The lipid-rich sheath surrounding AXONS in both the CENTRAL NERVOUS SYSTEMS and PERIPHERAL NERVOUS SYSTEM. The myelin sheath is an electrical insulator and allows faster and more energetically efficient conduction of impulses. The sheath is formed by the cell membranes of glial cells (SCHWANN CELLS in the peripheral and OLIGODENDROGLIA in the central nervous system). Deterioration of the sheath in DEMYELINATING DISEASES is a serious clinical problem.
MYELIN-specific proteins that play a structural or regulatory role in the genesis and maintenance of the lamellar MYELIN SHEATH structure.
An abundant cytosolic protein that plays a critical role in the structure of multilamellar myelin. Myelin basic protein binds to the cytosolic sides of myelin cell membranes and causes a tight adhesion between opposing cell membranes.
A protein that accounts for more than half of the peripheral nervous system myelin protein. The extracellular domain of this protein is believed to engage in adhesive interactions and thus hold the myelin membrane compact. It can behave as a homophilic adhesion molecule through interactions with its extracellular domains. (From J Cell Biol 1994;126(4):1089-97)
A class of large neuroglial (macroglial) cells in the central nervous system. Oligodendroglia may be called interfascicular, perivascular, or perineuronal (not the same as SATELLITE CELLS, PERINEURONAL of GANGLIA) according to their location. They form the insulating MYELIN SHEATH of axons in the central nervous system.
Neuroglial cells of the peripheral nervous system which form the insulating myelin sheaths of peripheral axons.
A myelin protein that is the major component of the organic solvent extractable lipoprotein complexes of whole brain. It has been the subject of much study because of its unusual physical properties. It remains soluble in chloroform even after essentially all of its bound lipids have been removed. (From Siegel et al., Basic Neurochemistry, 4th ed, p122)
A class of nerve fibers as defined by their structure, specifically the nerve sheath arrangement. The AXONS of the myelinated nerve fibers are completely encased in a MYELIN SHEATH. They are fibers of relatively large and varied diameters. Their NEURAL CONDUCTION rates are faster than those of the unmyelinated nerve fibers (NERVE FIBERS, UNMYELINATED). Myelinated nerve fibers are present in somatic and autonomic nerves.
A nerve which originates in the lumbar and sacral spinal cord (L4 to S3) and supplies motor and sensory innervation to the lower extremity. The sciatic nerve, which is the main continuation of the sacral plexus, is the largest nerve in the body. It has two major branches, the TIBIAL NERVE and the PERONEAL NERVE.
Diseases characterized by loss or dysfunction of myelin in the central or peripheral nervous system.
Nerve fibers that are capable of rapidly conducting impulses away from the neuron cell body.
The nerves outside of the brain and spinal cord, including the autonomic, cranial, and spinal nerves. Peripheral nerves contain non-neuronal cells and connective tissue as well as axons. The connective tissue layers include, from the outside to the inside, the epineurium, the perineurium, and the endoneurium.
Regularly spaced gaps in the myelin sheaths of peripheral axons. Ranvier's nodes allow saltatory conduction, that is, jumping of impulses from node to node, which is faster and more energetically favorable than continuous conduction.
The main information-processing organs of the nervous system, consisting of the brain, spinal cord, and meninges.
Neoplasms which arise from nerve sheaths formed by SCHWANN CELLS in the PERIPHERAL NERVOUS SYSTEM or by OLIGODENDROCYTES in the CENTRAL NERVOUS SYSTEM. Malignant peripheral nerve sheath tumors, NEUROFIBROMA, and NEURILEMMOMA are relatively common tumors in this category.
A phosphodiesterase that specifically cleaves the 3'-phosphate linkage of 2',3'-cyclic nucleotides. It is found at high level in the cytoplasm of cells that form the MYELIN SHEATH.
A myelin protein found in the periaxonal membrane of both the central and peripheral nervous systems myelin sheaths. It binds to cells surface receptors found on AXONS and may regulate cellular interactions between MYELIN and AXONS.
Microscopy using an electron beam, instead of light, to visualize the sample, thereby allowing much greater magnification. The interactions of ELECTRONS with specimens are used to provide information about the fine structure of that specimen. In TRANSMISSION ELECTRON MICROSCOPY the reactions of the electrons that are transmitted through the specimen are imaged. In SCANNING ELECTRON MICROSCOPY an electron beam falls at a non-normal angle on the specimen and the image is derived from the reactions occurring above the plane of the specimen.
The 2nd cranial nerve which conveys visual information from the RETINA to the brain. The nerve carries the axons of the RETINAL GANGLION CELLS which sort at the OPTIC CHIASM and continue via the OPTIC TRACTS to the brain. The largest projection is to the lateral geniculate nuclei; other targets include the SUPERIOR COLLICULI and the SUPRACHIASMATIC NUCLEI. Though known as the second cranial nerve, it is considered part of the CENTRAL NERVOUS SYSTEM.
Degeneration of distal aspects of a nerve axon following injury to the cell body or proximal portion of the axon. The process is characterized by fragmentation of the axon and its MYELIN SHEATH.
A cylindrical column of tissue that lies within the vertebral canal. It is composed of WHITE MATTER and GRAY MATTER.
The outermost cytoplasmic layer of the SCHWANN CELLS covering NERVE FIBERS.
Renewal or physiological repair of damaged nerve tissue.
Myelin-deficient mutants which are from the inbred Tabby-Jimpy strain.
The propagation of the NERVE IMPULSE along the nerve away from the site of an excitation stimulus.
The nervous system outside of the brain and spinal cord. The peripheral nervous system has autonomic and somatic divisions. The autonomic nervous system includes the enteric, parasympathetic, and sympathetic subdivisions. The somatic nervous system includes the cranial and spinal nerves and their ganglia and the peripheral sensory receptors.
GLYCOSPHINGOLIPIDS with a sulfate group esterified to one of the sugar groups.
Catalyzes the final step in the galactocerebroside biosynthesis pathway.
A hereditary motor and sensory neuropathy transmitted most often as an autosomal dominant trait and characterized by progressive distal wasting and loss of reflexes in the muscles of the legs (and occasionally involving the arms). Onset is usually in the second to fourth decade of life. This condition has been divided into two subtypes, hereditary motor and sensory neuropathy (HMSN) types I and II. HMSN I is associated with abnormal nerve conduction velocities and nerve hypertrophy, features not seen in HMSN II. (Adams et al., Principles of Neurology, 6th ed, p1343)
Nucleoside-2',3'-cyclic phosphate nucleotidohydrolase. Enzymes that catalyze the hydrolysis of the 2'- or 3'- phosphate bonds of 2',3'-cyclic nucleotides. Also hydrolyzes nucleoside monophosphates. Includes EC 3.1.4.16 and EC 3.1.4.37. EC 3.1.4.-.
A branch of the tibial nerve which supplies sensory innervation to parts of the lower leg and foot.
Mice which carry mutant genes for neurologic defects or abnormalities.
An autoimmune disorder mainly affecting young adults and characterized by destruction of myelin in the central nervous system. Pathologic findings include multiple sharply demarcated areas of demyelination throughout the white matter of the central nervous system. Clinical manifestations include visual loss, extra-ocular movement disorders, paresthesias, loss of sensation, weakness, dysarthria, spasticity, ataxia, and bladder dysfunction. The usual pattern is one of recurrent attacks followed by partial recovery (see MULTIPLE SCLEROSIS, RELAPSING-REMITTING), but acute fulminating and chronic progressive forms (see MULTIPLE SCLEROSIS, CHRONIC PROGRESSIVE) also occur. (Adams et al., Principles of Neurology, 6th ed, p903)
Electron microscopy in which the ELECTRONS or their reaction products that pass down through the specimen are imaged below the plane of the specimen.
An early growth response transcription factor that controls the formation of the MYELIN SHEATH around peripheral AXONS by SCHWANN CELLS. Mutations in EGR2 transcription factor have been associated with HEREDITARY MOTOR AND SENSORY NEUROPATHIES such as CHARCOT-MARIE-TOOTH DISEASE.
Loss of functional activity and trophic degeneration of nerve axons and their terminal arborizations following the destruction of their cells of origin or interruption of their continuity with these cells. The pathology is characteristic of neurodegenerative diseases. Often the process of nerve degeneration is studied in research on neuroanatomical localization and correlation of the neurophysiology of neural pathways.
The non-neuronal cells of the nervous system. They not only provide physical support, but also respond to injury, regulate the ionic and chemical composition of the extracellular milieu, participate in the BLOOD-BRAIN BARRIER and BLOOD-RETINAL BARRIER, form the myelin insulation of nervous pathways, guide neuronal migration during development, and exchange metabolites with neurons. Neuroglia have high-affinity transmitter uptake systems, voltage-dependent and transmitter-gated ion channels, and can release transmitters, but their role in signaling (as in many other functions) is unclear.
The part of CENTRAL NERVOUS SYSTEM that is contained within the skull (CRANIUM). Arising from the NEURAL TUBE, the embryonic brain is comprised of three major parts including PROSENCEPHALON (the forebrain); MESENCEPHALON (the midbrain); and RHOMBENCEPHALON (the hindbrain). The developed brain consists of CEREBRUM; CEREBELLUM; and other structures in the BRAIN STEM.
A transmembrane protein present in the MYELIN SHEATH of the CENTRAL NERVOUS SYSTEM. It is one of the main autoantigens implicated in the pathogenesis of MULTIPLE SCLEROSIS.
Neutral glycosphingolipids that contain a monosaccharide, normally glucose or galactose, in 1-ortho-beta-glycosidic linkage with the primary alcohol of an N-acyl sphingoid (ceramide). In plants the monosaccharide is normally glucose and the sphingoid usually phytosphingosine. In animals, the monosaccharide is usually galactose, though this may vary with the tissue and the sphingoid is usually sphingosine or dihydrosphingosine. (From Oxford Dictionary of Biochemistry and Molecular Biology, 1st ed)
An experimental animal model for central nervous system demyelinating disease. Inoculation with a white matter emulsion combined with FREUND'S ADJUVANT, myelin basic protein, or purified central myelin triggers a T cell-mediated immune response directed towards central myelin. The pathologic features are similar to MULTIPLE SCLEROSIS, including perivascular and periventricular foci of inflammation and demyelination. Subpial demyelination underlying meningeal infiltrations also occurs, which is also a feature of ENCEPHALOMYELITIS, ACUTE DISSEMINATED. Passive immunization with T-cells from an afflicted animal to a normal animal also induces this condition. (From Immunol Res 1998;17(1-2):217-27; Raine CS, Textbook of Neuropathology, 2nd ed, p604-5)
Methods of preparing tissue for examination and study of the origin, structure, function, or pathology.
A group of slowly progressive inherited disorders affecting motor and sensory peripheral nerves. Subtypes include HMSNs I-VII. HMSN I and II both refer to CHARCOT-MARIE-TOOTH DISEASE. HMSN III refers to hypertrophic neuropathy of infancy. HMSN IV refers to REFSUM DISEASE. HMSN V refers to a condition marked by a hereditary motor and sensory neuropathy associated with spastic paraplegia (see SPASTIC PARAPLEGIA, HEREDITARY). HMSN VI refers to HMSN associated with an inherited optic atrophy (OPTIC ATROPHIES, HEREDITARY), and HMSN VII refers to HMSN associated with retinitis pigmentosa. (From Adams et al., Principles of Neurology, 6th ed, p1343)
Paired bundles of NERVE FIBERS entering and leaving the SPINAL CORD at each segment. The dorsal and ventral nerve roots join to form the mixed segmental spinal nerves. The dorsal roots are generally afferent, formed by the central projections of the spinal (dorsal root) ganglia sensory cells, and the ventral roots are efferent, comprising the axons of spinal motor and PREGANGLIONIC AUTONOMIC FIBERS.
A peptide factor originally identified by its ability to stimulate the phosphorylation the erbB-2 receptor (RECEPTOR, ERBB-2). It is a ligand for the erbB-3 receptor (RECEPTOR, ERBB-3) and the erbB-4 receptor. Variant forms of NEUREGULIN-1 occur through alternative splicing of its mRNA.
Diseases of the peripheral nerves external to the brain and spinal cord, which includes diseases of the nerve roots, ganglia, plexi, autonomic nerves, sensory nerves, and motor nerves.
'Nerve tissue proteins' are specialized proteins found within the nervous system's biological tissue, including neurofilaments, neuronal cytoskeletal proteins, and neural cell adhesion molecules, which facilitate structural support, intracellular communication, and synaptic connectivity essential for proper neurological function.
Refers to animals in the period of time just after birth.
Sensory ganglia located on the dorsal spinal roots within the vertebral column. The spinal ganglion cells are pseudounipolar. The single primary branch bifurcates sending a peripheral process to carry sensory information from the periphery and a central branch which relays that information to the spinal cord or brain.
The use of statistical and mathematical methods to analyze biological observations and phenomena.
Strains of mice in which certain GENES of their GENOMES have been disrupted, or "knocked-out". To produce knockouts, using RECOMBINANT DNA technology, the normal DNA sequence of the gene being studied is altered to prevent synthesis of a normal gene product. Cloned cells in which this DNA alteration is successful are then injected into mouse EMBRYOS to produce chimeric mice. The chimeric mice are then bred to yield a strain in which all the cells of the mouse contain the disrupted gene. Knockout mice are used as EXPERIMENTAL ANIMAL MODELS for diseases (DISEASE MODELS, ANIMAL) and to clarify the functions of the genes.
Slender processes of NEURONS, including the AXONS and their glial envelopes (MYELIN SHEATH). Nerve fibers conduct nerve impulses to and from the CENTRAL NERVOUS SYSTEM.
Broad plate of dense myelinated fibers that reciprocally interconnect regions of the cortex in all lobes with corresponding regions of the opposite hemisphere. The corpus callosum is located deep in the longitudinal fissure.
Histochemical localization of immunoreactive substances using labeled antibodies as reagents.
Changes in the amounts of various chemicals (neurotransmitters, receptors, enzymes, and other metabolites) specific to the area of the central nervous system contained within the head. These are monitored over time, during sensory stimulation, or under different disease states.
Type III intermediate filament proteins that assemble into neurofilaments, the major cytoskeletal element in nerve axons and dendrites. They consist of three distinct polypeptides, the neurofilament triplet. Types I, II, and IV intermediate filament proteins form other cytoskeletal elements such as keratins and lamins. It appears that the metabolism of neurofilaments is disturbed in Alzheimer's disease, as indicated by the presence of neurofilament epitopes in the neurofibrillary tangles, as well as by the severe reduction of the expression of the gene for the light neurofilament subunit of the neurofilament triplet in brains of Alzheimer's patients. (Can J Neurol Sci 1990 Aug;17(3):302)
Cerebrosides which contain as their polar head group a galactose moiety bound in glycosidic linkage to the hydroxyl group of ceramide. Their accumulation in tissue, due to a defect in beta-galactosidase, is the cause of galactosylceramide lipidosis or globoid cell leukodystrophy.
Laboratory mice that have been produced from a genetically manipulated EGG or EMBRYO, MAMMALIAN.
Cells propagated in vitro in special media conducive to their growth. Cultured cells are used to study developmental, morphologic, metabolic, physiologic, and genetic processes, among others.
Naturally occurring or experimentally induced animal diseases with pathological processes sufficiently similar to those of human diseases. They are used as study models for human diseases.
Descriptions of specific amino acid, carbohydrate, or nucleotide sequences which have appeared in the published literature and/or are deposited in and maintained by databanks such as GENBANK, European Molecular Biology Laboratory (EMBL), National Biomedical Research Foundation (NBRF), or other sequence repositories.
Microscopy in which the samples are first stained immunocytochemically and then examined using an electron microscope. Immunoelectron microscopy is used extensively in diagnostic virology as part of very sensitive immunoassays.
Inbred C57BL mice are a strain of laboratory mice that have been produced by many generations of brother-sister matings, resulting in a high degree of genetic uniformity and homozygosity, making them widely used for biomedical research, including studies on genetics, immunology, cancer, and neuroscience.
A class of large neuroglial (macroglial) cells in the central nervous system - the largest and most numerous neuroglial cells in the brain and spinal cord. Astrocytes (from "star" cells) are irregularly shaped with many long processes, including those with "end feet" which form the glial (limiting) membrane and directly and indirectly contribute to the BLOOD-BRAIN BARRIER. They regulate the extracellular ionic and chemical environment, and "reactive astrocytes" (along with MICROGLIA) respond to injury.
Surface ligands that mediate cell-to-cell adhesion and function in the assembly and interconnection of the vertebrate nervous system. These molecules promote cell adhesion via a homophilic mechanism. These are not to be confused with NEURAL CELL ADHESION MOLECULES, now known to be expressed in a variety of tissues and cell types in addition to nervous tissue.
Progressive restriction of the developmental potential and increasing specialization of function that leads to the formation of specialized cells, tissues, and organs.
Neoplasms which arise from peripheral nerve tissue. This includes NEUROFIBROMAS; SCHWANNOMAS; GRANULAR CELL TUMORS; and malignant peripheral NERVE SHEATH NEOPLASMS. (From DeVita Jr et al., Cancer: Principles and Practice of Oncology, 5th ed, pp1750-1)
A long flat muscle that extends along the whole length of both sides of the abdomen. It flexes the vertebral column, particularly the lumbar portion; it also tenses the anterior abdominal wall and assists in compressing the abdominal contents. It is frequently the site of hematomas. In reconstructive surgery it is often used for the creation of myocutaneous flaps. (From Gray's Anatomy, 30th American ed, p491)
The basic cellular units of nervous tissue. Each neuron consists of a body, an axon, and dendrites. Their purpose is to receive, conduct, and transmit impulses in the NERVOUS SYSTEM.
The part of brain that lies behind the BRAIN STEM in the posterior base of skull (CRANIAL FOSSA, POSTERIOR). It is also known as the "little brain" with convolutions similar to those of CEREBRAL CORTEX, inner white matter, and deep cerebellar nuclei. Its function is to coordinate voluntary movements, maintain balance, and learn motor skills.
The order of amino acids as they occur in a polypeptide chain. This is referred to as the primary structure of proteins. It is of fundamental importance in determining PROTEIN CONFORMATION.
Elements of limited time intervals, contributing to particular results or situations.
A moderately firm, benign, encapsulated tumor resulting from proliferation of SCHWANN CELLS and FIBROBLASTS that includes portions of nerve fibers. The tumors usually develop along peripheral or cranial nerves and are a central feature of NEUROFIBROMATOSIS 1, where they may occur intracranially or involve spinal roots. Pathologic features include fusiform enlargement of the involved nerve. Microscopic examination reveals a disorganized and loose cellular pattern with elongated nuclei intermixed with fibrous strands. (From Adams et al., Principles of Neurology, 6th ed, p1016)
A strain of albino rat used widely for experimental purposes because of its calmness and ease of handling. It was developed by the Sprague-Dawley Animal Company.
Test for tissue antigen using either a direct method, by conjugation of antibody with fluorescent dye (FLUORESCENT ANTIBODY TECHNIQUE, DIRECT) or an indirect method, by formation of antigen-antibody complex which is then labeled with fluorescein-conjugated anti-immunoglobulin antibody (FLUORESCENT ANTIBODY TECHNIQUE, INDIRECT). The tissue is then examined by fluorescence microscopy.
The posterior filiform portion of the spermatozoon (SPERMATOZOA) that provides sperm motility.
A technique of culturing mixed cell types in vitro to allow their synergistic or antagonistic interactions, such as on CELL DIFFERENTIATION or APOPTOSIS. Coculture can be of different types of cells, tissues, or organs from normal or disease states.
The gradual irreversible changes in structure and function of an organism that occur as a result of the passage of time.

Prior exposure to neurotrophins blocks inhibition of axonal regeneration by MAG and myelin via a cAMP-dependent mechanism. (1/2525)

MAG is a potent inhibitor of axonal regeneration. Here, inhibition by MAG, and myelin in general, is blocked if neurons are exposed to neurotrophins before encountering the inhibitor; priming cerebellar neurons with BDNF or GDNF, but not NGF, or priming DRG neurons with any of these neurotrophins blocks inhibition by MAG/myelin. Dibutyryl cAMP also overcomes inhibition by MAG/myelin, and cAMP is elevated by neurotrophins. A PKA inhibitor present during priming abrogates the block of inhibition. Finally, if neurons are exposed to MAG/myelin and neurotrophins simultaneously, but with the Gi protein inhibitor, inhibition is blocked. We suggest that priming neurons with particular neurotrophins elevates cAMP and activates PKA, which blocks subsequent inhibition of regeneration and that priming is required because MAG/myelin activates a Gi protein, which blocks increases in cAMP. This is important for encouraging axons to regrow in vivo.  (+info)

Disproportionate recruitment of CD8+ T cells into the central nervous system by professional antigen-presenting cells. (2/2525)

Inappropriate immune responses, thought to exacerbate or even to initiate several types of central nervous system (CNS) neuropathology, could arise from failures by either the CNS or the immune system. The extent that the inappropriate appearance of antigen-presenting cell (APC) function contributes to CNS inflammation and pathology is still under debate. Therefore, we characterized the response initiated when professional APCs (dendritic cells) presenting non-CNS antigens were injected into the CNS. These dendritic cells expressed numerous T-cell chemokines, but only in the presence of antigen did leukocytes accumulate in the ventricles, meninges, sub-arachnoid spaces, and injection site. Within the CNS parenchyma, the injected dendritic cells migrated preferentially into the white matter tracts, yet only a small percentage of the recruited leukocytes entered the CNS parenchyma, and then only in the white matter tracts. Although T-cell recruitment was antigen specific and thus mediated by CD4+ T cells in the models used here, CD8+ T cells accumulated in numbers equal to or greater than that of CD4+ T cells. Few of the recruited T cells expressed activation markers (CD25 and VLA-4), and those that did were primarily in the meninges, injection site, ventricles, and perivascular spaces but not in the parenchyma. These results indicate that 1) the CNS modulates the cellular composition and activation states of responding T-cell populations and that 2) myelin-restricted inflammation need not be initiated by a myelin-specific antigen.  (+info)

A new X linked neurodegenerative syndrome with mental retardation, blindness, convulsions, spasticity, mild hypomyelination, and early death maps to the pericentromeric region. (3/2525)

We report on a family with an X linked neurodegenerative disorder consisting of mental retardation, blindness, convulsions, spasticity, and early death. Neuropathological examination showed mild hypomyelination. By linkage analysis, the underlying genetic defect could be assigned to the pericentromeric region of the X chromosome with a maximum lod score of 3.30 at theta=0.0 for the DXS1204 locus with DXS337 and PGK1P1 as flanking markers.  (+info)

Myelin and collapsin-1 induce motor neuron growth cone collapse through different pathways: inhibition of collapse by opposing mutants of rac1. (4/2525)

Precise growth cone guidance is the consequence of a continuous reorganization of actin filament structures within filopodia and lamellipodia in response to inhibitory and promoting cues. The small GTPases rac1, cdc42, and rhoA are critical for regulating distinct actin structures in non-neuronal cells and presumably in growth cones. Collapse, a retraction of filopodia and lamellipodia, is a typical growth cone behavior on contact with inhibitory cues and is associated with depolymerization and redistribution of actin filaments. We examined whether small GTPases mediate the inhibitory properties of CNS myelin or collapsin-1, a soluble semaphorin, in chick embryonic motor neuron cultures. As demonstrated for collapsin-1, CNS myelin-evoked growth cone collapse was accompanied by a reduction of rhodamine-phalloidin staining most prominent in the growth cone periphery, suggesting actin filament disassembly. Specific mutants of small GTPases were capable of desensitizing growth cones to CNS myelin or collapsin-1. Adenoviral-mediated expression of constitutively active rac1 or rhoA abolished CNS myelin-induced collapse and allowed remarkable neurite extension on a CNS myelin substrate. In contrast, expression of dominant negative rac1 or cdc42 negated collapsin-1-induced growth cone collapse and promoted neurite outgrowth on a collapsin-1 substrate. These findings suggest that small GTPases can modulate the signaling pathways of inhibitory stimuli and, consequently, allow the manipulation of growth cone behavior. However, the fact that opposite mutants of rac1 were effective against different inhibitory stimuli speaks against a universal signaling pathway underlying growth cone collapse.  (+info)

Structural maturation of neural pathways in children and adolescents: in vivo study. (5/2525)

Structural maturation of fiber tracts in the human brain, including an increase in the diameter and myelination of axons, may play a role in cognitive development during childhood and adolescence. A computational analysis of structural magnetic resonance images obtained in 111 children and adolescents revealed age-related increases in white matter density in fiber tracts constituting putative corticospinal and frontotemporal pathways. The maturation of the corticospinal tract was bilateral, whereas that of the frontotemporal pathway was found predominantly in the left (speech-dominant) hemisphere. These findings provide evidence for a gradual maturation, during late childhood and adolescence, of fiber pathways presumably supporting motor and speech functions.  (+info)

Rapid induction of functional and morphological continuity between severed ends of mammalian or earthworm myelinated axons. (6/2525)

The inability to rapidly restore the loss of function that results from severance (cutting or crushing) of PNS and CNS axons is a severe clinical problem. As a novel strategy to help alleviate this problem, we have developed in vitro procedures using Ca2+-free solutions of polyethylene glycol (PEG solutions), which within minutes induce functional and morphological continuity (PEG-induced fusion) between the cut or crushed ends of myelinated sciatic or spinal axons in rats. Using a PEG-based hydrogel that binds to connective tissue to provide mechanical strength at the lesion site and is nontoxic to nerve tissues in earthworms and mammals, we have also developed in vivo procedures that permanently maintain earthworm myelinated medial giant axons whose functional and morphological integrity has been restored by PEG-induced fusion after axonal severance. In all these in vitro or in vivo procedures, the success of PEG-induced fusion of sciatic or spinal axons and myelinated medial giant axons is measured by the restored conduction of action potentials through the lesion site, the presence of intact axonal profiles in electron micrographs taken at the lesion site, and/or the intra-axonal diffusion of fluorescent dyes across the lesion site. These and other data suggest that the application of polymeric fusiogens (such as our PEG solutions), possibly combined with a tissue adherent (such as our PEG hydrogels), could lead to in vivo treatments that rapidly and permanently repair cut or crushed axons in the PNS and CNS of adult mammals, including humans.  (+info)

Synthesis and turnover of cerebrosides and phosphatidylserine of myelin and microsomal fractions of adult and developing rat brain. (7/2525)

The synthesis and turnover of cerebrosides and phospholipids was followed in microsomal and myelin fractions of developing and adult rat brains after an intracerebral injection of [U-14C]serine. The kinetics of incorporation of radioactivity into microsomal and myelin cerebrosides indicate the possibility of a precursor-product relationship between cerebrosides of these membranes. The specific radioactivity of myelin cerebrosides was corrected for the deposition of newly formed cerebrosides in myelin. Multiphasic curves were obtained for the decline in specific radioactivity of myelin and microsomal cerebrosides, suggesting different cerebroside pools in these membranes. The half-life of the fast turning-over pool of cerebrosides of myelin was 7 and 22 days for the developing and adult rat brain respectively. The half-life of the slowly turning-over pool of myelin cerebrosides was about 145 days for both groups of animals. The half-life of the rapidly turning-over microsomal cerebrosides was calculated to be 20 and 40 h for the developing and adult animals respectively. The half-life of the intermediate and slowly turning-over microsomal cerebrosides was 11 and 60 days respectively, for both groups of animals. The amount of incorporation of radioactivity into microsomal cerebrosides from L-serine was greatly decreased in the adult animals, and greater amounts of the precursor were directed towards the synthesis of phosphatidylserine. In the developing animals, considerable amounts of cerebrosides were synthesized from L-serine, besides phosphatidylserine. The time-course of incorporation indicated that a precursor-product relationship exists between microsomal and myelin phosphatidylserine. The half-life of microsomal phosphatidylserine was calculated to be about 8 h for the fast turning-over pool in both groups of animals.  (+info)

Adult brain retains the potential to generate oligodendroglial progenitors with extensive myelination capacity. (8/2525)

Remyelination of focal areas of the central nervous system (CNS) in animals can be achieved by transplantation of glial cells, yet the source of these cells in humans to similarly treat myelin disorders is limited at present to fetal tissue. Multipotent precursor cells are present in the CNS of adult as well as embryonic and neonatal animals and can differentiate into lineage-restricted progenitors such as oligodendroglial progenitors (OPs). The OPs present in adults have a different phenotype from those seen in earlier life, and their potential role in CNS repair remains unknown. To gain insights into the potential to manipulate the myelinating capacity of these precursor and/or progenitor cells, we generated a homogenous culture of OPs from neural precursor cells isolated from adult rat subependymal tissues. Phenotypic characterization indicated that these OPs resembled neonatal rather than adult OPs and produced robust myelin after transplantation. The ability to generate such cells from the adult brain therefore opens an avenue to explore the potential of these cells for repairing myelin disorders in adulthood.  (+info)

The myelin sheath is a multilayered, fatty substance that surrounds and insulates many nerve fibers in the nervous system. It is essential for the rapid transmission of electrical signals, or nerve impulses, along these nerve fibers, allowing for efficient communication between different parts of the body. The myelin sheath is produced by specialized cells called oligodendrocytes in the central nervous system (CNS) and Schwann cells in the peripheral nervous system (PNS). Damage to the myelin sheath, as seen in conditions like multiple sclerosis, can significantly impair nerve function and result in various neurological symptoms.

Myelin proteins are proteins that are found in the myelin sheath, which is a fatty (lipid-rich) substance that surrounds and insulates nerve fibers (axons) in the nervous system. The myelin sheath enables the rapid transmission of electrical signals (nerve impulses) along the axons, allowing for efficient communication between different parts of the nervous system.

There are several types of myelin proteins, including:

1. Proteolipid protein (PLP): This is the most abundant protein in the myelin sheath and plays a crucial role in maintaining the structure and function of the myelin sheath.
2. Myelin basic protein (MBP): This protein is also found in the myelin sheath and helps to stabilize the compact structure of the myelin sheath.
3. Myelin-associated glycoprotein (MAG): This protein is involved in the adhesion of the myelin sheath to the axon and helps to maintain the integrity of the myelin sheath.
4. 2'3'-cyclic nucleotide 3' phosphodiesterase (CNP): This protein is found in oligodendrocytes, which are the cells that produce the myelin sheath in the central nervous system. CNP plays a role in maintaining the structure and function of the oligodendrocytes.

Damage to myelin proteins can lead to demyelination, which is a characteristic feature of several neurological disorders, including multiple sclerosis (MS), Guillain-Barré syndrome, and Charcot-Marie-Tooth disease.

Myelin Basic Protein (MBP) is a key structural protein found in the myelin sheath, which is a multilayered membrane that surrounds and insulates nerve fibers (axons) in the nervous system. The myelin sheath enables efficient and rapid transmission of electrical signals (nerve impulses) along the axons, allowing for proper communication between different neurons.

MBP is one of several proteins responsible for maintaining the structural integrity and organization of the myelin sheath. It is a basic protein, meaning it has a high isoelectric point due to its abundance of positively charged amino acids. MBP is primarily located in the intraperiod line of the compact myelin, which is a region where the extracellular leaflets of the apposing membranes come into close contact without fusing.

MBP plays crucial roles in the formation, maintenance, and repair of the myelin sheath:

1. During development, MBP helps mediate the compaction of the myelin sheath by interacting with other proteins and lipids in the membrane.
2. MBP contributes to the stability and resilience of the myelin sheath by forming strong ionic bonds with negatively charged phospholipids in the membrane.
3. In response to injury or disease, MBP can be cleaved into smaller peptides that act as chemoattractants for immune cells, initiating the process of remyelination and repair.

Dysregulation or damage to MBP has been implicated in several demyelinating diseases, such as multiple sclerosis (MS), where the immune system mistakenly attacks the myelin sheath, leading to its degradation and loss. The presence of autoantibodies against MBP is a common feature in MS patients, suggesting that an abnormal immune response to this protein may contribute to the pathogenesis of the disease.

Myelin P0 protein, also known as P0 or MPZ (myelin protein zero), is a major structural component of the myelin sheath in the peripheral nervous system. The myelin sheath is a multilayered membrane that surrounds and insulates nerve fibers to increase the speed of electrical impulse transmission.

P0 protein is a transmembrane glycoprotein, which means it spans the lipid bilayer of the myelin membrane and has sugar molecules (glycans) attached to it. It plays a crucial role in maintaining the compact structure of the myelin sheath by forming homodimers that interact with each other through their extracellular domains, creating tight junctions between the apposing layers of the myelin membrane.

P0 protein also contributes to the stability and integrity of the myelin sheath by interacting with other myelin proteins, such as connexin 32 and peripheral myelin protein 22 (PMP22). Mutations in the MPZ gene can lead to various peripheral neuropathies, including Charcot-Marie-Tooth disease type 1B and Dejerine-Sottas syndrome.

Oligodendroglia are a type of neuroglial cell found in the central nervous system (CNS) of vertebrates, including humans. These cells play a crucial role in providing support and insulation to nerve fibers (axons) in the CNS, which includes the brain and spinal cord.

More specifically, oligodendroglia produce a fatty substance called myelin that wraps around axons, forming myelin sheaths. This myelination process helps to increase the speed of electrical impulse transmission (nerve impulses) along the axons, allowing for efficient communication between different neurons.

In addition to their role in myelination, oligodendroglia also contribute to the overall health and maintenance of the CNS by providing essential nutrients and supporting factors to neurons. Dysfunction or damage to oligodendroglia has been implicated in various neurological disorders, such as multiple sclerosis (MS), where demyelination of axons leads to impaired nerve function and neurodegeneration.

Schwann cells, also known as neurolemmocytes, are a type of glial cell that form the myelin sheath around peripheral nervous system (PNS) axons, allowing for the rapid and efficient transmission of nerve impulses. These cells play a crucial role in the maintenance and function of the PNS.

Schwann cells originate from the neural crest during embryonic development and migrate to the developing nerves. They wrap around the axons in a spiral fashion, forming multiple layers of myelin, which insulates the nerve fibers and increases the speed of electrical impulse transmission. Each Schwann cell is responsible for myelinating a single segment of an axon, with the gaps between these segments called nodes of Ranvier.

Schwann cells also provide structural support to the neurons and contribute to the regeneration of injured peripheral nerves by helping to guide the regrowth of axons to their targets. Additionally, Schwann cells can participate in immune responses within the PNS, such as releasing cytokines and chemokines to recruit immune cells during injury or infection.

Myelin Proteolipid Protein (PLP) is a major component of the myelin sheath, which is a fatty insulating substance that covers and protects nerve fibers in the central nervous system (CNS). PLP makes up about 50% of the proteins found in the myelin sheath. It plays a crucial role in the structure and function of the myelin sheath, including maintaining its compactness and stability. Defects or mutations in the gene that encodes for PLP can lead to various demyelinating diseases, such as X-linked adrenoleukodystrophy (X-ALD) and Pelizaeus-Merzbacher disease (PMD), which are characterized by the degeneration of the myelin sheath and subsequent neurological impairments.

Myelinated nerve fibers are neuronal processes that are surrounded by a myelin sheath, a fatty insulating substance that is produced by Schwann cells in the peripheral nervous system and oligodendrocytes in the central nervous system. This myelin sheath helps to increase the speed of electrical impulse transmission, also known as action potentials, along the nerve fiber. The myelin sheath has gaps called nodes of Ranvier where the electrical impulses can jump from one node to the next, which also contributes to the rapid conduction of signals. Myelinated nerve fibers are typically found in the peripheral nerves and the optic nerve, but not in the central nervous system (CNS) tracts that are located within the brain and spinal cord.

The sciatic nerve is the largest and longest nerve in the human body, running from the lower back through the buttocks and down the legs to the feet. It is formed by the union of the ventral rami (branches) of the L4 to S3 spinal nerves. The sciatic nerve provides motor and sensory innervation to various muscles and skin areas in the lower limbs, including the hamstrings, calf muscles, and the sole of the foot. Sciatic nerve disorders or injuries can result in symptoms such as pain, numbness, tingling, or weakness in the lower back, hips, legs, and feet, known as sciatica.

Demyelinating diseases are a group of disorders that are characterized by damage to the myelin sheath, which is the protective covering surrounding nerve fibers in the brain, optic nerves, and spinal cord. Myelin is essential for the rapid transmission of nerve impulses, and its damage results in disrupted communication between the brain and other parts of the body.

The most common demyelinating disease is multiple sclerosis (MS), where the immune system mistakenly attacks the myelin sheath. Other demyelinating diseases include:

1. Acute Disseminated Encephalomyelitis (ADEM): An autoimmune disorder that typically follows a viral infection or vaccination, causing widespread inflammation and demyelination in the brain and spinal cord.
2. Neuromyelitis Optica (NMO) or Devic's Disease: A rare autoimmune disorder that primarily affects the optic nerves and spinal cord, leading to severe vision loss and motor disability.
3. Transverse Myelitis: Inflammation of the spinal cord causing damage to both sides of one level (segment) of the spinal cord, resulting in various neurological symptoms such as muscle weakness, numbness, or pain, depending on which part of the spinal cord is affected.
4. Guillain-Barré Syndrome: An autoimmune disorder that causes rapid-onset muscle weakness, often beginning in the legs and spreading to the upper body, including the face and breathing muscles. It occurs when the immune system attacks the peripheral nerves' myelin sheath.
5. Central Pontine Myelinolysis (CPM): A rare neurological disorder caused by rapid shifts in sodium levels in the blood, leading to damage to the myelin sheath in a specific area of the brainstem called the pons.

These diseases can result in various symptoms, such as muscle weakness, numbness, vision loss, difficulty with balance and coordination, and cognitive impairment, depending on the location and extent of the demyelination. Treatment typically focuses on managing symptoms, modifying the immune system's response, and promoting nerve regeneration and remyelination when possible.

An axon is a long, slender extension of a neuron (a type of nerve cell) that conducts electrical impulses (nerve impulses) away from the cell body to target cells, such as other neurons or muscle cells. Axons can vary in length from a few micrometers to over a meter long and are typically surrounded by a myelin sheath, which helps to insulate and protect the axon and allows for faster transmission of nerve impulses.

Axons play a critical role in the functioning of the nervous system, as they provide the means by which neurons communicate with one another and with other cells in the body. Damage to axons can result in serious neurological problems, such as those seen in spinal cord injuries or neurodegenerative diseases like multiple sclerosis.

Peripheral nerves are nerve fibers that transmit signals between the central nervous system (CNS, consisting of the brain and spinal cord) and the rest of the body. These nerves convey motor, sensory, and autonomic information, enabling us to move, feel, and respond to changes in our environment. They form a complex network that extends from the CNS to muscles, glands, skin, and internal organs, allowing for coordinated responses and functions throughout the body. Damage or injury to peripheral nerves can result in various neurological symptoms, such as numbness, weakness, or pain, depending on the type and severity of the damage.

Ranvier's nodes, also known as nodes of Ranvier, are specialized structures in the nervous system. They are gaps in the myelin sheath, a fatty insulating substance that surrounds the axons of many neurons, leaving them exposed. These nodes play a crucial role in the rapid transmission of electrical signals along the neuron. The unmyelinated sections of the axon at the nodes have a higher concentration of voltage-gated sodium channels, which generate the action potential that propagates along the neuron. The myelinated segments between the nodes, called internodes, help to speed up this process by allowing the action potential to "jump" from node to node, a mechanism known as saltatory conduction. This process significantly increases the speed of neural impulse transmission, making it more efficient. Ranvier's nodes are named after Louis-Antoine Ranvier, a French histologist and physiologist who first described them in the late 19th century.

The Central Nervous System (CNS) is the part of the nervous system that consists of the brain and spinal cord. It is called the "central" system because it receives information from, and sends information to, the rest of the body through peripheral nerves, which make up the Peripheral Nervous System (PNS).

The CNS is responsible for processing sensory information, controlling motor functions, and regulating various autonomic processes like heart rate, respiration, and digestion. The brain, as the command center of the CNS, interprets sensory stimuli, formulates thoughts, and initiates actions. The spinal cord serves as a conduit for nerve impulses traveling to and from the brain and the rest of the body.

The CNS is protected by several structures, including the skull (which houses the brain) and the vertebral column (which surrounds and protects the spinal cord). Despite these protective measures, the CNS remains vulnerable to injury and disease, which can have severe consequences due to its crucial role in controlling essential bodily functions.

Nerve sheath neoplasms are a group of tumors that arise from the cells surrounding and supporting the nerves. These tumors can be benign or malignant and include schwannomas, neurofibromas, and malignant peripheral nerve sheath tumors (MPNSTs). Schwannomas develop from the Schwann cells that produce the myelin sheath of the nerve, while neurofibromas arise from the nerve's supporting cells called fibroblasts. MPNSTs are cancerous tumors that can grow rapidly and invade surrounding tissues. Nerve sheath neoplasms can cause various symptoms depending on their location and size, including pain, numbness, weakness, or paralysis in the affected area.

2,3'-Cyclic Nucleotide 3'-Phosphodiesterase (CNP) is an enzyme that specifically hydrolyzes 2',3'-cyclic nucleotides to 2'-nucleotide monophosphates. It plays a crucial role in regulating the levels of intracellular second messengers, such as cyclic guanosine monophosphate (cGMP) and cyclic adenosine monophosphate (cAMP), which are involved in various cellular processes including signal transduction, gene expression, and metabolism.

CNP has two isoforms, CNP1 and CNP2, which differ in their tissue distribution and substrate specificity. CNP1 is predominantly expressed in the central nervous system (CNS) and preferentially hydrolyzes cGMP, while CNP2 is widely distributed and hydrolyzes both cGMP and cAMP with similar efficiency.

Mutations in the gene encoding CNP1 have been associated with certain neurological disorders, such as spastic paraplegia type 5 (SPG5), a hereditary condition characterized by progressive muscle weakness and stiffness in the lower limbs.

Myelin-Associated Glycoprotein (MAG) is a glycoprotein found on the surface of myelin sheaths, which are the protective insulating layers around nerve fibers in the nervous system. MAG plays a role in the adhesion and interaction between the myelin sheath and the axon it surrounds. It's particularly important during the development and maintenance of the nervous system. Additionally, MAG has been implicated in the regulation of neuronal growth and signal transmission. In certain autoimmune diseases like Guillain-Barré syndrome, the immune system may mistakenly attack MAG, leading to damage of the myelin sheath and associated neurological symptoms.

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

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

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

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

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

The optic nerve, also known as the second cranial nerve, is the nerve that transmits visual information from the retina to the brain. It is composed of approximately one million nerve fibers that carry signals related to vision, such as light intensity and color, from the eye's photoreceptor cells (rods and cones) to the visual cortex in the brain. The optic nerve is responsible for carrying this visual information so that it can be processed and interpreted by the brain, allowing us to see and perceive our surroundings. Damage to the optic nerve can result in vision loss or impairment.

Wallerian degeneration is a process that occurs following damage to the axons of neurons (nerve cells). After an axon is severed or traumatically injured, it undergoes a series of changes including fragmentation and removal of the distal segment of the axon, which is the part that is separated from the cell body. This process is named after Augustus Waller, who first described it in 1850.

The degenerative changes in the distal axon are characterized by the breakdown of the axonal cytoskeleton, the loss of myelin sheath (the fatty insulating material that surrounds and protects the axon), and the infiltration of macrophages to clear away the debris. These events lead to the degeneration of the distal axon segment, which is necessary for successful regeneration of the injured nerve.

Wallerian degeneration is a crucial process in the nervous system's response to injury, as it enables the regrowth of axons and the reestablishment of connections between neurons. However, if the regenerative capacity of the neuron is insufficient or the environment is not conducive to growth, functional recovery may be impaired, leading to long-term neurological deficits.

The spinal cord is a major part of the nervous system, extending from the brainstem and continuing down to the lower back. It is a slender, tubular bundle of nerve fibers (axons) and support cells (glial cells) that carries signals between the brain and the rest of the body. The spinal cord primarily serves as a conduit for motor information, which travels from the brain to the muscles, and sensory information, which travels from the body to the brain. It also contains neurons that can independently process and respond to information within the spinal cord without direct input from the brain.

The spinal cord is protected by the bony vertebral column (spine) and is divided into 31 segments: 8 cervical, 12 thoracic, 5 lumbar, 5 sacral, and 1 coccygeal. Each segment corresponds to a specific region of the body and gives rise to pairs of spinal nerves that exit through the intervertebral foramina at each level.

The spinal cord is responsible for several vital functions, including:

1. Reflexes: Simple reflex actions, such as the withdrawal reflex when touching a hot surface, are mediated by the spinal cord without involving the brain.
2. Muscle control: The spinal cord carries motor signals from the brain to the muscles, enabling voluntary movement and muscle tone regulation.
3. Sensory perception: The spinal cord transmits sensory information, such as touch, temperature, pain, and vibration, from the body to the brain for processing and awareness.
4. Autonomic functions: The sympathetic and parasympathetic divisions of the autonomic nervous system originate in the thoracolumbar and sacral regions of the spinal cord, respectively, controlling involuntary physiological responses like heart rate, blood pressure, digestion, and respiration.

Damage to the spinal cord can result in various degrees of paralysis or loss of sensation below the level of injury, depending on the severity and location of the damage.

A neurilemma, also known as a schwannoma or neurolemmoma, is a type of benign tumor that arises from the nerve sheath. Specifically, it develops from the Schwann cells, which produce the myelin sheath that insulates and protects the nerves. Neurilemmomas can occur anywhere in the body where there are nerves, but they most commonly affect the cranial nerves, particularly the eighth cranial nerve (the vestibulocochlear nerve). They can also be found along the spine and in the extremities.

Neurilemmomas typically appear as solitary, slow-growing, and well-circumscribed masses that do not usually cause pain or other symptoms unless they compress nearby structures. In some cases, however, they may cause hearing loss, tinnitus, balance problems, or facial nerve paralysis when they affect the cranial nerves. Treatment typically involves surgical removal of the tumor, and the prognosis is generally good, with a low risk of recurrence.

Nerve regeneration is the process of regrowth and restoration of functional nerve connections following damage or injury to the nervous system. This complex process involves various cellular and molecular events, such as the activation of support cells called glia, the sprouting of surviving nerve fibers (axons), and the reformation of neural circuits. The goal of nerve regeneration is to enable the restoration of normal sensory, motor, and autonomic functions impaired due to nerve damage or injury.

I'm sorry for any confusion, but "Jimpy" is not a recognized medical term or condition associated with mice in the field of veterinary medicine. It may be a colloquial or informal term used to describe a particular characteristic or behavior in mice, but without further context, it's challenging to provide an accurate definition. If you could provide more information about where you encountered this term or its intended meaning, I would be happy to help you further.

Neural conduction is the process by which electrical signals, known as action potentials, are transmitted along the axon of a neuron (nerve cell) to transmit information between different parts of the nervous system. This electrical impulse is generated by the movement of ions across the neuronal membrane, and it propagates down the length of the axon until it reaches the synapse, where it can then stimulate the release of neurotransmitters to communicate with other neurons or target cells. The speed of neural conduction can vary depending on factors such as the diameter of the axon, the presence of myelin sheaths (which act as insulation and allow for faster conduction), and the temperature of the environment.

The Peripheral Nervous System (PNS) is that part of the nervous system which lies outside of the brain and spinal cord. It includes all the nerves and ganglia ( clusters of neurons) outside of the central nervous system (CNS). The PNS is divided into two components: the somatic nervous system and the autonomic nervous system.

The somatic nervous system is responsible for transmitting sensory information from the skin, muscles, and joints to the CNS, and for controlling voluntary movements of the skeletal muscles.

The autonomic nervous system, on the other hand, controls involuntary actions, such as heart rate, digestion, respiratory rate, salivation, perspiration, pupillary dilation, and sexual arousal. It is further divided into the sympathetic and parasympathetic systems, which generally have opposing effects and maintain homeostasis in the body.

Damage to the peripheral nervous system can result in various medical conditions such as neuropathies, neuritis, plexopathies, and radiculopathies, leading to symptoms like numbness, tingling, pain, weakness, or loss of reflexes in the affected area.

Sulfoglycosphingolipids are a type of glycosphingolipid that contain a sulfate ester group in their carbohydrate moiety. They are important components of animal cell membranes and play a role in various biological processes, including cell recognition, signal transduction, and cell adhesion.

The most well-known sulfoglycosphingolipids are the sulfatides, which contain a 3'-sulfate ester on the galactose residue of the glycosphingolipid GalCer (galactosylceramide). Sulfatides are abundant in the nervous system and have been implicated in various neurological disorders.

Other sulfoglycosphingolipids include the seminolipids, which contain a 3'-sulfate ester on the galactose residue of lactosylceramide (Galβ1-4Glcβ1-Cer), and are found in high concentrations in the testis.

Abnormalities in sulfoglycosphingolipid metabolism have been associated with several genetic disorders, such as metachromatic leukodystrophy (MLD) and globoid cell leukodystrophy (GLD), which are characterized by progressive neurological deterioration.

Ganglioside Galactosyltransferase is a type of enzyme that plays a role in the biosynthesis of gangliosides, which are complex glycosphingolipids found in high concentrations in the outer leaflet of the plasma membrane of cells, particularly in the nervous system.

Gangliosides contain one or more sialic acid residues and are involved in various cellular processes such as cell recognition, signal transduction, and cell adhesion. The enzyme Ganglioside Galactosyltransferase catalyzes the transfer of a galactose molecule from a donor (usually UDP-galactose) to an acceptor molecule, which is a specific ganglioside substrate.

The reaction facilitated by Ganglioside Galactosyltransferase results in the formation of a new glycosidic bond and the production of more complex gangliosides. Defects in this enzyme have been associated with certain neurological disorders, highlighting its importance in maintaining normal brain function.

Charcot-Marie-Tooth disease (CMT) is a group of inherited disorders that cause nerve damage, primarily affecting the peripheral nerves. These are the nerves that transmit signals between the brain and spinal cord to the rest of the body. CMT affects both motor and sensory nerves, leading to muscle weakness and atrophy, as well as numbness or tingling in the hands and feet.

The disease is named after the three physicians who first described it: Jean-Martin Charcot, Pierre Marie, and Howard Henry Tooth. CMT is characterized by its progressive nature, meaning symptoms typically worsen over time, although the rate of progression can vary significantly among individuals.

There are several types of CMT, classified based on their genetic causes and patterns of inheritance. The two most common forms are CMT1 and CMT2:

1. CMT1: This form is caused by mutations in the genes responsible for the myelin sheath, which insulates peripheral nerves and allows for efficient signal transmission. As a result, demyelination occurs, slowing down nerve impulses and causing muscle weakness, particularly in the lower limbs. Symptoms usually begin in childhood or adolescence and include foot drop, high arches, and hammertoes.
2. CMT2: This form is caused by mutations in the genes responsible for the axons, the nerve fibers that transmit signals within peripheral nerves. As a result, axonal degeneration occurs, leading to muscle weakness and atrophy. Symptoms usually begin in early adulthood and progress more slowly than CMT1. They primarily affect the lower limbs but can also involve the hands and arms.

Diagnosis of CMT typically involves a combination of clinical evaluation, family history, nerve conduction studies, and genetic testing. While there is no cure for CMT, treatment focuses on managing symptoms and maintaining mobility and function through physical therapy, bracing, orthopedic surgery, and pain management.

2,3'-Cyclic-nucleotide phosphodiesterases (PDEs) are a subclass of enzymes that belong to the family of phosphodiesterases. These enzymes are responsible for the hydrolysis of 2,3'-cyclic nucleotides, which are cyclic forms of nucleotides that act as second messengers in various cellular signaling pathways.

The two primary types of 2,3'-cyclic nucleotides are 2',3'-cGMP and 2',3'-cAMP, which are produced by the action of certain enzymes on their respective precursors, guanosine triphosphate (GTP) and adenosine triphosphate (ATP). These cyclic nucleotides play important roles in regulating various cellular processes, including metabolism, gene expression, and ion channel activity.

2,3'-Cyclic-nucleotide phosphodiesterases catalyze the hydrolysis of these cyclic nucleotides to their corresponding 5'-monophosphates, thereby terminating their signaling activity. There are several isoforms of 2,3'-cyclic-nucleotide PDEs that have been identified, each with distinct substrate specificities and regulatory properties.

Dysregulation of 2,3'-cyclic-nucleotide PDE activity has been implicated in various diseases, including cancer, cardiovascular disease, and neurological disorders. Therefore, these enzymes have emerged as important targets for the development of therapeutic agents that can modulate their activity and restore normal cellular function.

The sural nerve is a purely sensory peripheral nerve in the lower leg and foot. It provides sensation to the outer ( lateral) aspect of the little toe and the adjacent side of the fourth toe, as well as a small portion of the skin on the back of the leg between the ankle and knee joints.

The sural nerve is formed by the union of branches from the tibial and common fibular nerves (branches of the sciatic nerve) in the lower leg. It runs down the calf, behind the lateral malleolus (the bony prominence on the outside of the ankle), and into the foot.

The sural nerve is often used as a donor nerve during nerve grafting procedures due to its consistent anatomy and relatively low risk for morbidity at the donor site.

Neurologic mutant mice are genetically engineered or spontaneously mutated rodents that are used as models to study various neurological disorders and conditions. These mice have specific genetic modifications or mutations that affect their nervous system, leading to phenotypes that resemble human neurological diseases.

Some examples of neurologic mutant mice include:

1. Alzheimer's disease models: Mice that overexpress genes associated with Alzheimer's disease, such as the amyloid precursor protein (APP) or presenilin 1 (PS1), to study the pathogenesis and potential treatments of this disorder.
2. Parkinson's disease models: Mice that have genetic mutations in genes associated with Parkinson's disease, such as alpha-synuclein or parkin, to investigate the mechanisms underlying this condition and develop new therapies.
3. Huntington's disease models: Mice that carry an expanded CAG repeat in the huntingtin gene to replicate the genetic defect seen in humans with Huntington's disease and study disease progression and treatment strategies.
4. Epilepsy models: Mice with genetic mutations that cause spontaneous seizures or increased susceptibility to seizures, used to investigate the underlying mechanisms of epilepsy and develop new treatments.
5. Stroke models: Mice that have surgical induction of stroke or genetic modifications that increase the risk of stroke, used to study the pathophysiology of stroke and identify potential therapeutic targets.

Neurologic mutant mice are essential tools in biomedical research, allowing scientists to investigate the complex interactions between genes and the environment that contribute to neurological disorders. These models help researchers better understand disease mechanisms, develop new therapies, and test their safety and efficacy before moving on to clinical trials in humans.

Multiple Sclerosis (MS) is a chronic autoimmune disease that affects the central nervous system (CNS), which includes the brain, spinal cord, and optic nerves. In MS, the immune system mistakenly attacks the protective covering of nerve fibers, called myelin, leading to damage and scarring (sclerosis). This results in disrupted communication between the brain and the rest of the body, causing a variety of neurological symptoms that can vary widely from person to person.

The term "multiple" refers to the numerous areas of scarring that occur throughout the CNS in this condition. The progression, severity, and specific symptoms of MS are unpredictable and may include vision problems, muscle weakness, numbness or tingling, difficulty with balance and coordination, cognitive impairment, and mood changes. There is currently no cure for MS, but various treatments can help manage symptoms, modify the course of the disease, and improve quality of life for those affected.

Transmission electron microscopy (TEM) is a type of microscopy in which an electron beam is transmitted through a ultra-thin specimen, interacting with it as it passes through. An image is formed from the interaction of the electrons with the specimen; the image is then magnified and visualized on a fluorescent screen or recorded on an electronic detector (or photographic film in older models).

TEM can provide high-resolution, high-magnification images that can reveal the internal structure of specimens including cells, viruses, and even molecules. It is widely used in biological and materials science research to investigate the ultrastructure of cells, tissues and materials. In medicine, TEM is used for diagnostic purposes in fields such as virology and bacteriology.

It's important to note that preparing a sample for TEM is a complex process, requiring specialized techniques to create thin (50-100 nm) specimens. These include cutting ultrathin sections of embedded samples using an ultramicrotome, staining with heavy metal salts, and positive staining or negative staining methods.

Early Growth Response Protein 2 (EGR2) is a transcription factor that belongs to the EGR family of proteins, which are involved in various biological processes such as cell proliferation, differentiation, and apoptosis. EGR2 is specifically known to play crucial roles in the development and function of the nervous system, including the regulation of neuronal survival, axon guidance, and myelination. It is also expressed in immune cells and has been implicated in the regulation of immune responses. Mutations in the EGR2 gene have been associated with certain neurological disorders and diseases, such as Charcot-Marie-Tooth disease type 1B and congenital hypomyelinating neuropathy.

Nerve degeneration, also known as neurodegeneration, is the progressive loss of structure and function of neurons, which can lead to cognitive decline, motor impairment, and various other symptoms. This process occurs due to a variety of factors, including genetics, environmental influences, and aging. It is a key feature in several neurological disorders such as Alzheimer's disease, Parkinson's disease, Huntington's disease, and multiple sclerosis. The degeneration can affect any part of the nervous system, leading to different symptoms depending on the location and extent of the damage.

Neuroglia, also known as glial cells or simply glia, are non-neuronal cells that provide support and protection for neurons in the nervous system. They maintain homeostasis, form myelin sheaths around nerve fibers, and provide structural support. They also play a role in the immune response of the central nervous system. Some types of neuroglia include astrocytes, oligodendrocytes, microglia, and ependymal cells.

The brain is the central organ of the nervous system, responsible for receiving and processing sensory information, regulating vital functions, and controlling behavior, movement, and cognition. It is divided into several distinct regions, each with specific functions:

1. Cerebrum: The largest part of the brain, responsible for higher cognitive functions such as thinking, learning, memory, language, and perception. It is divided into two hemispheres, each controlling the opposite side of the body.
2. Cerebellum: Located at the back of the brain, it is responsible for coordinating muscle movements, maintaining balance, and fine-tuning motor skills.
3. Brainstem: Connects the cerebrum and cerebellum to the spinal cord, controlling vital functions such as breathing, heart rate, and blood pressure. It also serves as a relay center for sensory information and motor commands between the brain and the rest of the body.
4. Diencephalon: A region that includes the thalamus (a major sensory relay station) and hypothalamus (regulates hormones, temperature, hunger, thirst, and sleep).
5. Limbic system: A group of structures involved in emotional processing, memory formation, and motivation, including the hippocampus, amygdala, and cingulate gyrus.

The brain is composed of billions of interconnected neurons that communicate through electrical and chemical signals. It is protected by the skull and surrounded by three layers of membranes called meninges, as well as cerebrospinal fluid that provides cushioning and nutrients.

Myelin-Oligodendrocyte Glycoprotein (MOG) is a protein found exclusively on the outermost layer of myelin sheath in the central nervous system (CNS). The myelin sheath is a fatty substance that surrounds and insulates nerve fibers, allowing for efficient and rapid transmission of electrical signals. MOG plays a crucial role in maintaining the integrity and structure of the myelin sheath. It is involved in the adhesion of oligodendrocytes to the surface of neuronal axons and contributes to the stability of the compact myelin structure. Autoimmune reactions against MOG have been implicated in certain inflammatory demyelinating diseases, such as optic neuritis, transverse myelitis, and acute disseminated encephalomyelitis (ADEM).

Cerebrosides are a type of sphingolipid, which are lipids that contain sphingosine. They are major components of the outer layer of cell membranes and are particularly abundant in the nervous system. Cerebrosides are composed of a ceramide molecule (a fatty acid attached to sphingosine) and a sugar molecule, usually either glucose or galactose.

Glycosphingolipids that contain a ceramide with a single sugar residue are called cerebrosides. Those that contain more complex oligosaccharide chains are called gangliosides. Cerebrosides play important roles in cell recognition, signal transduction, and cell adhesion.

Abnormalities in the metabolism of cerebrosides can lead to various genetic disorders, such as Gaucher's disease, Krabbe disease, and Fabry disease. These conditions are characterized by the accumulation of cerebrosides or their breakdown products in various tissues, leading to progressive damage and dysfunction.

Autoimmune encephalomyelitis (EAE) is a model of inflammatory demyelinating disease used in medical research to study the mechanisms of multiple sclerosis (MS) and develop new therapies. It is experimentally induced in laboratory animals, typically mice or rats, through immunization with myelin antigens or T-cell transfer. The resulting immune response leads to inflammation, demyelination, and neurological dysfunction in the central nervous system (CNS), mimicking certain aspects of MS.

EAE is a valuable tool for understanding the pathogenesis of MS and testing potential treatments. However, it is essential to recognize that EAE is an experimental model and may not fully recapitulate all features of human autoimmune encephalomyelitis.

Histological techniques are a set of laboratory methods and procedures used to study the microscopic structure of tissues, also known as histology. These techniques include:

1. Tissue fixation: The process of preserving tissue specimens to maintain their structural integrity and prevent decomposition. This is typically done using formaldehyde or other chemical fixatives.
2. Tissue processing: The preparation of fixed tissues for embedding by removing water, fat, and other substances that can interfere with sectioning and staining. This is usually accomplished through a series of dehydration, clearing, and infiltration steps.
3. Embedding: The placement of processed tissue specimens into a solid support medium, such as paraffin or plastic, to facilitate sectioning.
4. Sectioning: The cutting of thin slices (usually 4-6 microns thick) from embedded tissue blocks using a microtome.
5. Staining: The application of dyes or stains to tissue sections to highlight specific structures or components. This can be done through a variety of methods, including hematoxylin and eosin (H&E) staining, immunohistochemistry, and special stains for specific cell types or molecules.
6. Mounting: The placement of stained tissue sections onto glass slides and covering them with a mounting medium to protect the tissue from damage and improve microscopic visualization.
7. Microscopy: The examination of stained tissue sections using a light or electron microscope to observe and analyze their structure and composition.

These techniques are essential for the diagnosis and study of various diseases, including cancer, neurological disorders, and infections. They allow pathologists and researchers to visualize and understand the cellular and molecular changes that occur in tissues during disease processes.

Hereditary Sensory and Motor Neuropathy (HSMN) is a group of inherited disorders that affect the peripheral nerves, which are the nerves outside the brain and spinal cord. These nerves transmit information between the brain and muscles, as well as sensations such as touch, pain, heat, and cold.

HSMN is characterized by progressive degeneration of these peripheral nerves, leading to muscle weakness, numbness, and tingling sensations, particularly in the hands and feet. The condition can also affect the autonomic nervous system, which controls involuntary functions such as heart rate, blood pressure, and digestion.

HSMN is caused by genetic mutations that are inherited from one or both parents. There are several types of HSMN, each with its own specific symptoms, severity, and pattern of inheritance. The most common form is Charcot-Marie-Tooth disease (CMT), which affects both motor and sensory nerves.

Treatment for HSMN typically focuses on managing the symptoms and preventing complications. This may include physical therapy, bracing or orthopedic surgery to support weakened muscles, pain management, and lifestyle modifications such as avoiding activities that aggravate symptoms. There is currently no cure for HSMN, but ongoing research is aimed at developing new treatments and therapies to slow or halt the progression of the disease.

Spinal nerve roots are the initial parts of spinal nerves that emerge from the spinal cord through the intervertebral foramen, which are small openings between each vertebra in the spine. These nerve roots carry motor, sensory, and autonomic fibers to and from specific regions of the body. There are 31 pairs of spinal nerve roots in total, with 8 cervical, 12 thoracic, 5 lumbar, 5 sacral, and 1 coccygeal pair. Each root has a dorsal (posterior) and ventral (anterior) ramus that branch off to form the peripheral nervous system. Irritation or compression of these nerve roots can result in pain, numbness, weakness, or loss of reflexes in the affected area.

Neuregulin-1 (NRG-1) is a growth factor that belongs to the neuregulin family and is involved in the development and function of the nervous system. It is a protein that is encoded by the NRG1 gene and is expressed in various tissues, including the brain. NRG-1 plays important roles in the regulation of neuronal survival, migration, differentiation, and synaptic plasticity. It acts as a ligand for the ErbB family of receptor tyrosine kinases, which are involved in intracellular signaling pathways that control various cellular processes. Abnormalities in NRG-1 signaling have been implicated in several neurological and psychiatric disorders, including schizophrenia, bipolar disorder, and Alzheimer's disease.

Peripheral Nervous System (PNS) diseases, also known as Peripheral Neuropathies, refer to conditions that affect the functioning of the peripheral nervous system, which includes all the nerves outside the brain and spinal cord. These nerves transmit signals between the central nervous system (CNS) and the rest of the body, controlling sensations, movements, and automatic functions such as heart rate and digestion.

PNS diseases can be caused by various factors, including genetics, infections, toxins, metabolic disorders, trauma, or autoimmune conditions. The symptoms of PNS diseases depend on the type and extent of nerve damage but often include:

1. Numbness, tingling, or pain in the hands and feet
2. Muscle weakness or cramps
3. Loss of reflexes
4. Decreased sensation to touch, temperature, or vibration
5. Coordination problems and difficulty with balance
6. Sexual dysfunction
7. Digestive issues, such as constipation or diarrhea
8. Dizziness or fainting due to changes in blood pressure

Examples of PNS diseases include Guillain-Barre syndrome, Charcot-Marie-Tooth disease, diabetic neuropathy, and peripheral nerve injuries. Treatment for these conditions varies depending on the underlying cause but may involve medications, physical therapy, lifestyle changes, or surgery.

Nerve tissue proteins are specialized proteins found in the nervous system that provide structural and functional support to nerve cells, also known as neurons. These proteins include:

1. Neurofilaments: These are type IV intermediate filaments that provide structural support to neurons and help maintain their shape and size. They are composed of three subunits - NFL (light), NFM (medium), and NFH (heavy).

2. Neuronal Cytoskeletal Proteins: These include tubulins, actins, and spectrins that provide structural support to the neuronal cytoskeleton and help maintain its integrity.

3. Neurotransmitter Receptors: These are specialized proteins located on the postsynaptic membrane of neurons that bind neurotransmitters released by presynaptic neurons, triggering a response in the target cell.

4. Ion Channels: These are transmembrane proteins that regulate the flow of ions across the neuronal membrane and play a crucial role in generating and transmitting electrical signals in neurons.

5. Signaling Proteins: These include enzymes, receptors, and adaptor proteins that mediate intracellular signaling pathways involved in neuronal development, differentiation, survival, and death.

6. Adhesion Proteins: These are cell surface proteins that mediate cell-cell and cell-matrix interactions, playing a crucial role in the formation and maintenance of neural circuits.

7. Extracellular Matrix Proteins: These include proteoglycans, laminins, and collagens that provide structural support to nerve tissue and regulate neuronal migration, differentiation, and survival.

"Newborn animals" refers to the very young offspring of animals that have recently been born. In medical terminology, newborns are often referred to as "neonates," and they are classified as such from birth until about 28 days of age. During this time period, newborn animals are particularly vulnerable and require close monitoring and care to ensure their survival and healthy development.

The specific needs of newborn animals can vary widely depending on the species, but generally, they require warmth, nutrition, hydration, and protection from harm. In many cases, newborns are unable to regulate their own body temperature or feed themselves, so they rely heavily on their mothers for care and support.

In medical settings, newborn animals may be examined and treated by veterinarians to ensure that they are healthy and receiving the care they need. This can include providing medical interventions such as feeding tubes, antibiotics, or other treatments as needed to address any health issues that arise. Overall, the care and support of newborn animals is an important aspect of animal medicine and conservation efforts.

Spinal ganglia, also known as dorsal root ganglia, are clusters of nerve cell bodies located in the peripheral nervous system. They are situated along the length of the spinal cord and are responsible for transmitting sensory information from the body to the brain. Each spinal ganglion contains numerous neurons, or nerve cells, with long processes called axons that extend into the periphery and innervate various tissues and organs. The cell bodies within the spinal ganglia receive sensory input from these axons and transmit this information to the central nervous system via the dorsal roots of the spinal nerves. This allows the brain to interpret and respond to a wide range of sensory stimuli, including touch, temperature, pain, and proprioception (the sense of the position and movement of one's body).

Biometry, also known as biometrics, is the scientific study of measurements and statistical analysis of living organisms. In a medical context, biometry is often used to refer to the measurement and analysis of physical characteristics or features of the human body, such as height, weight, blood pressure, heart rate, and other physiological variables. These measurements can be used for a variety of purposes, including diagnosis, treatment planning, monitoring disease progression, and research.

In addition to physical measurements, biometry may also refer to the use of statistical methods to analyze biological data, such as genetic information or medical images. This type of analysis can help researchers and clinicians identify patterns and trends in large datasets, and make predictions about health outcomes or treatment responses.

Overall, biometry is an important tool in modern medicine, as it allows healthcare professionals to make more informed decisions based on data and evidence.

A "knockout" mouse is a genetically engineered mouse in which one or more genes have been deleted or "knocked out" using molecular biology techniques. This allows researchers to study the function of specific genes and their role in various biological processes, as well as potential associations with human diseases. The mice are generated by introducing targeted DNA modifications into embryonic stem cells, which are then used to create a live animal. Knockout mice have been widely used in biomedical research to investigate gene function, disease mechanisms, and potential therapeutic targets.

Nerve fibers are specialized structures that constitute the long, slender processes (axons) of neurons (nerve cells). They are responsible for conducting electrical impulses, known as action potentials, away from the cell body and transmitting them to other neurons or effector organs such as muscles and glands. Nerve fibers are often surrounded by supportive cells called glial cells and are grouped together to form nerve bundles or nerves. These fibers can be myelinated (covered with a fatty insulating sheath called myelin) or unmyelinated, which influences the speed of impulse transmission.

The corpus callosum is the largest collection of white matter in the brain, consisting of approximately 200 million nerve fibers. It is a broad, flat band of tissue that connects the two hemispheres of the brain, allowing them to communicate and coordinate information processing. The corpus callosum plays a crucial role in integrating sensory, motor, and cognitive functions between the two sides of the brain. Damage to the corpus callosum can result in various neurological symptoms, including difficulties with movement, speech, memory, and social behavior.

Immunohistochemistry (IHC) is a technique used in pathology and laboratory medicine to identify specific proteins or antigens in tissue sections. It combines the principles of immunology and histology to detect the presence and location of these target molecules within cells and tissues. This technique utilizes antibodies that are specific to the protein or antigen of interest, which are then tagged with a detection system such as a chromogen or fluorophore. The stained tissue sections can be examined under a microscope, allowing for the visualization and analysis of the distribution and expression patterns of the target molecule in the context of the tissue architecture. Immunohistochemistry is widely used in diagnostic pathology to help identify various diseases, including cancer, infectious diseases, and immune-mediated disorders.

Brain chemistry refers to the chemical processes that occur within the brain, particularly those involving neurotransmitters, neuromodulators, and neuropeptides. These chemicals are responsible for transmitting signals between neurons (nerve cells) in the brain, allowing for various cognitive, emotional, and physical functions.

Neurotransmitters are chemical messengers that transmit signals across the synapse (the tiny gap between two neurons). Examples of neurotransmitters include dopamine, serotonin, norepinephrine, GABA (gamma-aminobutyric acid), and glutamate. Each neurotransmitter has a specific role in brain function, such as regulating mood, motivation, attention, memory, and movement.

Neuromodulators are chemicals that modify the effects of neurotransmitters on neurons. They can enhance or inhibit the transmission of signals between neurons, thereby modulating brain activity. Examples of neuromodulators include acetylcholine, histamine, and substance P.

Neuropeptides are small protein-like molecules that act as neurotransmitters or neuromodulators. They play a role in various physiological functions, such as pain perception, stress response, and reward processing. Examples of neuropeptides include endorphins, enkephalins, and oxytocin.

Abnormalities in brain chemistry can lead to various neurological and psychiatric conditions, such as depression, anxiety disorders, schizophrenia, Parkinson's disease, and Alzheimer's disease. Understanding brain chemistry is crucial for developing effective treatments for these conditions.

Neurofilament proteins (NFs) are type IV intermediate filament proteins that are specific to neurons. They are the major structural components of the neuronal cytoskeleton and play crucial roles in maintaining the structural integrity, stability, and diameter of axons. Neurofilaments are composed of three subunits: light (NFL), medium (NFM), and heavy (NFH) neurofilament proteins, which differ in their molecular weights. These subunits assemble into heteropolymers to form the neurofilament core, while the C-terminal tails of NFH and NFM extend outward from the core, interacting with other cellular components and participating in various neuronal functions. Increased levels of neurofilament proteins, particularly NFL, in cerebrospinal fluid (CSF) and blood are considered biomarkers for axonal damage and neurodegeneration in several neurological disorders, such as Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis (ALS), and multiple sclerosis (MS).

Galactosylceramides are a type of glycosphingolipids, which are lipid molecules that contain a sugar (glyco-) attached to a ceramide. Galactosylceramides have a galactose molecule attached to the ceramide. They are important components of cell membranes and play a role in cell recognition and signaling. In particular, they are abundant in the myelin sheath, which is the protective covering around nerve fibers in the brain and spinal cord. Abnormal accumulation of galactosylceramides can lead to certain genetic disorders, such as Krabbe disease and Gaucher disease.

Transgenic mice are genetically modified rodents that have incorporated foreign DNA (exogenous DNA) into their own genome. This is typically done through the use of recombinant DNA technology, where a specific gene or genetic sequence of interest is isolated and then introduced into the mouse embryo. The resulting transgenic mice can then express the protein encoded by the foreign gene, allowing researchers to study its function in a living organism.

The process of creating transgenic mice usually involves microinjecting the exogenous DNA into the pronucleus of a fertilized egg, which is then implanted into a surrogate mother. The offspring that result from this procedure are screened for the presence of the foreign DNA, and those that carry the desired genetic modification are used to establish a transgenic mouse line.

Transgenic mice have been widely used in biomedical research to model human diseases, study gene function, and test new therapies. They provide a valuable tool for understanding complex biological processes and developing new treatments for a variety of medical conditions.

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

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

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

Animal disease models are specialized animals, typically rodents such as mice or rats, that have been genetically engineered or exposed to certain conditions to develop symptoms and physiological changes similar to those seen in human diseases. These models are used in medical research to study the pathophysiology of diseases, identify potential therapeutic targets, test drug efficacy and safety, and understand disease mechanisms.

The genetic modifications can include knockout or knock-in mutations, transgenic expression of specific genes, or RNA interference techniques. The animals may also be exposed to environmental factors such as chemicals, radiation, or infectious agents to induce the disease state.

Examples of animal disease models include:

1. Mouse models of cancer: Genetically engineered mice that develop various types of tumors, allowing researchers to study cancer initiation, progression, and metastasis.
2. Alzheimer's disease models: Transgenic mice expressing mutant human genes associated with Alzheimer's disease, which exhibit amyloid plaque formation and cognitive decline.
3. Diabetes models: Obese and diabetic mouse strains like the NOD (non-obese diabetic) or db/db mice, used to study the development of type 1 and type 2 diabetes, respectively.
4. Cardiovascular disease models: Atherosclerosis-prone mice, such as ApoE-deficient or LDLR-deficient mice, that develop plaque buildup in their arteries when fed a high-fat diet.
5. Inflammatory bowel disease models: Mice with genetic mutations affecting intestinal barrier function and immune response, such as IL-10 knockout or SAMP1/YitFc mice, which develop colitis.

Animal disease models are essential tools in preclinical research, but it is important to recognize their limitations. Differences between species can affect the translatability of results from animal studies to human patients. Therefore, researchers must carefully consider the choice of model and interpret findings cautiously when applying them to human diseases.

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

Immunoelectron microscopy (IEM) is a specialized type of electron microscopy that combines the principles of immunochemistry and electron microscopy to detect and localize specific antigens within cells or tissues at the ultrastructural level. This technique allows for the visualization and identification of specific proteins, viruses, or other antigenic structures with a high degree of resolution and specificity.

In IEM, samples are first fixed, embedded, and sectioned to prepare them for electron microscopy. The sections are then treated with specific antibodies that have been labeled with electron-dense markers, such as gold particles or ferritin. These labeled antibodies bind to the target antigens in the sample, allowing for their visualization under an electron microscope.

There are several different methods of IEM, including pre-embedding and post-embedding techniques. Pre-embedding involves labeling the antigens before embedding the sample in resin, while post-embedding involves labeling the antigens after embedding. Post-embedding techniques are generally more commonly used because they allow for better preservation of ultrastructure and higher resolution.

IEM is a valuable tool in many areas of research, including virology, bacteriology, immunology, and cell biology. It can be used to study the structure and function of viruses, bacteria, and other microorganisms, as well as the distribution and localization of specific proteins and antigens within cells and tissues.

C57BL/6 (C57 Black 6) is an inbred strain of laboratory mouse that is widely used in biomedical research. The term "inbred" refers to a strain of animals where matings have been carried out between siblings or other closely related individuals for many generations, resulting in a population that is highly homozygous at most genetic loci.

The C57BL/6 strain was established in 1920 by crossing a female mouse from the dilute brown (DBA) strain with a male mouse from the black strain. The resulting offspring were then interbred for many generations to create the inbred C57BL/6 strain.

C57BL/6 mice are known for their robust health, longevity, and ease of handling, making them a popular choice for researchers. They have been used in a wide range of biomedical research areas, including studies of cancer, immunology, neuroscience, cardiovascular disease, and metabolism.

One of the most notable features of the C57BL/6 strain is its sensitivity to certain genetic modifications, such as the introduction of mutations that lead to obesity or impaired glucose tolerance. This has made it a valuable tool for studying the genetic basis of complex diseases and traits.

Overall, the C57BL/6 inbred mouse strain is an important model organism in biomedical research, providing a valuable resource for understanding the genetic and molecular mechanisms underlying human health and disease.

Astrocytes are a type of star-shaped glial cell found in the central nervous system (CNS), including the brain and spinal cord. They play crucial roles in supporting and maintaining the health and function of neurons, which are the primary cells responsible for transmitting information in the CNS.

Some of the essential functions of astrocytes include:

1. Supporting neuronal structure and function: Astrocytes provide structural support to neurons by ensheathing them and maintaining the integrity of the blood-brain barrier, which helps regulate the entry and exit of substances into the CNS.
2. Regulating neurotransmitter levels: Astrocytes help control the levels of neurotransmitters in the synaptic cleft (the space between two neurons) by taking up excess neurotransmitters and breaking them down, thus preventing excessive or prolonged activation of neuronal receptors.
3. Providing nutrients to neurons: Astrocytes help supply energy metabolites, such as lactate, to neurons, which are essential for their survival and function.
4. Modulating synaptic activity: Through the release of various signaling molecules, astrocytes can modulate synaptic strength and plasticity, contributing to learning and memory processes.
5. Participating in immune responses: Astrocytes can respond to CNS injuries or infections by releasing pro-inflammatory cytokines and chemokines, which help recruit immune cells to the site of injury or infection.
6. Promoting neuronal survival and repair: In response to injury or disease, astrocytes can become reactive and undergo morphological changes that aid in forming a glial scar, which helps contain damage and promote tissue repair. Additionally, they release growth factors and other molecules that support the survival and regeneration of injured neurons.

Dysfunction or damage to astrocytes has been implicated in several neurological disorders, including Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis (ALS), and multiple sclerosis (MS).

Cell adhesion molecules (CAMs) are a type of protein that mediates the attachment or binding of cells to their surrounding extracellular matrix or to other cells. Neuronal cell adhesion molecules (NCAMs) are a specific subtype of CAMs that are primarily expressed on neurons and play crucial roles in the development, maintenance, and function of the nervous system.

NCAMs are involved in various processes such as cell recognition, migration, differentiation, synaptic plasticity, and neural circuit formation. They can interact with other NCAMs or other types of CAMs to form homophilic or heterophilic bonds, respectively. The binding of NCAMs can activate intracellular signaling pathways that regulate various cellular responses.

NCAMs are classified into three major families based on their molecular structure: the immunoglobulin superfamily (Ig-CAMs), the cadherin family, and the integrin family. The Ig-CAMs include NCAM1 (also known as CD56), which is a glycoprotein with multiple extracellular Ig-like domains and intracellular signaling motifs. The cadherin family includes N-cadherin, which mediates calcium-dependent cell-cell adhesion. The integrin family includes integrins such as α5β1 and αVβ3, which mediate cell-matrix adhesion.

Abnormalities in NCAMs have been implicated in various neurological disorders, including schizophrenia, Alzheimer's disease, and autism spectrum disorder. Therefore, understanding the structure and function of NCAMs is essential for developing therapeutic strategies to treat these conditions.

Cell differentiation is the process by which a less specialized cell, or stem cell, becomes a more specialized cell type with specific functions and structures. This process involves changes in gene expression, which are regulated by various intracellular signaling pathways and transcription factors. Differentiation results in the development of distinct cell types that make up tissues and organs in multicellular organisms. It is a crucial aspect of embryonic development, tissue repair, and maintenance of homeostasis in the body.

Peripheral nervous system (PNS) neoplasms refer to tumors that originate in the peripheral nerves, which are the nerves outside the brain and spinal cord. These tumors can be benign or malignant (cancerous). Benign tumors, such as schwannomas and neurofibromas, grow slowly and do not spread to other parts of the body. Malignant tumors, such as malignant peripheral nerve sheath tumors (MPNSTs), can invade nearby tissues and may metastasize (spread) to other organs.

PNS neoplasms can cause various symptoms depending on their location and size. Common symptoms include pain, weakness, numbness, or tingling in the affected area. In some cases, PNS neoplasms may not cause any symptoms until they become quite large. Treatment options for PNS neoplasms depend on several factors, including the type, size, and location of the tumor, as well as the patient's overall health. Treatment options may include surgery, radiation therapy, chemotherapy, or a combination of these approaches.

The rectus abdominis is a paired, flat, and long muscle in the anterior (front) wall of the abdomen. It runs from the pubic symphysis (the joint where the two pubic bones meet in the front of the pelvis) to the xiphoid process (the lower end of the sternum or breastbone) and costal cartilages of the fifth, sixth, and seventh ribs.

The rectus abdominis is responsible for flexing the lumbar spine (lower back), which helps in bending forward or sitting up from a lying down position. It also contributes to maintaining proper posture and stabilizing the pelvis and spine. The muscle's visibility, especially in its lower portion, is often associated with a "six-pack" appearance in well-trained individuals.

Neurons, also known as nerve cells or neurocytes, are specialized cells that constitute the basic unit of the nervous system. They are responsible for receiving, processing, and transmitting information and signals within the body. Neurons have three main parts: the dendrites, the cell body (soma), and the axon. The dendrites receive signals from other neurons or sensory receptors, while the axon transmits these signals to other neurons, muscles, or glands. The junction between two neurons is called a synapse, where neurotransmitters are released to transmit the signal across the gap (synaptic cleft) to the next neuron. Neurons vary in size, shape, and structure depending on their function and location within the nervous system.

The cerebellum is a part of the brain that lies behind the brainstem and is involved in the regulation of motor movements, balance, and coordination. It contains two hemispheres and a central portion called the vermis. The cerebellum receives input from sensory systems and other areas of the brain and spinal cord and sends output to motor areas of the brain. Damage to the cerebellum can result in problems with movement, balance, and coordination.

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

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

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

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

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

A neurofibroma is a benign (non-cancerous) tumor that develops from the nerve sheath, which is the protective covering around nerves. These tumors can grow anywhere on the body and can be found under the skin or deep inside the body. Neurofibromas can vary in size, and they may cause symptoms such as pain, numbness, or tingling if they press on nearby nerves.

Neurofibromas are a common feature of neurofibromatosis type 1 (NF1), a genetic disorder that affects approximately 1 in every 3,000 people worldwide. NF1 is characterized by the development of multiple neurofibromas and other tumors, as well as skin changes such as café-au-lait spots and freckling.

It's important to note that while most neurofibromas are benign, they can rarely undergo malignant transformation and become cancerous. If you have a neurofibroma or are concerned about your risk of developing one, it's important to seek medical advice from a healthcare professional who is familiar with this condition.

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

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

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

The Fluorescent Antibody Technique (FAT) is a type of immunofluorescence assay used in laboratory medicine and pathology for the detection and localization of specific antigens or antibodies in tissues, cells, or microorganisms. In this technique, a fluorescein-labeled antibody is used to selectively bind to the target antigen or antibody, forming an immune complex. When excited by light of a specific wavelength, the fluorescein label emits light at a longer wavelength, typically visualized as green fluorescence under a fluorescence microscope.

The FAT is widely used in diagnostic microbiology for the identification and characterization of various bacteria, viruses, fungi, and parasites. It has also been applied in the diagnosis of autoimmune diseases and certain cancers by detecting specific antibodies or antigens in patient samples. The main advantage of FAT is its high sensitivity and specificity, allowing for accurate detection and differentiation of various pathogens and disease markers. However, it requires specialized equipment and trained personnel to perform and interpret the results.

The "sperm tail" is also known as the flagellum, which is a whip-like structure that enables the sperm to move or swim through fluid. The human sperm tail is made up of nine microtubule doublets and a central pair of microtubules, which are surrounded by a mitochondrial sheath that provides energy for its movement. This complex structure allows the sperm to navigate through the female reproductive tract in order to reach and fertilize an egg.

Coculture techniques refer to a type of experimental setup in which two or more different types of cells or organisms are grown and studied together in a shared culture medium. This method allows researchers to examine the interactions between different cell types or species under controlled conditions, and to study how these interactions may influence various biological processes such as growth, gene expression, metabolism, and signal transduction.

Coculture techniques can be used to investigate a wide range of biological phenomena, including the effects of host-microbe interactions on human health and disease, the impact of different cell types on tissue development and homeostasis, and the role of microbial communities in shaping ecosystems. These techniques can also be used to test the efficacy and safety of new drugs or therapies by examining their effects on cells grown in coculture with other relevant cell types.

There are several different ways to establish cocultures, depending on the specific research question and experimental goals. Some common methods include:

1. Mixed cultures: In this approach, two or more cell types are simply mixed together in a culture dish or flask and allowed to grow and interact freely.
2. Cell-layer cultures: Here, one cell type is grown on a porous membrane or other support structure, while the second cell type is grown on top of it, forming a layered coculture.
3. Conditioned media cultures: In this case, one cell type is grown to confluence and its culture medium is collected and then used to grow a second cell type. This allows the second cell type to be exposed to any factors secreted by the first cell type into the medium.
4. Microfluidic cocultures: These involve growing cells in microfabricated channels or chambers, which allow for precise control over the spatial arrangement and flow of nutrients, waste products, and signaling molecules between different cell types.

Overall, coculture techniques provide a powerful tool for studying complex biological systems and gaining insights into the mechanisms that underlie various physiological and pathological processes.

Aging is a complex, progressive and inevitable process of bodily changes over time, characterized by the accumulation of cellular damage and degenerative changes that eventually lead to increased vulnerability to disease and death. It involves various biological, genetic, environmental, and lifestyle factors that contribute to the decline in physical and mental functions. The medical field studies aging through the discipline of gerontology, which aims to understand the underlying mechanisms of aging and develop interventions to promote healthy aging and extend the human healthspan.

The inner mesaxon (Terminologia histologica: Mesaxon internum) is the connection between the myelin sheath and the inner part ... "The Myelin Sheath". Basic Neurochemistry: Molecular, Cellular and Medical Aspects. 6th edition. v t e (All stub articles, ... is the connection of the outer cell membrane to the compact myelin sheath. ...
Morell, Pierre; Quarles, Richard H. (1999). "The Myelin Sheath". Basic Neurochemistry: Molecular, Cellular and Medical Aspects ... The lysosome breaks down acid ceramidase; the fatty acid component is then used to produce myelin. Myelin is an insulating ... The lack of myelin resulting from the lack of acid ceramidase breakdown leads to nerve cell dysfunction.[citation needed] ...
It occurs when the myelin sheath of the nerve cells becomes damaged. As the myelin sheath is responsible for protecting the ... "Myelin Sheath - Definition and Function , Biology Dictionary". Biology Dictionary. 2017-02-10. Retrieved 2018-10-19. " ...
The axon is insulated by a myelin sheath. Myelin is composed of either Schwann cells (in the peripheral nervous system) or ... certain neuronal axons are covered with myelin sheaths. Myelin is a multilamellar membrane that enwraps the axon in segments ... Myelin sheath reduces membrane capacitance and increases membrane resistance in the inter-node intervals, thus allowing a fast ... Dendrite Soma Axon Nucleus Node of Ranvier Axon terminal Schwann cell Myelin sheath Several types of cells support an action ...
This is the provision of an insulating layer, called a myelin sheath. The myelin membrane is unique in its relatively high ... Oligodendrocytes form the insulating myelin in the CNS. Along myelinated nerve fibers, gaps in the myelin sheath known as nodes ... and in the PNS it is myelin basic protein. Nodes of Ranvier (also known as myelin sheath gaps) are short unmyelinated segments ... Hsu K, Terakawa S (July 1996). "Fenestration in the myelin sheath of nerve fibers of the shrimp: a novel node of excitation for ...
Kursula P (Feb 2008). "Structural properties of proteins specific to the myelin sheath". Amino Acids. 34 (2): 175-85. doi: ... phosphate CNPase is a myelin-associated enzyme that makes up 4% of total CNS myelin protein, and is thought to undergo ... Stricker R, Kalbacher H, Reiser G (Aug 1997). "The epitope recognized by a monoclonal antibody in the myelin-associated protein ... Thompson RJ (Aug 1992). "2',3'-cyclic nucleotide-3'-phosphohydrolase and signal transduction in central nervous system myelin ...
In myelinated axons, Schwann cells form the myelin sheath. The sheath is not continuous. Individual myelinating Schwann cells ... Dendrite Soma Axon Nucleus Node of Ranvier Axon terminal Schwann cell Myelin sheath Schwann cells are a variety of glial cells ... Myelinating Schwann cells wrap around axons of motor and sensory neurons to form the myelin sheath. The Schwann cell promoter ... The vertebrate`s nervous system relies on the myelin sheath for insulation and as a method of decreasing membrane capacitance ...
Peterson, Edith R.; Murray, Margaret R. (1955). "Myelin sheath formation in cultures of avian spinal ganglia". American Journal ... Murray and collaborators reported in1940 that peripheral nerve sheath tumors originate from Schwann cells. In 1947, Drs. Murray ... Bornstein, Murray B.; Murray, Margaret R. (1958). "Serial Observations on Patterns of Growth, Myelin Formation, Maintenance and ... "Schwann cell versus fibroblast as the origin of the specific nerve sheath tumor". American Journal of Pathology. 16: 41-60. ...
The myelin sheath allows nerve cells to conduct signals faster. When the myelin sheath is damaged, nerve signals are slower, ... Nerve signals are conducted by an axon with a myelin sheath wrapped around it. Most mutations in CMT affect the myelin sheath, ... CMT2 types are a result of damage to the nerve axons rather than damage to the myelin sheath (as is the case with CMT1). ... Schwann cells create the myelin sheath, by wrapping its plasma membrane around the axon. Neurons, Schwann cells, and ...
... with each axon being wrapped in approximately 1 μm of myelin sheath. Furthermore, an oligodendrocyte can provide myelin ... They are not attached to neurons via myelin sheaths and, therefore, do not contribute to insulation. They remain opposed to ... Mammalian nervous systems depend crucially on myelin sheaths, which reduce ion leakage and decrease the capacitance of the cell ... Oligodendrocytes accomplish this by forming the myelin sheath around axons. Unlike Schwann cells, a single oligodendrocyte can ...
Rather, myelin ensheaths the axon in segments: in general, each axon is encased in multiple long myelin sheaths separated by ... These myelin-like sheaths share several structural features with the sheaths found in vertebrates including multiplicity of ... When a peripheral fiber is severed, the myelin sheath provides a track along which regrowth can occur. However, the myelin ... The MS Information Sourcebook, Myelin H & E Histology Luxol Fast Blue: Modified Kluver's Method to stain for Myelin Sheath (CS1 ...
"Topographical arrangement of membrane proteins in the intact myelin sheath. Lactoperoxidase incorproation of iodine into myelin ...
The oligodendrocytes that originally formed a myelin sheath cannot completely rebuild a destroyed myelin sheath. However, the ... The newly formed myelin sheaths are thinner and often not as effective as the original ones. Repeated attacks lead to ... Myelin sheaths are still intact but swollen. Small increase in microglia and T cells. Active layer: Phagocytic demyelinating ... MS lesions mainly consist in demyelination and scarring in the fatty myelin sheaths around the axons of the brain and spinal ...
Nerve impulses are transmitted by myelin, a fatty material that grows around a cell. White matter has a myelin sheath (a ... The myelin sheath isn't fully formed until around ages 24-26. This means that adolescents and young adults typically learn ... collection of myelin) while gray matter doesn't, which efficiently allows neural impulses to move swiftly along the fiber. ...
... eventually destroying the myelin sheath of the nervous system. The myelin sheath is a fatty covering that protects nerve fibers ... The Myelin Project Multiple sclerosis "metachromatic leukodystrophy" at Dorland's Medical Dictionary Le, Tao; Bhushan, Vikas; ... Leukodystrophies affect the growth and/or development of myelin, the fatty covering which acts as an insulator around nerve ...
Damage occurs to the myelin sheath in the peripheral nervous system. As doctors at the Mayo Clinic were beginning to note, the ... Physiological testing indicated signature antibodies in the mouse model at 100% in potassium channel antibodies and myelin ...
MS will target the protective sheath (myelin) that covers the nerves. Myelin allows for communication. The destruction of ... myelin would result in poor communication between the brain and the body. Those with MS will experience neurological damage ...
Myelin is an insulating sheath around neurons in the spinal cord. One proposed cause of degenerative myelopathy is that the ... immune system attacks this sheath, breaking it down. This results in a loss of communication between nerves in lower body of ...
Demyelinating plaques attack the myelin sheaths on neurons. This decreases the conduction velocity of the neurons, making the ...
While in Japan, he studied vertebrate nerve fibers and discovered the insulating function of the myelin sheath, a material that ... Tasaki is credited with discovering the insulating function of the myelin sheath. His discoveries provided the foundation for a ... between the breaks in the myelin wrapping, called nodes of Ranvier. This process, termed saltatory conduction, is featured in a ... better understanding of diseases such as multiple sclerosis, in which myelin is lost or damaged. In 1910, Tasaki was born in ...
In this disease, the immune system attacks the myelin sheath surrounding neurons. Deterioration of the myelin sheath ...
... on the myelin sheath of the CNS to provide the structural integrity of the myelin sheath." MOG's cDNA coding region in humans ... While the primary molecular function of MOG is not yet known, its likely role with the myelin sheath is either in sheath " ... It is speculated to serve as a necessary "adhesion molecule" to provide structural integrity to the myelin sheath and is known ... "very late on oligodendrocytes and the myelin sheath". Interest in MOG has centered on its role in demyelinating diseases. Some ...
The spinal cord becomes thinner and nerve cells lose some myelin sheath. The diameter of the spinal cord is smaller than that ... The spinal cord becomes thinner, and nerve cells lose some myelin sheath. In February 2023, the first approval of a treatment ...
Myelin forms a layer, the myelin sheath, around the axons and neurons. When this sheath is damaged the transport of action ...
Axons are wrapped in a sheath of Schwann cells that contain myelin. Between Schwann cells are gaps (nodes of Ranvier) where the ... Dendrite Soma Axon Nucleus Node of Ranvier Axon terminal Schwann cell Myelin sheath The nerve dysfunction in Guillain-Barré ... The demyelinating variant (AIDP, see below) features damage to the myelin sheath by white blood cells (T lymphocytes and ... Myelin disorders, Peripheral nervous system disorders, Syndromes affecting the nervous system, Wikipedia medicine articles ...
... s containing a sulfuric ester (sulfate) group, known as sulfatides, also occur in the myelin sheath of nerves. These ... Monogalactosylceramide is the largest single component of the myelin sheath of nerves. Cerebroside synthesis can therefore give ... a measurement of myelin formation or remyelination. The sugar moiety is linked glycosidically to the C-1 hydroxyl group of ...
For example, sphingomyelin is part of the myelin sheath of nerve fibers. Sphingolipids are formed from ceramides that consist ...
"Frequency moving to test agents with remyelination potential , FREQ-162 among compounds that might restore myelin sheath in MS ... activates oligodendrocyte progenitor cells in the central nervous system to generate new oligodendrocytes and regenerate myelin ...
... but in white matter the principal barrier is the myelin sheath of axons. Bundles of axons provide a barrier to perpendicular ... Conditions where the myelin or the structure of the axon are disrupted, such as trauma, tumors, and inflammation reduce ... Barriers can be many things: cell membranes, axons, myelin, etc.; ...
PMP22/gas-3, called peripheral myelin protein, is located in the myelin sheath. The expression of this protein is associated ... In the central and peripheral nervous system are TJ localized between a glia and an axon and within myelin sheaths, where they ... Together they form and compact myelin sheaths of nerve cells. Plaque proteins are molecules, that are required for the ... OAP-1/TSPAN-3 cooperates with β1-integrin and OSP/Claudin11 within myelin sheaths of oligodendrocytes, thereby affects the ...
WebMD explains myelin sheath, a sleeve that protects a part of your nerve cells, and how its related to multiple sclerosis. ... Myelin and Your Nerves. The myelin sheath wraps around the fibers that are the long threadlike part of a nerve cell. The sheath ... What Is a Myelin Sheath? Medically Reviewed by Melinda Ratini, MS, DO on August 20, 2021 ... Morell, P. "The Myelin Sheath." Basic Neurochemistry: Molecular, Cellular and Medical Aspects, Lippincott-Raven, 1999. ...
Albertas MYELIN SHEATHS have boldly thrust themselves forward and erupt here with an incredibly powerful debut 7-inch ... Like if someone plugged the entire C86 sound into a fried-out supergenerator, Myelin Sheaths have the potential to skyrocket ... Yet another Canadian entry in HoZacs new batch, Lethbridge (about 100 miles south of Calgary), Albertas MYELIN SHEATHS have ... Myelin Sheaths have found a perfect platform to desecrate the chill and melt the frozen wilderness around them. The endlessly ...
Similar words for Myelin Sheath. Definition: noun. [ˈʃiːθ] a protective covering (as for a knife or sword). ... Sentences with myelin-sheath 1. Noun Phrase So the damaged myelin sheath around the cochlear nerve neurons may cause the ... Vitamins B-6 and B-12 play a role in the production and maintenance of the myelin sheath around cells. 4. Noun Phrase The ... 4. myelin noun. [ˈmaɪɪlɪn] a white fatty substance that forms a medullary sheath around the axis cylinder of some nerve ...
... Myelination and Node of Ranvier Formation in a Human Motoneuron−Schwann Cell Serum-Free Coculture. June 8th, ... myelin sheath, node of Ranvier, T2910 News,Specialties Chemicals News Comments (0) ...
... the case for a lower resistance myelin sheath ... The resistances of node internode and myelin sheath were found ... Celio, M.R. 1976: The Schmidt-Lantermann incisures of the myelin sheath of Mauthner axons: site of longitudinal myelin growth ... Tuisku, F.; Hildebrand, C. 1992: Nodes of Ranvier and myelin sheath dimensions along exceptionally thin myelinated vertebrate ... The calculated lower resistance of the myelin sheath minimized the effective internodal time constant for a given nodal ...
... helps form tight junction structures that seal PNS myelin sheaths.Tight junction-like structures run along myelin sheaths in ... page 527) find evidence that these structures work as true tight junctions to seal off the myelin sheath and are required for ... Tight junction-like structures run along myelin sheaths in both the central and peripheral nervous systems (CNS and PNS), but ... This change in conductance properties indicated that, without claudin-19, the myelin sheath of Schwann cell appeared to be ...
Myelin sheath (#13598). Myelin sheath (#13598) Shown from perspective. Licence * Science License for academic purposes such as ...
Myelin is a fatty sheath that coats nerve cells. It consists of about 70% lipids. In the central nervous system, it is made of ... known as the Myelin Sheath. (Myelin sheath)-The Myelin Sheath is made up of a material called myelin, which is produced by ... Myelin Sheath Essay. The Myelin Sheath: Essential for Rapid Saltatory Conduction The synthesis and maintenance of the myelin ... A Look at Myelin and Myelin-Related Disorders Essay. A Look at Myelin and Myelin-Related Disorders Myelin is the protective ...
The inner mesaxon (Terminologia histologica: Mesaxon internum) is the connection between the myelin sheath and the inner part ... "The Myelin Sheath". Basic Neurochemistry: Molecular, Cellular and Medical Aspects. 6th edition. v t e (All stub articles, ... is the connection of the outer cell membrane to the compact myelin sheath. ...
Located in myelin sheath. Is expressed in ganglia and trigeminal nerve. Orthologous to human ACTR1A (actin related protein 1A ...
... defined as the ratio between the inner and the outer diameter of the myelin sheath, is a fundamental property of white matter ... that can be computed from a simple formula relating the myelin volume fraction to the fiber volume fraction or the axon volume ... The myelin g-ratio, defined as the ratio between the inner and the outer diameter of the myelin sheath, is a fundamental ... In vivo histology of the myelin g-ratio with magnetic resonance imaging Neuroimage. 2015 Sep:118:397-405. doi: 10.1016/j. ...
Myelin sheath injury Thallium accumulates in tissues with high potassium concentrations such as muscle, heart, and central and ... Although the exact mechanism of myelin injury by thallium is unknown, there are consistent findings of fragmentation and ... degeneration of myelin in both the central and peripheral nervous systems. A Wallerian degeneration pattern first develops in ...
... total 215 sheaths from 3 mice). Note that about 85% of the myelin sheath did not generate any Ca2+ event during the recording. ... f, Ca2+ events detected in e. g, Distribution of the Ca2+ event numbers detected in myelin sheaths within 6 minutes (n = ... 9 Myelinating oligodendrocytes exhibit Ca2+ events in only a select few myelin sheaths.. a, Local calcium events detected ( ... corresponds to local myelin sheath detected using SCoRe. Cyan arrowhead indicates auto-fluorescent vascular structures. ...
This is called the myelin sheath. MS can cause a wide range of symptoms, including issues with balance and coordination, ... As previously mentioned, MS causes damage to myelin. Current treatments for MS can reduce the severity of the disease, and slow ... However, they do not directly repair damaged myelin.. Researchers and doctors are now trying to form treatment strategies for ... NGF also regulates key structural proteins that can compromise myelin. NGF also promotes the production of another neurotrophin ...
GO:0043209-myelin sheath. −0.03. −3.09. −1.55. 0.30. ATP1A2 (ATPase Na+/K+ Transporting Sub-unit Alpha 2). P50993. 1.12. 1.55. ...
Dive into the research topics of Sulfatide, a major lipid component of myelin sheath, activates inflammatory responses as an ... Sulfatide, a major lipid component of myelin sheath, activates inflammatory responses as an endogenous stimulator in brain- ...
Dive into the research topics of Actin Filament Turnover Drives Leading Edge Growth during Myelin Sheath Formation in the ... Actin Filament Turnover Drives Leading Edge Growth during Myelin Sheath Formation in the Central Nervous System. ...
Myelin sheath around nerve cells contain lipids What role do these molecules play here Experts plzz answer fast I have test ... The insulated sheath that surrounds the core of the nerve fibre or the axon of the neuron is called myelin sheath. It consists ... Myelin sheath around nerve cells contain lipids . What role do these molecules play here?? Experts plzz answer fast I have test ...
Thin-layer chromatography and X-ray diffraction were used to analyze the lipid content/composition and the myelin structure of ... Myelin Sheath / metabolism * Myelin Sheath / pathology* * Optic Nerve / cytology* * Optic Nerve / pathology* ... Myelin abnormalities in the optic and sciatic nerves in mice with GM1-gangliosidosis ASN Neuro. 2015 Feb 18;7(1): ... The abnormalities in GM1 and myelin lipids in optic nerve of β-gal -/- mice correlated with a reduction in the relative amount ...
His research looks at neurons and the myelin sheath that surrounds them within the white matter of the brain. Myelin is an ... Zeroing in on the Myelin Sheath. Vitamin D Deficiency and Dementia. Spotlight on Current Research: Call for Participants. ... Manitoba Researcher Zeros in on the Myelin Sheath. Shenghua Zhu knows all too well the affects Alzheimers disease has on a ... "A breakdown in myelin results in abnormal thoughts and behaviours, and evidence suggests that Alzheimers disease may involve ...
MS is caused by damage to the myelin sheath. This sheath is the protective covering that surrounds nerve cells. When this nerve ...
This myelin sheath allows electrical impulses to transmit quickly and efficiently along the nerve cells. If myelin is damaged, ... Detailed explanation-2: -Schwann cells are the glial cells that form the myelin sheath on axons outside the brain. Unlike ... Detailed explanation-3: -Myelin is an insulating layer, or sheath that forms around nerves, including those in the brain and ... What do you call the neuroglial cells that form myelin sheaths around the nerve fibers of the CENTRAL NERVOUS SYSTEM? ...
The myelin sheath surrounds nerves and facilitates the transmission of impulses to the brain. Damage to the myelin sheath ... Demyelinating disorders: Listen [MP3]A medical condition in which the myelin sheath is damaged. ... A disease of the central nervous system characterized by the destruction of the myelin sheath surrounding neurons, resulting in ...
A Nanoscale Model System for the Human Myelin Sheath. Preprint. *May 2021 ... Research in this field is limited by the complex nature of native myelin and by difficulties in obtaining good in vitro model ... Here, we for the first time establish nanodiscs with the challenging lipid composition of myelin of the peripheral or central ...
Myelin Sheath = Blue to blue-black Background = Light tan. Weil Method. Reagents: Luxol Fast Blue, Lithium Carbonate, 70% ... Myelin Sheaths = Blue to green Axons and nerve fibers = Black. Luxol Fast Blue-Holmes Silver Nitrate Method. ... When an axon is severely or irreversibly injured, all of the axon distal to the injury disappears along with its myelin sheath ... Demonstration of myelin sheath. Weil Method, Luxol Fast Blue, Luxol Fast Blue-PAS-Hematoxylin. ...
Schwann cells produce myelin sheath around peripheral nerve axons. Myelination is critical for rapid propagation of action ...
One suspected protein is myelin-associated glycoprotein, found in the sheath of myelin that insulates axons. Another is ... Insulating myelin sheath also began to form along the fresh nerves. As a result, the rodents were once again able to use their ... but because of injury trauma and inflammation they have lost their myelin sheaths. Without the insulating layer the nerves no ... Cells called oligodendrocytes are responsible for producing myelin in the CNS. Neurobiologist Hans Keirstead of the University ...
B. Myelin sheath Explanation. The myelin sheath is a protective covering that surrounds the axon of neurons. It acts as an ... the myelin sheath degenerates, leading to a disruption in the communication between nerve cells. This loss of myelin can result ... Axons are typically long and covered by a myelin sheath, which helps to insulate and speed up the transmission of the ...
... a single myelin sheath separates into three distinct sets of myelin lamellae (numbered in the figure), each of which terminate ... A myelin sheath (*) from another cell overrides this paranodal region. c, Freeze-fracture replica showing a palisade of ... Defects were similar to those reported previously; compact myelin sheaths appeared to be normal in cross sections (data not ... Hildebrand C, Bowe CM, Remahl IN ( 1994) Myelination and myelin sheath remodelling in normal and pathological PNS nerve fibres ...
... this is called the myelin sheath. So Schwann cells make up the myelin sheath. Ill do one more just like that. And then these ... How does Myelin Sheath increase the transmission rate?. Answer. Button navigates to signup page. •. 4 comments. Comment on Boaz ... Maybe he was the guy who looked and saw they had these little slots here where you dont have myelin sheath. So these are the ... So these are called Schwann cells and theyre covering-- they make up the myelin sheath. So this covering, this insulation, at ...
  • It may also contribute to greater stability of the axon under conditions of prolonged depolarization, by allowing the internodal axolemma to be repolarized more rapidly by voltage dependent K+ currents and making the input resistance of the internode dependent on the permeability of its own axolemma, more than that of the surrounding myelin sheath. (eurekamag.com)
  • Oligodendrocytes and Schwann cells form myelin by wrapping around the axon. (bartleby.com)
  • The myelin g-ratio, defined as the ratio between the inner and the outer diameter of the myelin sheath, is a fundamental property of white matter that can be computed from a simple formula relating the myelin volume fraction to the fiber volume fraction or the axon volume fraction. (nih.gov)
  • In this paper, a unique combination of magnetization transfer, diffusion imaging and histology is presented, providing a novel method for in vivo magnetic resonance imaging of the axon volume fraction and the myelin g-ratio. (nih.gov)
  • Unlike oligodendrocytes, Schwann cells do not have multiple cellular extensions, but instead each cell engulfs a segment of axon and forms a multilayered myelin sheath around it (Figure 3). (github.io)
  • Each Schwann cell forms a single myelin sheath around an axon. (github.io)
  • Why doesn't Mylein Sheath completely cover the axon? (khanacademy.org)
  • Additionally, loss of myelin and/or oligodendrocytes can negatively influence signal transduction and axon integrity. (lu.se)
  • This electron micrograph shows a cross section through an axon, its myelin wrap, and the associated myelin-producing Schwann cell from the the cochlear nerve of the cat. (cellimagelibrary.org)
  • Other genetic defects affect the protective lining around the axon, called the myelin sheath. (hopkinsmedicine.org)
  • The myelin sheath may be compact and spiralling around the axon or it may be non-compact and form a simple envelope around the axon. (scirp.org)
  • This is not surprising given the strong evidence for interaction between myelin and axon gene expression in development and after experimental nerve lesions. (medscape.com)
  • Myelinating Schwann cells form a myelin sheath around a single axon and express high levels of myelin-related proteins and messenger RNA (mRNA). (medscape.com)
  • The sheath protects these fibers, known as axons, a lot like the insulation around an electrical wire. (webmd.com)
  • A Look at Myelin and Myelin-Related Disorders Myelin is the protective sheath around axons in the nervous system, and is often referred to as 'white matter. (bartleby.com)
  • central nervous system that has the potential to cause significant disability in those affected through the body's immune system attacking and destroying the myelin sheaths surrounding the axons. (bartleby.com)
  • The myelin sheath is where the nerve axons serve as an electrical insulator that speeds up nerve impulses to muscles and other effectors. (bartleby.com)
  • Multiple Sclerosis (MS) is a type of autoimmune disease in which the myelin sheath that covers axons and speeds up the transmission of nerve impulse in the brain is damaged or destroyed. (bartleby.com)
  • Schwann cells are the glial cells that form the myelin sheath on axons outside the brain. (github.io)
  • Schwann cells produce myelin sheath around peripheral nerve axons. (jci.org)
  • Nerves are made up of axons (nerve fibers) surrounded by a myelin sheath. (medicalnewstoday.com)
  • All axons (with very, very rare exceptions) are surrounded by a myelin sheath. (scirp.org)
  • Myelin is a substance that makes up the protective sheath (myelin sheath) that coats nerve fibers (axons). (nih.gov)
  • MS attacks axons in the central nervous system protected by myelin, which are commonly called white matter. (nih.gov)
  • On autopsy, swelling, vacuolation, and fragmentation of axons and myelin sheaths were observed in the spinal column and sciatic nerves. (cdc.gov)
  • Slender processes of NEURONS, including the AXONS and their glial envelopes (MYELIN SHEATH). (bvsalud.org)
  • page 527 ) find evidence that these structures work as true tight junctions to seal off the myelin sheath and are required for proper neural conductance in the Schwann cells of the PNS.Claudin proteins are major cell adhesion molecules in tight junctions. (rupress.org)
  • This change in conductance properties indicated that, without claudin-19, the myelin sheath of Schwann cell appeared to be inadequately sealed from the environment. (rupress.org)
  • In the peripheral nervous system, myelin is made of a Schwann cell. (bartleby.com)
  • The inner mesaxon (Terminologia histologica: Mesaxon internum) is the connection between the myelin sheath and the inner part of the cell membrane of the Schwann cell, which is directly opposite the axolemma, i.e. the cell membrane of the nerve fibre ensheathed by the Schwann cell. (wikipedia.org)
  • Schwann cells make myelin in the peripheral nervous system (PNS: nerves) and oligodendrocytes in the central nervous system (CNS: brain and spinal cord). (github.io)
  • Myelin is formed by Schwann cells in the peripheral nervous system (PNS) and oligodendrocytes in the central nervous system (CNS). (github.io)
  • Schwann cells form a thin cytoplasmic tube around each fiber and further wrap larger fibers in a multilayered insulating membrane (myelin sheath). (msdmanuals.com)
  • In the case of MS, the body attacks and destroys the protective sheath that surrounds your nerves. (pilatesfoundation.com)
  • An autopsy showed inflammation and erosion of the protective sheath known as myelin in two nerves, but no evidence of the Zika virus in nerve cells. (medscape.com)
  • When that happens, the nerves inside the sheath can be damaged. (webmd.com)
  • When the myelin sheath is damaged, nerves cannot conduct the electrical impulses efficiently. (bartleby.com)
  • By contrast, the relative amount of myelin and periodicity in the sciatic nerves from control and β-gal -/- mice were indistinguishable, suggesting minimal pathological involvement in sciatic nerve. (nih.gov)
  • Myelin is an insulating layer, or sheath that forms around nerves, including those in the brain and spinal cord. (github.io)
  • Damage to myelin disrupts the ability of nerves to transmit information to nerve cells, resulting in neurological disability. (medicalnewstoday.com)
  • It's caused by a breakdown of the protective cover (myelin sheath) around the nerves in the brain and spinal cord. (healthline.com)
  • Primary symptoms of MS are those that occur due to damage to the myelin sheath and the nerves within. (healthline.com)
  • As the immune system damages the myelin sheath, nerves are exposed. (healthline.com)
  • The damage to and destruction of the myelin eventually affects the nerves. (pilatesfoundation.com)
  • When your myelin coating is damaged, the nerves inside it can't properly send signals, and the exchange of information between your body and brain is disrupted. (thirdage.com)
  • When your myelin is damaged, the nerves inside it can't properly send signals, and the exchange of information between your body and brain is disrupted. (thirdage.com)
  • In MS, the immune system cells that normally protect us from viruses, bacteria, and unhealthy cells mistakenly attack myelin in the central nervous system (brain, optic nerves, and spinal cord). (nih.gov)
  • A demyelinating disease is any condition that causes damage to the protective covering (myelin sheath) that surrounds nerve fibers in your brain, the nerves leading to the eyes (optic nerves) and spinal cord. (mayoclinic.org)
  • MS occurs when the immune system attacks myelin, leaving scars or lesions in the demyelinated areas of the brain and spinal cord. (medicalnewstoday.com)
  • MS directly affects the nervous system as the body's immune cells attack myelin in the brain and spinal cord. (healthline.com)
  • The researchers found that, in mice lacking the neuregulin-1 gene, spontaneous myelin repair was completely prevented and spinal nerve fibres remained demyelinated (i.e. unable to send nerve signals along the spinal cord). (ox.ac.uk)
  • Myelin oligodendrocyte glycoprotein antibody-associated disease (MOGAD) - inflammatory disorder of the central nervous system, predominantly of the optic nerve and spinal cord. (mayoclinic.org)
  • These studies culminated in a thesis, presented in Lund in 1905, entitled "Uber Spinalgangliezellen und Markscheiden" (On spinal ganglion cells and myelin sheaths). (lu.se)
  • If you have multiple sclerosis (MS), a disease that causes your immune system to attack your central nervous system, your myelin sheaths can be damaged. (webmd.com)
  • Multiple sclerosis results from the progressive deterioration of the protective fatty myelin sheath surrounding nerve cells. (sciencedaily.com)
  • The term multiple sclerosis refers to the distinctive areas of scar tissue (sclerosis-also called plaques or lesions) that result from the attack on myelin by the immune system. (nih.gov)
  • We searched PubMed and Medline for studies published during the last 10 years with the general term "optic neuritis" and specific terms like "typical optic neuritis," "atypical optic neuritis," "multiple sclerosis," "neuromyelitis optic neuritis," and "myelin oligodendrocyte glycoprotein antibody. (lww.com)
  • Apoptotic oligodendrocytes, changes in the oligodendrocyte progenitor cell (OPC) population and loss of myelin were evaluated at 2, 7 and 21 days following TBI. (lu.se)
  • MS also causes the immune system to attack oligodendrocytes, the myelin-producing cells that would otherwise repair the damaged sheath. (thirdage.com)
  • 9 10 ] Recently published data from India suggests that 50% of NMOSD either have aquaporin4 (AQP4) or myelin oligodendrocytes (MOG) antibodies. (lww.com)
  • Sulfatide, a major lipid component of myelin sheath, activates inflammatory responses as an endogenous stimulator in brain-resident immune cells. (korea.ac.kr)
  • Dive into the research topics of 'Sulfatide, a major lipid component of myelin sheath, activates inflammatory responses as an endogenous stimulator in brain-resident immune cells. (korea.ac.kr)
  • GALC degrades galactosylceramide, a major component of myelin, and other terminal beta-galactose-containing sphingolipids, including psychosine (galactosylsphingosine). (medscape.com)
  • Myelin sheaths are sleeves of fatty tissue that protect your nerve cells. (webmd.com)
  • Myelin is a fatty sheath that coats nerve cells. (bartleby.com)
  • This sheath is the protective covering that surrounds nerve cells. (medlineplus.gov)
  • This myelin sheath allows electrical impulses to transmit quickly and efficiently along the nerve cells. (github.io)
  • It occurs when your immune system attacks the myelin sheath, a protective coating on your nerve cells. (thirdage.com)
  • The loss of myelin hinders nerve cells from communicating with one another, leading to a host of neurological symptoms including loss of sensation, muscle spasms and weakness, fatigue, and pain. (sciencedaily.com)
  • The myelin sheath contains a variety of fatty substances (lipids), and contains at least ten distinct chemicals (2). (bartleby.com)
  • Myelin is rich in lipids and proteins that form layers around the nerve fibers and acts as insulation and protection. (bartleby.com)
  • The abnormalities in GM1 and myelin lipids in optic nerve of β-gal -/- mice correlated with a reduction in the relative amount of myelin and periodicity in fresh nerve. (nih.gov)
  • Tight junction-like structures run along myelin sheaths in both the central and peripheral nervous systems (CNS and PNS), but have only been functionally characterized in the CNS. (rupress.org)
  • Myelin sheath insulates and covers the neurons intermittently, helping to speed up nerve signals. (medicinenet.com)
  • Much like the insulation around an electrical wire, the myelin sheath enables nerve signals (electrical impulses) to be conducted along the nerve fiber with speed and accuracy. (merckmanuals.com)
  • It attacks both the myelin and the cells that make it. (webmd.com)
  • In this disorder, your immune system attacks the myelin sheath or the cells that produce and maintain it. (mayoclinic.org)
  • NGF also regulates key structural proteins that can compromise myelin. (medicalnewstoday.com)
  • Myelin Proteins" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings) . (harvard.edu)
  • Proteins found in the myelin sheath. (harvard.edu)
  • This graph shows the total number of publications written about "Myelin Proteins" by people in Harvard Catalyst Profiles by year, and whether "Myelin Proteins" was a major or minor topic of these publication. (harvard.edu)
  • Below are the most recent publications written about "Myelin Proteins" by people in Profiles. (harvard.edu)
  • FEAST: A flow cytometry-based toolkit for interrogating microglial engulfment of synaptic and myelin proteins. (harvard.edu)
  • The Myelin Sheath: Essential for Rapid Saltatory Conduction The synthesis and maintenance of the myelin sheath is critical for normal neural function because myelination is responsible for the saltatory conduction of action potentials that significantly increases the conduction velocity of electrical signals (Bartzokis, 2004). (bartleby.com)
  • But if you have MS, your body's immune system treats myelin as a threat. (webmd.com)
  • A lot of the research into MS is focused on boosting your body's ability to repair damaged myelin. (webmd.com)
  • The damage of the myelin sheath is caused by inflammation of the brain, and may have significant damages to other areas as well. (bartleby.com)
  • As previously mentioned, MS causes damage to myelin. (medicalnewstoday.com)
  • MS is caused by damage to the myelin sheath. (medlineplus.gov)
  • Through mechanisms that at present can only be speculated about, myelin disturbances result in axonal damage. (medscape.com)
  • Balo's concentric sclerosis causes concentric rings of myelin destruction that can be seen on an MRI and is another variant type of MS that can progress rapidly. (nih.gov)
  • Psychosine also accumulates and is thought to be a highly cytotoxic substance and responsible for the widespread destruction of myelin-producing oligodendroglia. (medscape.com)
  • In this case, it looks like it was antibodies that led to destruction of that myelin sheath," said Sharp, whose study was published online December 13 in Emerging Infectious Diseases, the CDC's public health journal. (medscape.com)
  • This attack causes inflammation and injury to the nerve sheath and ultimately to the nerve fibers that it surrounds. (mayoclinic.org)
  • The outer mesaxon (Terminologia histologica: Mesaxon externum) is the connection of the outer cell membrane to the compact myelin sheath. (wikipedia.org)
  • Coronal section of rat brain triple-labeled with fluoromyelin (green), DiI (red), and TO-PRO3 (blue) which stain for myelin, blood vessels, and cell bodies, respectively. (cellimagelibrary.org)
  • This myelin sheath is crucial for efficient communication between the brain and the body. (ox.ac.uk)
  • Most nerve fibers inside and outside the brain are wrapped with many layers of tissue composed of a fat (lipoprotein) called myelin. (merckmanuals.com)
  • The myelin sheath is like insulation on a wire. (thirdage.com)
  • This conduction is indeed very different and faster than for fibres "without" myelin. (scirp.org)
  • Our results indicate that TBI induces oligodendrocyte apoptosis and widespread myelin loss, followed by a concomitant increase in the number of OPCs. (lu.se)
  • The resistances of node internode and myelin sheath were found to produce suitable length and time constants and prolonged afterpotentials, when inserted into the model. (eurekamag.com)
  • The problem of minimizing the internodal time constant was met in the conventional model through the low parallel resistance of the node, while in the new model it was met by reducing the resistance of the myelin sheath. (eurekamag.com)
  • Developing myelin specific promoters for schwannoma gene therapy. (harvard.edu)
  • [ 6 ] However, the gene mutations responsible for the different forms of CMT1 are clearly myelin genes. (medscape.com)
  • An essential biosynthetic function of animal peroxisomes is to catalyze the first reactions in the formation of plasmalogens , which are the most abundant class of phospholipids in myelin ( Figure 12-32 ). (nih.gov)
  • Peak synthesis and turnover of galactosylceramide coincides with the peak period of myelin formation and turnover during the first 18 months of life. (medscape.com)
  • However, because of deficient GALC activity (0-5% reference value), galactosylceramide accumulation occurs, particularly during the early period of rapid myelin turnover. (medscape.com)
  • The word Multiple refers to many areas and Sclerosis refers to the scar of the myelin sheath. (bartleby.com)
  • What do you call the neuroglial cells that form myelin sheaths around the nerve fibers of the CENTRAL NERVOUS SYSTEM? (github.io)
  • The myelin sheath wraps around the fibers that are the long threadlike part of a nerve cell. (webmd.com)
  • A nerve is an organ composed of multiple nerve fibers bound together by sheaths of connective tissue. (medscape.com)
  • Claudin-19 (green) helps form tight junction structures that seal PNS myelin sheaths. (rupress.org)
  • Researchers and doctors are now trying to form treatment strategies for MS that include neurotrophins, such as NGF, for myelin repair. (medicalnewstoday.com)
  • These layers form the myelin sheath. (merckmanuals.com)
  • Protein citrullination marks myelin protein aggregation and disease progression in mouse ALS models. (harvard.edu)
  • When the myelin sheath is healthy, nerve signals are sent and received quickly. (webmd.com)
  • 1. Myelin are important parts of the nervous system, they are "capable of responding to experiences for learning and long-term behavioral capacity" (Myelinate). (bartleby.com)
  • MS is also categorized as an autoimmune disease in which the immune system instigates an immune response upon encountering the specific myelin antigen and therefore initiating a constant degradation of the myelin sheath. (bartleby.com)
  • In Krabbe disease, myelin composition is not qualitatively abnormal. (medscape.com)
  • Accumulation of β-amyloid precursor protein was observed in white matter tracts in both models in areas with preserved and reduced myelin staining. (lu.se)