipid-based, and they bind to specific receptors on the surface of eosinophils, guiding them to the site of inflammation or infection.
Lipopolysaccharides (LPS) are a type of complex carbohydrate found on the surface of gram-negative bacteria. They are composed of a lipid A moiety, a core polysaccharide, and an O-specific polysaccharide. LPS are important components of the bacterial cell wall and play a role in the innate immune response of the host. In the medical field, LPS are often studied in the context of sepsis, a life-threatening condition that occurs when the body's response to an infection causes widespread inflammation. LPS can trigger a strong immune response in the host, leading to the release of pro-inflammatory cytokines and other mediators that can cause tissue damage and organ failure. As a result, LPS are often used as a model for studying the pathophysiology of sepsis and for developing new treatments for this condition. LPS are also used in research as a tool for studying the immune system and for developing vaccines against bacterial infections. They can be purified from bacterial cultures and used to stimulate immune cells in vitro or in animal models, allowing researchers to study the mechanisms of immune responses to bacterial pathogens. Additionally, LPS can be used as an adjuvant in vaccines to enhance the immune response to the vaccine antigen.
In the medical field, a cell line refers to a group of cells that have been derived from a single parent cell and have the ability to divide and grow indefinitely in culture. These cells are typically grown in a laboratory setting and are used for research purposes, such as studying the effects of drugs or investigating the underlying mechanisms of diseases. Cell lines are often derived from cancerous cells, as these cells tend to divide and grow more rapidly than normal cells. However, they can also be derived from normal cells, such as fibroblasts or epithelial cells. Cell lines are characterized by their unique genetic makeup, which can be used to identify them and compare them to other cell lines. Because cell lines can be grown in large quantities and are relatively easy to maintain, they are a valuable tool in medical research. They allow researchers to study the effects of drugs and other treatments on specific cell types, and to investigate the underlying mechanisms of diseases at the cellular level.
Platelet Factor 4 (PF4) is a protein that is produced by platelets, which are small blood cells that play a crucial role in blood clotting. PF4 is a member of a family of proteins called chemokines, which are involved in the recruitment of immune cells to sites of injury or infection. PF4 is primarily known for its role in the immune response to bacterial infections. When bacteria enter the bloodstream, they can trigger the release of PF4 from platelets, which then binds to the bacteria and helps to recruit immune cells to the site of infection. PF4 also has anticoagulant properties, meaning that it can help to prevent blood clots from forming. In addition to its role in the immune response and blood clotting, PF4 has been implicated in a number of other medical conditions. For example, high levels of PF4 have been associated with certain autoimmune disorders, such as lupus and rheumatoid arthritis. PF4 has also been linked to the development of certain types of cancer, including lung cancer and ovarian cancer. Overall, PF4 is an important protein that plays a role in a variety of physiological processes, including immune response, blood clotting, and cancer development.
Receptors, CCR6 are a type of cell surface receptors that are expressed on certain immune cells, such as T cells and dendritic cells. These receptors are activated by a chemical messenger called CCL20, which is produced by cells in the body in response to infection or inflammation. CCR6 receptors play a role in the recruitment and activation of immune cells to sites of infection or inflammation. They are also involved in the development and function of certain types of immune cells, such as Th17 cells, which are important for fighting off certain types of infections. Abnormalities in the function or expression of CCR6 receptors have been linked to a number of diseases, including autoimmune disorders, allergies, and certain types of cancer. For example, some studies have suggested that CCR6 receptors may play a role in the development of multiple sclerosis, a chronic autoimmune disorder that affects the central nervous system.
Receptors, CXCR refer to a family of G protein-coupled receptors (GPCRs) that are activated by chemokines, a type of signaling molecule that plays a crucial role in immune cell trafficking and inflammation. The CXCR receptors are expressed on the surface of various immune cells, including T cells, B cells, and natural killer cells, and are involved in the recruitment and activation of these cells in response to infection or injury. There are several different CXCR receptors, including CXCR1, CXCR2, CXCR3, CXCR4, and CXCR5, each of which is activated by a specific subset of chemokines. Activation of these receptors leads to the activation of intracellular signaling pathways that regulate various cellular processes, including cell migration, proliferation, and differentiation. Abnormalities in the function or expression of CXCR receptors have been implicated in a variety of diseases, including cancer, autoimmune disorders, and infectious diseases. As such, the CXCR receptors are an important target for the development of new therapeutic agents for the treatment of these conditions.
Receptors, CCR (Chemokine Receptors, CCR) are a family of cell surface receptors that are involved in the immune system's response to infection and inflammation. They are activated by chemokines, which are small signaling molecules that help to direct immune cells to specific areas of the body where they are needed. There are several different subtypes of CCR receptors, each of which is activated by a specific chemokine. These receptors are found on a variety of immune cells, including T cells, B cells, macrophages, and dendritic cells. When a chemokine binds to its specific receptor, it triggers a signaling cascade within the cell that leads to changes in cell behavior, such as migration, proliferation, or activation. The CCR receptors play an important role in the immune response to infection and inflammation, and they are also involved in the development of certain diseases, such as cancer and autoimmune disorders. Understanding the function of these receptors is important for developing new treatments for these conditions.
Bronchoalveolar Lavage Fluid (BALF) is a type of fluid that is collected from the airways and alveoli of the lungs. It is obtained by washing the airways and alveoli with a sterile saline solution using a bronchoscope, which is a thin, flexible tube that is inserted through the mouth or nose into the airways. BALF is used to diagnose and monitor a variety of lung diseases, including pneumonia, lung infections, lung cancer, and interstitial lung diseases. It can also be used to assess the immune response of the lungs and to detect the presence of foreign substances, such as bacteria, viruses, and fungi. The fluid is usually analyzed in a laboratory to determine the number and type of cells present, as well as the levels of various proteins and other substances. This information can help doctors to diagnose and treat the underlying cause of the patient's symptoms.
Receptors, CXCR5 are a type of protein receptors found on the surface of certain immune cells, such as T cells and B cells. These receptors are activated by a signaling molecule called CXCL13, which is produced by cells in the lymph nodes and other tissues. Activation of CXCR5 receptors helps to guide immune cells to the site of infection or inflammation, and plays a role in the development and maintenance of immune responses. Abnormalities in the function of CXCR5 receptors have been implicated in a number of autoimmune and inflammatory diseases, including lupus and rheumatoid arthritis.
Cell migration inhibition refers to the process of preventing or reducing the movement of cells from one location to another. In the medical field, this concept is often used to study the behavior of cells in various diseases and conditions, such as cancer, inflammation, and wound healing. Cell migration inhibition can be achieved through various mechanisms, including the use of chemical inhibitors, physical barriers, or changes in the extracellular matrix. For example, some drugs can block the activity of enzymes that are involved in cell migration, while others can interfere with the signaling pathways that regulate cell movement. In cancer research, cell migration inhibition is often used as a strategy to prevent the spread of cancer cells to other parts of the body, a process known as metastasis. By blocking cell migration, researchers hope to develop new treatments that can slow down or stop the progression of cancer. Overall, cell migration inhibition is an important concept in the medical field, as it can provide insights into the underlying mechanisms of various diseases and help to identify new therapeutic targets for treatment.
Chemokine CCL27, also known as interleukin-17E (IL-17E), is a type of cytokine that plays a role in the immune system. It is a member of the C-C chemokine family, which is a group of proteins that help to regulate the movement of immune cells within the body. CCL27 is primarily produced by cells of the immune system, including T cells and dendritic cells, and it is involved in the recruitment and activation of immune cells in response to infection or inflammation. It is also involved in the development and function of certain types of immune cells, such as Th17 cells, which play a role in the immune response to pathogens. In the medical field, CCL27 has been studied in relation to a number of different conditions, including psoriasis, atopic dermatitis, and inflammatory bowel disease. It is thought to play a role in the development and progression of these conditions by promoting inflammation and immune cell recruitment to the affected tissues.
Intercellular Adhesion Molecule-1 (ICAM-1) is a protein that plays a crucial role in the immune system and cell signaling. It is expressed on the surface of various cell types, including immune cells, endothelial cells, and epithelial cells. ICAM-1 functions as a receptor for immune cells, allowing them to adhere to and migrate across the endothelial cells that line blood vessels. This process is essential for the immune system to respond to infections and other inflammatory stimuli. ICAM-1 also plays a role in cell signaling, mediating the interaction between cells and their environment. It can be activated by various stimuli, including cytokines, hormones, and growth factors, and can regulate processes such as cell proliferation, differentiation, and apoptosis. In the medical field, ICAM-1 is often studied in the context of various diseases, including autoimmune disorders, cancer, and cardiovascular disease. For example, increased expression of ICAM-1 has been associated with the development and progression of several types of cancer, including breast cancer and lung cancer. Additionally, ICAM-1 has been implicated in the pathogenesis of inflammatory diseases such as rheumatoid arthritis and multiple sclerosis.
Recombinant proteins are proteins that are produced by genetically engineering bacteria, yeast, or other organisms to express a specific gene. These proteins are typically used in medical research and drug development because they can be produced in large quantities and are often more pure and consistent than proteins that are extracted from natural sources. Recombinant proteins can be used for a variety of purposes in medicine, including as diagnostic tools, therapeutic agents, and research tools. For example, recombinant versions of human proteins such as insulin, growth hormones, and clotting factors are used to treat a variety of medical conditions. Recombinant proteins can also be used to study the function of specific genes and proteins, which can help researchers understand the underlying causes of diseases and develop new treatments.
In the medical field, an amino acid sequence refers to the linear order of amino acids in a protein molecule. Proteins are made up of chains of amino acids, and the specific sequence of these amino acids determines the protein's structure and function. The amino acid sequence is determined by the genetic code, which is a set of rules that specifies how the sequence of nucleotides in DNA is translated into the sequence of amino acids in a protein. Each amino acid is represented by a three-letter code, and the sequence of these codes is the amino acid sequence of the protein. The amino acid sequence is important because it determines the protein's three-dimensional structure, which in turn determines its function. Small changes in the amino acid sequence can have significant effects on the protein's structure and function, and this can lead to diseases or disorders. For example, mutations in the amino acid sequence of a protein involved in blood clotting can lead to bleeding disorders.
In the medical field, cell adhesion refers to the process by which cells stick to each other or to a surface. This is an essential process for the proper functioning of tissues and organs in the body. There are several types of cell adhesion, including: 1. Homophilic adhesion: This occurs when cells adhere to each other through the interaction of specific molecules on their surface. 2. Heterophilic adhesion: This occurs when cells adhere to each other through the interaction of different molecules on their surface. 3. Heterotypic adhesion: This occurs when cells adhere to each other through the interaction of different types of cells. 4. Intercellular adhesion: This occurs when cells adhere to each other through the interaction of molecules within the cell membrane. 5. Intracellular adhesion: This occurs when cells adhere to each other through the interaction of molecules within the cytoplasm. Cell adhesion is important for a variety of processes, including tissue development, wound healing, and the immune response. Disruptions in cell adhesion can lead to a variety of medical conditions, including cancer, autoimmune diseases, and inflammatory disorders.
Interleukin-6 (IL-6) is a cytokine, a type of signaling molecule that plays a crucial role in the immune system. It is produced by a variety of cells, including immune cells such as macrophages, monocytes, and T cells, as well as non-immune cells such as fibroblasts and endothelial cells. IL-6 has a wide range of functions in the body, including regulating the immune response, promoting inflammation, and stimulating the growth and differentiation of immune cells. It is also involved in the regulation of metabolism, bone metabolism, and hematopoiesis (the production of blood cells). In the medical field, IL-6 is often measured as a marker of inflammation and is used to diagnose and monitor a variety of conditions, including autoimmune diseases, infections, and cancer. It is also being studied as a potential therapeutic target for the treatment of these conditions, as well as for the management of chronic pain and other conditions.
CD4-positive T-lymphocytes, also known as CD4+ T-cells or T-helper cells, are a type of white blood cell that plays a critical role in the immune system. They are a subset of T-cells that express the CD4 protein on their surface, which allows them to recognize and bind to antigens presented by other immune cells. CD4+ T-cells are involved in many aspects of the immune response, including the activation and proliferation of other immune cells, the production of cytokines (chemical messengers that regulate immune responses), and the regulation of immune tolerance. They are particularly important in the response to infections caused by viruses, such as HIV, and in the development of autoimmune diseases. In HIV infection, the virus specifically targets and destroys CD4+ T-cells, leading to a decline in their numbers and a weakened immune system. This is why CD4+ T-cell count is an important marker of HIV disease progression and treatment response.
Cell adhesion molecules (CAMs) are proteins that mediate the attachment of cells to each other or to the extracellular matrix. They play a crucial role in various physiological processes, including tissue development, wound healing, immune response, and cancer progression. There are several types of CAMs, including cadherins, integrins, selectins, and immunoglobulin superfamily members. Each type of CAM has a unique structure and function, and they can interact with other molecules to form complex networks that regulate cell behavior. In the medical field, CAMs are often studied as potential targets for therapeutic interventions. For example, drugs that block specific CAMs have been developed to treat cancer, autoimmune diseases, and cardiovascular disorders. Additionally, CAMs are used as diagnostic markers to identify and monitor various diseases, including cancer, inflammation, and neurodegenerative disorders.
Receptors, Interleukin are proteins found on the surface of cells that bind to specific molecules called interleukins. Interleukins are a type of cytokine, which are signaling molecules that play a role in regulating immune responses and other cellular processes. When an interleukin binds to its receptor on a cell, it can trigger a variety of cellular responses, such as the activation or suppression of immune cells, the proliferation of cells, or the production of other signaling molecules. Interleukin receptors are important for the proper functioning of the immune system and are the targets of many drugs used to treat immune-related diseases.
Interleukin-1beta (IL-1β) is a type of cytokine, which is a signaling molecule that plays a crucial role in the immune system. It is produced by various types of immune cells, including macrophages, monocytes, and dendritic cells, in response to infection, injury, or inflammation. IL-1β is involved in the regulation of immune responses, including the activation of T cells, B cells, and natural killer cells. It also promotes the production of other cytokines and chemokines, which help to recruit immune cells to the site of infection or injury. In addition to its role in the immune system, IL-1β has been implicated in a variety of inflammatory and autoimmune diseases, including rheumatoid arthritis, inflammatory bowel disease, and multiple sclerosis. It is also involved in the pathogenesis of certain types of cancer, such as breast cancer and ovarian cancer. Overall, IL-1β is a key mediator of inflammation and immune responses, and its dysregulation has been linked to a range of diseases and conditions.
Receptors, cell surface are proteins that are located on the surface of cells and are responsible for receiving signals from the environment. These signals can be chemical, electrical, or mechanical in nature and can trigger a variety of cellular responses. There are many different types of cell surface receptors, including ion channels, G-protein coupled receptors, and enzyme-linked receptors. These receptors play a critical role in many physiological processes, including sensation, communication, and regulation of cellular activity. In the medical field, understanding the function and regulation of cell surface receptors is important for developing new treatments for a wide range of diseases and conditions.
Toll-like receptors (TLRs) are a family of proteins that play a crucial role in the innate immune system. They are expressed on the surface of immune cells, such as macrophages and dendritic cells, and are responsible for recognizing and responding to pathogen-associated molecular patterns (PAMPs), which are molecules that are unique to microorganisms and not found in host cells. When TLRs recognize PAMPs, they trigger a signaling cascade that leads to the activation of immune cells and the production of pro-inflammatory cytokines. This helps to initiate an immune response against the invading pathogen. TLRs are also involved in the recognition of damage-associated molecular patterns (DAMPs), which are molecules that are released by damaged or dying host cells. This can help to trigger an inflammatory response in cases of tissue injury or infection. Overall, TLRs play a critical role in the immune system's ability to detect and respond to pathogens and tissue damage.
Interleukin-1 (IL-1) is a type of cytokine, which is a signaling molecule that plays a crucial role in the immune system. IL-1 is produced by various types of immune cells, including macrophages, monocytes, and dendritic cells, in response to infection, injury, or inflammation. IL-1 has multiple functions in the immune system, including promoting the activation and proliferation of immune cells, enhancing the production of other cytokines, and regulating the inflammatory response. It can also stimulate the production of fever, which helps to fight off infections. In the medical field, IL-1 is often studied in the context of various diseases, including autoimmune disorders, inflammatory bowel disease, and rheumatoid arthritis. It is also being investigated as a potential target for the development of new treatments for these conditions.
Biological markers, also known as biomarkers, are measurable indicators of biological processes, pathogenic processes, or responses to therapeutic interventions. In the medical field, biological markers are used to diagnose, monitor, and predict the progression of diseases, as well as to evaluate the effectiveness of treatments. Biological markers can be found in various biological samples, such as blood, urine, tissue, or body fluids. They can be proteins, genes, enzymes, hormones, metabolites, or other molecules that are associated with a specific disease or condition. For example, in cancer, biological markers such as tumor markers can be used to detect the presence of cancer cells or to monitor the response to treatment. In cardiovascular disease, biological markers such as cholesterol levels or blood pressure can be used to assess the risk of heart attack or stroke. Overall, biological markers play a crucial role in medical research and clinical practice, as they provide valuable information about the underlying biology of diseases and help to guide diagnosis, treatment, and monitoring.
In the medical field, cell communication refers to the process by which cells exchange information and signals with each other. This communication is essential for the proper functioning of the body's tissues and organs, as it allows cells to coordinate their activities and respond to changes in their environment. There are several types of cell communication, including direct communication between neighboring cells, as well as communication through the bloodstream or lymphatic system. Some of the key mechanisms of cell communication include the release of signaling molecules, such as hormones and neurotransmitters, as well as the exchange of ions and other small molecules across cell membranes. Disruptions in cell communication can lead to a variety of medical conditions, including cancer, autoimmune diseases, and neurological disorders. Therefore, understanding the mechanisms of cell communication is an important area of research in medicine, with potential applications in the development of new treatments and therapies.
In the medical field, "Antigens, CD" refers to a group of proteins found on the surface of certain cells in the immune system. These proteins, known as CD antigens, are recognized by other immune cells and play a crucial role in the immune response to infections and diseases. CD antigens are classified into different families based on their structure and function. Some CD antigens are expressed on the surface of immune cells themselves, while others are found on the surface of cells that are targeted by the immune system, such as cancer cells or cells infected with viruses. The identification and characterization of CD antigens has been important for the development of new diagnostic tests and therapies for a variety of diseases, including cancer, autoimmune disorders, and infectious diseases. For example, monoclonal antibodies that target specific CD antigens have been used in cancer immunotherapy to help the immune system recognize and attack cancer cells.
Interleukins are a group of signaling proteins that are produced by various cells of the immune system, including white blood cells, and play a crucial role in regulating immune responses. They are also involved in a wide range of other physiological processes, such as cell growth, differentiation, and apoptosis (programmed cell death). Interleukins are classified into different groups based on their structure and function. Some of the most well-known interleukins include interleukin-1 (IL-1), interleukin-2 (IL-2), interleukin-4 (IL-4), interleukin-6 (IL-6), interleukin-10 (IL-10), and interleukin-12 (IL-12). Interleukins can act locally within tissues or be transported through the bloodstream to other parts of the body. They can also bind to specific receptors on the surface of target cells, triggering a signaling cascade that leads to changes in gene expression and cellular function. In the medical field, interleukins are often used as therapeutic agents to treat a variety of conditions, including autoimmune diseases, cancer, and infections. They can also be used as diagnostic tools to help identify and monitor certain diseases.
Vascular Cell Adhesion Molecule-1 (VCAM-1) is a protein that plays a crucial role in the immune system's response to inflammation and infection. It is expressed on the surface of endothelial cells, which line the inner lining of blood vessels, and is involved in the recruitment of immune cells, such as monocytes and T cells, to sites of inflammation. VCAM-1 binds to a protein called integrin on the surface of immune cells, which triggers a series of signaling events that lead to the adhesion of the immune cells to the endothelial cells. This process is essential for the immune system to mount an effective response to infection or injury, but it can also contribute to the development of chronic inflammation and autoimmune diseases. In addition to its role in immune cell recruitment, VCAM-1 has been implicated in the development of a variety of cardiovascular diseases, including atherosclerosis, hypertension, and heart failure. It is also involved in the progression of certain types of cancer, such as breast and colon cancer. Overall, VCAM-1 is a key player in the complex interplay between the immune system and the vasculature, and its dysregulation has been linked to a range of diseases and conditions.
Case-control studies are a type of observational study used in the medical field to investigate the relationship between an exposure and an outcome. In a case-control study, researchers identify individuals who have experienced a particular outcome (cases) and compare their exposure history to a group of individuals who have not experienced the outcome (controls). The main goal of a case-control study is to determine whether the exposure was a risk factor for the outcome. To do this, researchers collect information about the exposure history of both the cases and the controls and compare the two groups to see if there is a statistically significant difference in the prevalence of the exposure between the two groups. Case-control studies are often used when the outcome of interest is rare, and it is difficult or unethical to conduct a prospective cohort study. However, because case-control studies rely on retrospective data collection, they are subject to recall bias, where participants may not accurately remember their exposure history. Additionally, because case-control studies only provide information about the association between an exposure and an outcome, they cannot establish causality.
In the medical field, "Culture Media, Conditioned" refers to a type of growth medium that has been prepared by adding nutrients and other components to a basic medium, such as agar, to support the growth of specific microorganisms. The term "conditioned" indicates that the medium has been treated or modified in some way to enhance the growth of the target microorganisms. Conditioned culture media are often used in diagnostic microbiology to isolate and identify specific microorganisms from clinical samples, such as blood, urine, or sputum. The medium may be further conditioned by adding specific supplements or antibiotics to inhibit the growth of unwanted microorganisms and promote the growth of the target organism. Overall, conditioned culture media are an important tool in the diagnosis and treatment of infectious diseases, as they allow healthcare professionals to accurately identify the causative agent and select the most effective antimicrobial therapy.
Anti-inflammatory agents are medications that are used to reduce inflammation in the body. Inflammation is a natural response of the immune system to injury or infection, but chronic inflammation can lead to a variety of health problems, including autoimmune diseases, cancer, and cardiovascular disease. Anti-inflammatory agents work by blocking the production of inflammatory molecules, such as prostaglandins and cytokines, which are responsible for causing inflammation. They can also reduce the activity of immune cells that contribute to inflammation. There are several types of anti-inflammatory agents, including nonsteroidal anti-inflammatory drugs (NSAIDs), corticosteroids, and biologic agents. NSAIDs, such as aspirin and ibuprofen, are commonly used to relieve pain and reduce inflammation in conditions such as arthritis and headaches. Corticosteroids, such as prednisone, are powerful anti-inflammatory agents that are used to treat a wide range of conditions, including asthma, allergies, and autoimmune diseases. Biologic agents, such as TNF inhibitors, are a newer class of anti-inflammatory agents that are used to treat autoimmune diseases such as rheumatoid arthritis and Crohn's disease. It is important to note that while anti-inflammatory agents can be effective in reducing inflammation, they can also have side effects and may not be appropriate for everyone. It is important to work with a healthcare provider to determine the best treatment plan for your individual needs.
Coculture techniques refer to the process of growing two or more different cell types together in a single culture dish or flask. This is commonly used in the medical field to study interactions between cells, such as how cancer cells affect normal cells or how immune cells respond to pathogens. Coculture techniques can be used in a variety of ways, including co-culturing cells from different tissues or organs, co-culturing cells with different cell types, or co-culturing cells with microorganisms or other foreign substances. Coculture techniques can also be used to study the effects of drugs or other treatments on cell interactions. Overall, coculture techniques are a valuable tool in the medical field for studying cell interactions and developing new treatments for diseases.
CD8-positive T-lymphocytes, also known as cytotoxic T-cells, are a type of white blood cell that plays a crucial role in the immune system's response to infections and diseases. These cells are a subtype of T-lymphocytes, which are a type of immune cell that plays a central role in cell-mediated immunity. CD8-positive T-lymphocytes are characterized by the presence of a protein called CD8 on their surface, which helps them to recognize and bind to infected cells or cancer cells. Once bound, these cells release toxic substances that can kill the infected or cancerous cells. CD8-positive T-lymphocytes are an important part of the immune system's response to viral infections, such as HIV and herpes, and to some types of cancer. They are also involved in the immune response to bacterial infections and in the regulation of immune responses to prevent autoimmune diseases. In the medical field, CD8-positive T-lymphocytes are often studied as a way to understand the immune system's response to infections and diseases, and to develop new treatments for these conditions.
Cell differentiation is the process by which cells acquire specialized functions and characteristics during development. It is a fundamental process that occurs in all multicellular organisms, allowing cells to differentiate into various types of cells with specific functions, such as muscle cells, nerve cells, and blood cells. During cell differentiation, cells undergo changes in their shape, size, and function, as well as changes in the proteins and other molecules they produce. These changes are controlled by a complex network of genes and signaling pathways that regulate the expression of specific genes in different cell types. Cell differentiation is a critical process for the proper development and function of tissues and organs in the body. It is also involved in tissue repair and regeneration, as well as in the progression of diseases such as cancer, where cells lose their normal differentiation and become cancerous.
Receptors, HIV refers to the proteins on the surface of certain cells in the human immune system that are targeted by the human immunodeficiency virus (HIV). These receptors, known as CD4 receptors and chemokine receptors, play a crucial role in the entry and replication of HIV in the body. Once HIV binds to these receptors, it is able to enter the cell and use its genetic material to produce more copies of itself, leading to the destruction of immune cells and the progression of HIV infection to acquired immunodeficiency syndrome (AIDS).
Uteroglobin is a protein that is produced by the uterine epithelial cells in pregnant women. It is also known as pregnancy-specific protein or PSP. Uteroglobin is a member of the lipocalin family of proteins, which are involved in the transport of small hydrophobic molecules such as fatty acids and steroids. Uteroglobin is primarily produced during pregnancy and is thought to play a role in protecting the developing fetus from infections and other harmful substances. It has also been suggested that uteroglobin may have a role in regulating the immune response in the uterus during pregnancy. In addition to its role in pregnancy, uteroglobin has been found to be elevated in a number of other conditions, including endometriosis, ovarian cancer, and breast cancer. However, the exact function of uteroglobin in these conditions is not yet fully understood.
Interleukin-17 (IL-17) is a cytokine, a type of signaling molecule, that plays a role in the immune system's response to infection and inflammation. It is produced by certain types of immune cells, including T cells and natural killer T cells, and is involved in the recruitment and activation of other immune cells, such as neutrophils and macrophages, to the site of infection or injury. IL-17 is also involved in the development of autoimmune diseases, such as rheumatoid arthritis and psoriasis, where it contributes to inflammation and tissue damage. In addition, IL-17 has been implicated in the pathogenesis of inflammatory bowel disease, multiple sclerosis, and other inflammatory conditions. In the medical field, IL-17 is a target for the development of new therapies for autoimmune diseases and other inflammatory conditions. Inhibitors of IL-17, such as biologic drugs, have been shown to be effective in reducing inflammation and improving symptoms in patients with these conditions.
Angiostatic proteins are a group of proteins that regulate blood vessel formation, also known as angiogenesis. They play a crucial role in maintaining the balance between blood vessel growth and regression, which is essential for normal tissue development, wound healing, and tumor growth. Angiostatic proteins can either promote or inhibit angiogenesis, depending on the context and the specific protein involved. Some examples of angiostatic proteins include thrombospondin-1, endostatin, and angiostatin. Thrombospondin-1 is a large extracellular matrix protein that inhibits angiogenesis by binding to and blocking the activity of several pro-angiogenic growth factors, such as vascular endothelial growth factor (VEGF) and fibroblast growth factor (FGF). Endostatin is a fragment of collagen XVIII that inhibits angiogenesis by binding to and activating the receptor for VEGF, preventing it from binding to its target cells and promoting blood vessel growth. Angiostatin is a proteolytic fragment of plasminogen that inhibits angiogenesis by blocking the activity of several pro-angiogenic growth factors, including VEGF and basic fibroblast growth factor (bFGF). Overall, angiostatic proteins play a critical role in regulating blood vessel formation and are important targets for the development of anti-angiogenic therapies for various diseases, including cancer, cardiovascular disease, and age-related macular degeneration.
Neovascularization, pathologic, refers to the abnormal growth of new blood vessels in the body. This can occur in response to a variety of factors, including injury, inflammation, and certain diseases. In some cases, neovascularization can be a normal part of the healing process, but in other cases it can be a sign of a more serious underlying condition. Pathologic neovascularization is often associated with conditions such as cancer, diabetes, and age-related macular degeneration. It can also be seen in the development of certain types of tumors, where the new blood vessels help to provide the tumor with the nutrients and oxygen it needs to grow. Treatment for pathologic neovascularization may involve medications, laser therapy, or surgery, depending on the underlying cause and the severity of the condition.
Toll-like receptor 4 (TLR4) is a type of protein that plays a crucial role in the innate immune system. It is a member of the toll-like receptor family, which is a group of proteins that recognize and respond to pathogen-associated molecular patterns (PAMPs) on the surface of invading microorganisms. TLR4 is expressed on the surface of immune cells, such as macrophages and dendritic cells, as well as on non-immune cells, such as endothelial cells and fibroblasts. When TLR4 recognizes a PAMP, it triggers a signaling cascade that leads to the activation of immune cells and the production of pro-inflammatory cytokines and chemokines. TLR4 is also involved in the recognition of endogenous danger signals, such as those released by damaged or dying cells, and plays a role in the development of chronic inflammatory diseases, such as atherosclerosis, asthma, and inflammatory bowel disease. In the medical field, TLR4 is an important target for the development of new drugs and therapies for a variety of diseases, including infectious diseases, autoimmune disorders, and cancer.
Ovalbumin is a protein found in egg whites. It is a major allergen and can cause allergic reactions in some people. In the medical field, ovalbumin is often used as a model antigen for studying allergic reactions and for developing allergy vaccines. It is also used in research to study the structure and function of proteins, as well as in the production of various medical products, such as diagnostic reagents and pharmaceuticals.
A cell line, tumor is a type of cell culture that is derived from a cancerous tumor. These cell lines are grown in a laboratory setting and are used for research purposes, such as studying the biology of cancer and testing potential new treatments. They are typically immortalized, meaning that they can continue to divide and grow indefinitely, and they often exhibit the characteristics of the original tumor from which they were derived, such as specific genetic mutations or protein expression patterns. Cell lines, tumor are an important tool in cancer research and have been used to develop many of the treatments that are currently available for cancer patients.
Lymphotoxin-beta (LT-beta) is a cytokine that plays a role in the immune system. It is produced by activated T cells, B cells, and dendritic cells, and it has both pro-inflammatory and anti-inflammatory effects. In the context of the immune system, LT-beta is involved in the development and maintenance of lymphoid tissues, such as lymph nodes and spleen, and it plays a role in the regulation of immune cell trafficking. In the medical field, LT-beta has been studied for its potential therapeutic applications in the treatment of various diseases, including autoimmune disorders, cancer, and viral infections.
Pneumonia is a respiratory infection that affects the lungs. It is caused by bacteria, viruses, or fungi, and can be acute or chronic. Symptoms of pneumonia include cough, fever, chest pain, difficulty breathing, and fatigue. Pneumonia can be treated with antibiotics, antiviral medication, or antifungal medication, depending on the cause of the infection. In severe cases, hospitalization may be necessary.
Receptors, Interleukin-17 (IL-17R) are a type of protein receptor found on the surface of certain cells in the immune system. These receptors are responsible for binding to the cytokine Interleukin-17 (IL-17), which is produced by immune cells in response to infection or inflammation. IL-17 plays an important role in the immune response to infections, particularly by promoting the recruitment and activation of immune cells to the site of infection. IL-17R is expressed on a variety of immune cells, including neutrophils, macrophages, and T cells, and is thought to play a role in regulating the immune response to infection and inflammation. In the medical field, IL-17R is of interest as a potential target for the treatment of a variety of inflammatory and autoimmune diseases, such as rheumatoid arthritis, psoriasis, and inflammatory bowel disease. In these conditions, the overproduction of IL-17 can lead to chronic inflammation and tissue damage, and targeting IL-17R may help to reduce inflammation and improve symptoms.
Rheumatoid arthritis (RA) is a chronic autoimmune disorder that primarily affects the joints. It is characterized by inflammation and damage to the lining of the joint capsule, which leads to pain, stiffness, and reduced range of motion. RA can also affect other organs, such as the lungs, heart, and eyes. RA is a systemic disease, meaning that it affects the entire body, not just the joints. It is an inflammatory disease, meaning that it is caused by the immune system attacking healthy cells and tissues in the body. RA is a progressive disease, meaning that it can worsen over time if left untreated. However, with proper treatment, it is possible to manage the symptoms and slow down the progression of the disease. The exact cause of RA is not fully understood, but it is believed to be a combination of genetic and environmental factors. Risk factors for RA include being female, having a family history of the disease, and smoking.
Integrin alpha4beta1, also known as very late antigen-4 (VLA-4), is a cell surface protein that plays a crucial role in the adhesion and migration of immune cells, particularly leukocytes, to the endothelium of blood vessels. It is composed of two subunits, alpha4 and beta1, which are encoded by different genes. In the context of the immune system, integrin alpha4beta1 is involved in the homing of immune cells to specific tissues, such as the lymph nodes, spleen, and bone marrow. It also plays a role in the activation and differentiation of immune cells, as well as in the regulation of inflammation and immune responses. In addition to its role in the immune system, integrin alpha4beta1 has been implicated in various diseases, including cancer, autoimmune disorders, and infectious diseases. For example, it has been shown to be involved in the metastasis of certain types of cancer cells, as well as in the pathogenesis of multiple sclerosis and rheumatoid arthritis. Overall, integrin alpha4beta1 is a key regulator of immune cell function and has important implications for the development and treatment of various diseases.
Disease progression refers to the worsening or progression of a disease over time. It is a natural course of events that occurs in many chronic illnesses, such as cancer, heart disease, and diabetes. Disease progression can be measured in various ways, such as changes in symptoms, physical examination findings, laboratory test results, or imaging studies. In some cases, disease progression can be slowed or stopped through medical treatment, such as medications, surgery, or radiation therapy. However, in other cases, disease progression may be inevitable, and the focus of treatment may shift from trying to cure the disease to managing symptoms and improving quality of life. Understanding disease progression is important for healthcare providers to develop effective treatment plans and to communicate with patients about their condition and prognosis. It can also help patients and their families make informed decisions about their care and treatment options.
In the medical field, a base sequence refers to the specific order of nucleotides (adenine, thymine, cytosine, and guanine) that make up the genetic material (DNA or RNA) of an organism. The base sequence determines the genetic information encoded within the DNA molecule and ultimately determines the traits and characteristics of an individual. The base sequence can be analyzed using various techniques, such as DNA sequencing, to identify genetic variations or mutations that may be associated with certain diseases or conditions.
Interleukin-10 (IL-10) is a cytokine, which is a type of signaling molecule that plays a role in regulating the immune system. It is produced by various immune cells, including macrophages, dendritic cells, and T cells, in response to infection or inflammation. IL-10 has anti-inflammatory properties and helps to suppress the immune response, which can be beneficial in preventing excessive inflammation and tissue damage. It also has immunosuppressive effects, which can help to prevent autoimmune diseases and transplant rejection. In the medical field, IL-10 is being studied for its potential therapeutic applications in a variety of conditions, including inflammatory diseases, autoimmune diseases, and cancer. For example, IL-10 has been shown to be effective in reducing inflammation and improving symptoms in patients with rheumatoid arthritis, Crohn's disease, and other inflammatory conditions. It is also being investigated as a potential treatment for cancer, as it may help to suppress the immune response that allows cancer cells to evade detection and destruction by the immune system.
Cell proliferation refers to the process of cell division and growth, which is essential for the maintenance and repair of tissues in the body. In the medical field, cell proliferation is often studied in the context of cancer, where uncontrolled cell proliferation can lead to the formation of tumors and the spread of cancer cells to other parts of the body. In normal cells, cell proliferation is tightly regulated by a complex network of signaling pathways and feedback mechanisms that ensure that cells divide only when necessary and that they stop dividing when they have reached their full capacity. However, in cancer cells, these regulatory mechanisms can become disrupted, leading to uncontrolled cell proliferation and the formation of tumors. In addition to cancer, cell proliferation is also important in other medical conditions, such as wound healing, tissue regeneration, and the development of embryos. Understanding the mechanisms that regulate cell proliferation is therefore critical for developing new treatments for cancer and other diseases.
Toll-like receptor 2 (TLR2) is a type of protein that plays a crucial role in the innate immune system. It is a member of the Toll-like receptor family, which is a group of proteins that recognize and respond to pathogen-associated molecular patterns (PAMPs) on the surface of invading microorganisms. TLR2 is expressed on the surface of various immune cells, including macrophages, dendritic cells, and neutrophils. When it encounters a PAMP, such as lipoteichoic acid or peptidoglycan, it triggers a signaling cascade that leads to the activation of immune cells and the production of pro-inflammatory cytokines. TLR2 is also involved in the recognition of damage-associated molecular patterns (DAMPs), which are molecules that are released by damaged or dying cells. Activation of TLR2 by DAMPs can lead to the activation of immune cells and the initiation of an inflammatory response. In the medical field, TLR2 is being studied for its potential role in the development of new therapies for a variety of diseases, including infectious diseases, autoimmune disorders, and cancer. For example, TLR2 agonists are being investigated as potential treatments for bacterial infections, while TLR2 antagonists are being studied as potential therapies for autoimmune diseases and cancer.
Glycosaminoglycans (GAGs) are a group of complex carbohydrates that are found in the extracellular matrix of connective tissues in the human body. They are composed of repeating disaccharide units of a sugar called glucose and another sugar called uronic acid, which are linked together by glycosidic bonds. GAGs play important roles in various biological processes, including cell signaling, tissue development, and wound healing. They are also involved in the regulation of inflammation, blood clotting, and the immune response. In the medical field, GAGs are often studied in relation to various diseases and conditions, such as osteoarthritis, rheumatoid arthritis, and cancer. They are also used as diagnostic markers and therapeutic targets in the treatment of these conditions. Additionally, GAGs are used in various medical applications, such as wound dressings, tissue engineering, and drug delivery systems.
Asthma is a chronic respiratory disease characterized by inflammation and narrowing of the airways in the lungs. This can cause symptoms such as wheezing, coughing, shortness of breath, and chest tightness. Asthma can be triggered by a variety of factors, including allergens, irritants, exercise, and respiratory infections. It is a common condition, affecting millions of people worldwide, and can range from mild to severe. Treatment typically involves the use of medications to control inflammation and open up the airways, as well as lifestyle changes to avoid triggers and improve overall lung function.
In the medical field, an allergen is a substance that triggers an allergic reaction in a person. When a person with an allergy comes into contact with an allergen, their immune system reacts by producing antibodies called immunoglobulin E (IgE). These antibodies bind to cells in the body, causing them to release chemicals such as histamine, which can cause symptoms such as itching, swelling, and difficulty breathing. Allergens can be found in a wide range of substances, including foods, pollen, dust mites, pet dander, insect stings, and medications. Some common allergens include peanuts, tree nuts, shellfish, milk, eggs, wheat, soy, fish, and sesame seeds. Allergens can be inhaled, ingested, injected, or touched, and the severity of an allergic reaction can vary widely depending on the individual and the allergen. In severe cases, an allergic reaction can be life-threatening and require immediate medical attention.
Interleukin-4 (IL-4) is a type of cytokine, which is a signaling molecule that plays a crucial role in regulating the immune system. IL-4 is primarily produced by T-helper 2 (Th2) cells, which are a type of immune cell that helps to fight off parasitic infections and allergies. IL-4 has several important functions in the immune system. It promotes the differentiation of Th2 cells and stimulates the production of other Th2 cytokines, such as IL-5 and IL-13. IL-4 also promotes the activation and proliferation of B cells, which are responsible for producing antibodies. Additionally, IL-4 has anti-inflammatory effects and can help to suppress the activity of T-helper 1 (Th1) cells, which are involved in fighting off bacterial and viral infections. In the medical field, IL-4 is being studied for its potential therapeutic applications. For example, it is being investigated as a treatment for allergies, asthma, and certain autoimmune diseases. IL-4 is also being studied as a potential cancer immunotherapy, as it can help to activate immune cells that can recognize and attack cancer cells.
Astrocytes are a type of glial cell found in the central nervous system (CNS), including the brain and spinal cord. They are star-shaped cells that play a crucial role in supporting and maintaining the health of neurons, which are the nerve cells that transmit information throughout the brain and spinal cord. Astrocytes have many functions in the brain, including: 1. Providing structural support to neurons and synapses, the connections between neurons. 2. Regulating the extracellular environment by controlling the levels of ions, neurotransmitters, and other molecules in the brain. 3. Maintaining the blood-brain barrier, which protects the brain from harmful substances in the bloodstream. 4. Participating in the formation and repair of blood vessels in the brain. 5. Modulating the activity of neurons by releasing signaling molecules called gliotransmitters. Astrocytes are also involved in many neurological disorders, including Alzheimer's disease, multiple sclerosis, and epilepsy. Understanding the role of astrocytes in the brain is an active area of research in neuroscience and may lead to new treatments for these and other neurological conditions.
Interleukin-13 (IL-13) is a type of cytokine, which is a signaling molecule that plays a role in regulating the immune system. It is produced by various types of immune cells, including T cells, B cells, and mast cells, and is involved in the inflammatory response. IL-13 has a number of effects on the body, including: 1. Anti-inflammatory effects: IL-13 can reduce inflammation by inhibiting the production of pro-inflammatory cytokines and chemokines, and by promoting the production of anti-inflammatory cytokines. 2. Mucosal protection: IL-13 has been shown to protect the mucous membranes of the respiratory and gastrointestinal tracts, helping to prevent infections and maintain tissue integrity. 3. Fibrosis inhibition: IL-13 can inhibit the production of fibrotic tissue, which is the excessive accumulation of connective tissue that can lead to organ damage and scarring. 4. Allergy and asthma: IL-13 plays a key role in the development of allergic reactions and asthma, by promoting the production of IgE antibodies and by increasing the sensitivity of airways to allergens. Overall, IL-13 is an important mediator of the immune response and has a number of important functions in the body.
CD11b is a type of protein found on the surface of certain immune cells, such as neutrophils and monocytes. It is a member of the integrin family of proteins, which are involved in cell adhesion and signaling. CD11b is also known as the alpha chain of the integrin receptor Mac-1 (Macrophage-1 antigen). Antigens, CD11b are molecules that bind to CD11b on the surface of immune cells. These antigens can be foreign substances, such as bacteria or viruses, or they can be self-molecules that have been altered in some way. When CD11b binds to an antigen, it triggers a series of signaling events that activate the immune cell and cause it to respond to the presence of the antigen. This response can include the production of inflammatory molecules, the recruitment of other immune cells to the site of the antigen, and the destruction of the antigen. CD11b and its antigens play an important role in the immune response and are the subject of ongoing research in the field of immunology.
Interleukin-1alpha (IL-1α) is a type of cytokine, which is a signaling molecule that plays a crucial role in the immune system. It is produced by a variety of cells, including macrophages, monocytes, and dendritic cells, in response to infection, injury, or inflammation. IL-1α is involved in the regulation of immune responses, including the activation of T cells, B cells, and natural killer cells. It also plays a role in the production of other cytokines and chemokines, which help to recruit immune cells to the site of infection or injury. In addition to its role in the immune system, IL-1α has been implicated in a number of other physiological processes, including the regulation of bone metabolism, the control of blood pressure, and the regulation of pain perception. Abnormal levels of IL-1α have been associated with a number of medical conditions, including inflammatory diseases such as rheumatoid arthritis and psoriasis, as well as neurodegenerative diseases such as Alzheimer's and Parkinson's. As such, IL-1α is an important target for the development of new therapeutic strategies for these conditions.
Calcium is a chemical element with the symbol Ca and atomic number 20. It is a vital mineral for the human body and is essential for many bodily functions, including bone health, muscle function, nerve transmission, and blood clotting. In the medical field, calcium is often used to diagnose and treat conditions related to calcium deficiency or excess. For example, low levels of calcium in the blood (hypocalcemia) can cause muscle cramps, numbness, and tingling, while high levels (hypercalcemia) can lead to kidney stones, bone loss, and other complications. Calcium supplements are often prescribed to people who are at risk of developing calcium deficiency, such as older adults, vegetarians, and people with certain medical conditions. However, it is important to note that excessive calcium intake can also be harmful, and it is important to follow recommended dosages and consult with a healthcare provider before taking any supplements.
Toll-like receptor 3 (TLR3) is a type of protein that plays a crucial role in the innate immune system. It is a member of the Toll-like receptor family, which is a group of proteins that recognize and respond to pathogen-associated molecular patterns (PAMPs) on the surface of invading microorganisms. TLR3 is expressed on the surface of immune cells, including macrophages, dendritic cells, and epithelial cells, and is activated by double-stranded RNA (dsRNA), which is a common feature of viruses. When TLR3 detects dsRNA, it triggers a signaling cascade that leads to the production of pro-inflammatory cytokines and chemokines, as well as the activation of immune cells. TLR3 is also involved in the recognition of self-DNA and RNA, which can be released from damaged cells and trigger an inflammatory response in the absence of an infection. This process, known as sterile inflammation, has been implicated in the pathogenesis of several diseases, including autoimmune disorders, cancer, and neurodegenerative diseases. Overall, TLR3 plays a critical role in the recognition and response to viral infections and the regulation of immune responses to self-DNA and RNA.
Blotting, Western is a laboratory technique used to detect specific proteins in a sample by transferring proteins from a gel to a membrane and then incubating the membrane with a specific antibody that binds to the protein of interest. The antibody is then detected using an enzyme or fluorescent label, which produces a visible signal that can be quantified. This technique is commonly used in molecular biology and biochemistry to study protein expression, localization, and function. It is also used in medical research to diagnose diseases and monitor treatment responses.
Hypersensitivity is a medical term used to describe an exaggerated immune response to a substance that is normally harmless or even beneficial to the body. This response can occur in response to a variety of stimuli, including allergens, toxins, and medications. There are four main types of hypersensitivity reactions, each with its own specific characteristics and mechanisms: 1. Type I hypersensitivity (also known as immediate hypersensitivity) is an allergic reaction that occurs within minutes or hours of exposure to an allergen. It is mediated by IgE antibodies and involves the release of histamine and other inflammatory mediators from mast cells and basophils. 2. Type II hypersensitivity (also known as cytotoxic hypersensitivity) is an immune response that involves the destruction of cells by antibodies. It is typically seen in autoimmune diseases, where the immune system mistakenly attacks the body's own cells. 3. Type III hypersensitivity (also known as immune complex-mediated hypersensitivity) is an immune response that involves the formation of immune complexes, which can deposit in tissues and trigger inflammation. It is seen in conditions such as systemic lupus erythematosus and rheumatoid arthritis. 4. Type IV hypersensitivity (also known as delayed-type hypersensitivity) is an immune response that occurs over a period of days or weeks after exposure to an allergen or antigen. It involves the activation of T cells and the release of cytokines, which can cause inflammation and tissue damage. Overall, hypersensitivity reactions can range from mild to severe and can cause a wide range of symptoms, including itching, swelling, redness, and pain. Treatment typically involves avoiding the allergen or antigen that triggers the reaction, as well as medications to manage symptoms and reduce inflammation.
Membrane glycoproteins are proteins that are attached to the cell membrane through a glycosyl group, which is a complex carbohydrate. These proteins play important roles in cell signaling, cell adhesion, and cell recognition. They are involved in a wide range of biological processes, including immune response, cell growth and differentiation, and nerve transmission. Membrane glycoproteins can be classified into two main types: transmembrane glycoproteins, which span the entire cell membrane, and peripheral glycoproteins, which are located on one side of the membrane.
CC chemokine receptors
C-C chemokine receptor type 6
C-C chemokine receptor type 7
C-C motif chemokine ligand 27
C-C motif chemokine ligand 24
C-C motif chemokine ligand 3 like 3
Family with sequence similarity 19 (chemokine (C-C motif)-like), member A1
Family with sequence similarity 19 member A4, C-C motif chemokine like
CCL7
Eotaxin
CCR10
Chemotaxis
CCR2
Marco Baggiolini
Owais Mohammad
CCL5
CCL8
Chemokine
Role of microglia in disease
CCL11
Cédric Blanpain
CCL3
CCR4
CCL22
CXC chemokine receptors
CCL14
CCL19
CCL28
CCL25
CCRL1
CCL17
CCR3 (gene)
CC chemokine receptors - Wikipedia
Hematopoietic CC-chemokine receptor 2 (CCR2) competent cells are protective for the cognitive impairments and amyloid pathology...
Ccl21a, chemokine (C-C motif) ligand 21A (serine) - Creative BioMart
Chemokines, CC | DrugBank Online
Recombinant Human C-C Motif Chemokine 3-Like 1/CCL3L1 (C-6His) | Bon Opus Biosciences
Effector stage CC chemokine receptor-1 selective antagonism reduces multiple sclerosis-like rat disease | OffspringBiosciences
Ackr4 MGI Mouse Gene Detail - MGI:2181676 - atypical chemokine receptor 4
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Tissue Cell Type - CCL26 - The Human Protein Atlas
barium molecular entity - Ontology Report - Rat Genome Database
NIOSHTIC-2 Search Results - Full View
Frontiers | Pro-tumorigenic role of type 2 diabetes-induced cellular senescence in colorectal cancer
Researchers find subset of cardiac fibroblasts involved in cardiac inflammation under stress - King's College London
First Step to Creating HIV-Resistant T Cells in Patients (Transcript)
Long Coronavirus 2019 (COVID-19): Overview, Chronic COVID-19, Chronic Fatigue Syndrome/ Myalgic Encephalomyelitis
Recombinant Human Eotaxin-2 (CCL24)
Active Macrophage Inflammatory Protein 1 Beta (MIP1b) | APA093Hu02 | Cloud-Clone
BindingDB PrimarySearch ki
Idiopathic pulmonary fibrosis pathophysiology - wikidoc
Integrated Network Pharmacology and Mice Model to Investigate Qing Zao Fang for Treating Sjögren's Syndrome
KEGG PATHWAY: hsa05171
Post-transplant bronchiolitis obliterans | European Respiratory Society
Human CCL5 RANTES ELISA MAX Deluxe
Correlation between genetic polymorphism of angiopoietin-2 gene and clinical aspects of rheumatoid arthritis
Structural basis for ligand modulation of the CCR2 conformational landscape. - International Association for the Study of Pain ...
CCR11 (ACKR4) (NM 016557) Human Tagged ORF Clone - RC210172 | OriGene
Ligand5
- The specific ligand of this receptor is CCL25 To note, the chemokine binding protein D6 had previously been named CCR9, but this molecule is a scavenger receptor not a true (signaling) chemokine receptor. (wikipedia.org)
- However, due to the inability of this molecule (also known as CCRL1 and CCX CKR) to generate a signal following ligand interaction, it has been suggested that it is a scavenger receptor for chemokines and not a bona fide chemokine receptor. (wikipedia.org)
- Chemokine (C-C motif) ligand 21 (CCL21) is a small cytokine belonging to the CC chemokine family. (creativebiomart.net)
- It is known that C-C motif chemokine ligand 2 (CCL2) is a chemokine which facilitates monocyte movement and positioning. (kcl.ac.uk)
- The researchers analyzed the tear fluid collected for concentration of α synuclein, CC chemokine ligand 2 (CCL-2), and DJ-1 (Parkinson's disease protein 7). (medscape.com)
Receptors10
- CC chemokine receptors (or beta chemokine receptors) are integral membrane proteins that specifically bind and respond to cytokines of the CC chemokine family. (wikipedia.org)
- They represent one subfamily of chemokine receptors, a large family of G protein-linked receptors that are known as seven transmembrane (7-TM) proteins since they span the cell membrane seven times. (wikipedia.org)
- The CC chemokine receptors all work by activating the G protein Gi. (wikipedia.org)
- This molecule was originally designated CCR11 due to its ability to bind several CC chemokines (including CCL19, CCL21 and CCL25) and its structural similarity to chemokine receptors. (wikipedia.org)
- Several human chemokine receptors have been sons than for those homozygous for the wild classified as such on the basis of similarity of type CCR5 (12,17-19,23). (cdc.gov)
- What Are Chemokine Receptors? (cdc.gov)
- CC chemokines participate in the recruitment and activation of immune cells through CC chemokine receptors (CCRs). (elsevierpure.com)
- These class A G-protein coupled receptors (GPCRs) are involved in mammalian signaling pathways and control cell migration toward endogenous CC chemokine ligands, named for the adjacent cysteine motif on their N terminus. (iasp-pain.org)
- Chemokine receptors and their associated ligands are involved in a wide range of diseases and thus have become important drug targets. (iasp-pain.org)
- The integration of pathogen-associated molecular patterns (PAMPs) from microorganisms with their surface receptors in the immune cells, induces the production of several cytokines and chemokines that presents either a pro- and/or anti-inflammatory role by stimulating the secretion of a great variety of antibody subtypes and the activation of mechanisms of controlling the disease, such as the regulatory T cells. (bvsalud.org)
CCR55
- We describe the role of allelic polymorphism in the gene coding for the CCR5 chemokine receptor with regard to susceptibility to and disease course of HIV infection. (cdc.gov)
- SUMMARY A direct correlation between HIV infection and mutation in the chemokine receptor ( CCR5 ) gene has been established. (who.int)
- HIV-1 is influenced by a mutation in the 1 infection with a typical delay of 2-4 years chemokine receptor ( CCR5 ) gene [ 3,4 ]. (who.int)
- CCR5 (chemokine [C-C motif] receptor 5) is the major transmembrane protein that serves as coreceptor, with CD4, for HIV. (medscape.com)
- A Polymorphism in C-C Chemokine Receptor 5 (CCR5) Associates with Löfgren's Syndrome and Alters Receptor Expression as well as Functional Response. (cdc.gov)
Inflammatory5
- CCR1 was the first CC chemokine receptor identified and binds multiple inflammatory/inducible (see inducible gene) CC chemokines (including CCL4, CCL5, CCL6, CCL14, CCL15, CCL16 and CCL23). (wikipedia.org)
- CCR3 is a receptor for multiple inflammatory/inducible CC chemokines, including CCL11, CCL26, CCL7, CCL13, CCL15, CCL24 and CCL5 that attract eosinophils, and CCL28 that attracts B and T lymphocytes to mucosal tissues. (wikipedia.org)
- Viral macrophage inflammatory protein-II (vMIP) is a highly basic protein and human chemokine analog encoded by human herpesvirus-8. (drugbank.com)
- In contrast to decreased cell recruitment, key inflammatory chemokines were elevated in the lungs of ETOH-RSV mice. (cdc.gov)
- It mainly acts on biological processes such as inflammatory response, chemokine metabolic process, and immune response as well as pathways such as FoxO signaling pathway, Yersinia infection, HIF-1 signaling pathway, and TNF signaling pathway. (hindawi.com)
CCR12
- These are named CCR1 to CCR10 according to the IUIS/WHO Subcommittee on Chemokine Nomenclature. (wikipedia.org)
- We have studied the role of the chemokine receptor CCR1 during the effector stage of myelin oligodendrocyte glycoprotein-induced experimental autoimmune encephalomyelitis in DA rats. (offspringbiosciences.com)
Dendritic cells1
- Bouchon A, Hernandez-Munain C, Cella M, Colonna M. A DAP12-mediated pathway regulates expression of CC chemokine receptor 7 and maturation of human dendritic cells. (medlineplus.gov)
CCRL11
- Thus CCRL1 should not be called CCR11 under the guidelines of the IUIS/WHO Subcommittee on Chemokine Nomenclature. (wikipedia.org)
CCR22
- Here we show that these mechanisms specifically require CC-chemokine receptor 2 (CCR2) expression in bone marrow cells (BMCs). (nih.gov)
- CC chemokine receptor 2 (CCR2) is a part of the chemokine receptor family, an important class of therapeutic targets. (iasp-pain.org)
CCL212
- Its ligands include the related chemokines CCL19 and CCL21, (previously called ELC and SLC). (wikipedia.org)
- CCL21 elicits its effects by binding to a cell surface chemokine receptor known as CCR7. (creativebiomart.net)
Cysteine2
- This chemokine is also known as 6Ckine (because it has six conserved cysteine residues instead of the four cysteines typical to chemokines), exodus-2, and secondary lymphoid-tissue chemokine (SLC). (creativebiomart.net)
- Eotaxin-2 contains the four conserved cysteine residues present in CC chemokines. (peprotech.com)
CCL171
- The CC chemokines CCL3, CCL5, CCL17 and CCL22 signal through this receptor. (wikipedia.org)
Signaling pathway1
- We selected most pathways Ccl21a participated on our site, such as Cytokine-cytokine receptor interaction, Chemokine signaling pathway, NF-kappa B signaling pathway, which may be useful for your reference. (creativebiomart.net)
CXCL101
- Ectopic expressions of CXC chemokines (CXCL9, CXCL10, CXCL11, and CXCL13), interleukins (IL-1/2/4/6/10/12/17/22/23), IFN- γ, and TNF- α occur in the minor salivary glands of SS patients as compared to healthy individuals [ 10 , 11 ]. (hindawi.com)
CCL51
- CCL5, also known as RANTES, is a member of the CC family of chemokines. (biolegend.com)
CCR31
- Eotaxin-2 is a CC chemokine that signals through the CCR3 receptor. (peprotech.com)
Gene1
- Recombinant Human C-C Motif Chemokine 3-Like 1 is produced by our Mammalian expression system and the target gene encoding Ala24-Ala93 is expressed with a 6His tag at the C-terminus. (bonopusbio.com)
Infection1
- Lymphocyte recruitment was significantly reduced in the BAL 4 days after RSV infection in ETOH-RSV mice, whereas chemokine levels were the highest in this group at all experimental time points examined in comparison to RSV (p (cdc.gov)
Family1
- One major discovery was that members of the chemokine receptor family serve as cofactors for HIV entry into cells. (cdc.gov)
Type1
- Stimulation with SARS-CoV-2 spike protein or LPS triggered exaggerated prostanoid-, type I IFN-, and chemokine responses in post COVID-19 MDM. (nature.com)
Cell1
- Bronchoalveolar lavage (BAL) cell populations were measured by flow cytometry, and chemokines were detected by Western blot or ELISA. (cdc.gov)
Role1
- Before the discovery of the role of chemokine disease is expected to increase. (cdc.gov)
Memory1
- There is some suggestion that this chemokine receptor is restricted to memory T-cells within the lymphocyte pool. (wikipedia.org)
Members1
- To date, ten true members of the CC chemokine receptor subfamily have been described. (wikipedia.org)
Disease1
- Genetically engineered two-warhead evasins provide a method to achieve precision targeting of disease-relevant chemokine subsets. (peprotech.com)
Data1
- The data is made available under the Creative Commons License (CC BY 3.0, http://creativecommons.org/licenses/by/3.0/ ). (mcw.edu)