Myelin: Difference between revisions

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'''Myelin''' is the [[lipid]] [[substance]] that covers long [[axon]]s to speed up [[action potential]]s, and is responsible for the appearance of the [[white matter]]. A myelinated axon consists of [[nodes of ranvier]], which are supported by [[glial cell]]s in the white matter and look like small [[tube]]s covering the axon with small gaps in between them. Myelin is created by [[oligodendrocytes]] in the [[central nervous system]], and by [[schwann cells]] in the [[peripheral nervous system]].
'''Myelin''' is the [[lipid]] [[substance]] that covers long axons to speed up [[action potential]]s, and is responsible for the appearance of the [[white matter]]. A myelinated axon consists of [[nodes of ranvier]], which are supported by [[glial cell]]s in the white matter and look like small [[tube]]s covering the axon with small gaps in between them. Myelin is created by [[oligodendrocytes]] in the [[central nervous system]], and by [[schwann cells]] in the [[peripheral nervous system]].
 
[[Demyelinating disease]], such as [[multiple sclerosis]], are characterized by loss of myelin. Genetic diseases involving a defect of the coding for [[peripheral nerve myelin protein 22]], such as [[Charcot-Marie-Tooth disease]], also display abnormal myelin.[[Category:Suggestion Bot Tag]]

Latest revision as of 06:01, 22 September 2024

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Myelin is the lipid substance that covers long axons to speed up action potentials, and is responsible for the appearance of the white matter. A myelinated axon consists of nodes of ranvier, which are supported by glial cells in the white matter and look like small tubes covering the axon with small gaps in between them. Myelin is created by oligodendrocytes in the central nervous system, and by schwann cells in the peripheral nervous system.

Demyelinating disease, such as multiple sclerosis, are characterized by loss of myelin. Genetic diseases involving a defect of the coding for peripheral nerve myelin protein 22, such as Charcot-Marie-Tooth disease, also display abnormal myelin.