Myelin Repair: From Animal Models to Humans

It is widely thought that brain repair does not occur, but myelin regeneration provides clear evidence to the contrary. Spontaneous remyelination may occur after injury or in multiple sclerosis (MS). However, the efficiency of remyelination varies considerably between MS patients and between the les...

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Main Authors: Myriam Cayre, Marie Falque, Océane Mercier, Karine Magalon, Pascale Durbec
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-04-01
Series:Frontiers in Cellular Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fncel.2021.604865/full
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spelling doaj-fbcccca0baa041e8972cea4d3d95f2232021-04-14T04:47:12ZengFrontiers Media S.A.Frontiers in Cellular Neuroscience1662-51022021-04-011510.3389/fncel.2021.604865604865Myelin Repair: From Animal Models to HumansMyriam CayreMarie FalqueOcéane MercierKarine MagalonPascale DurbecIt is widely thought that brain repair does not occur, but myelin regeneration provides clear evidence to the contrary. Spontaneous remyelination may occur after injury or in multiple sclerosis (MS). However, the efficiency of remyelination varies considerably between MS patients and between the lesions of each patient. Myelin repair is essential for optimal functional recovery, so a profound understanding of the cells and mechanisms involved in this process is required for the development of new therapeutic strategies. In this review, we describe how animal models and modern cell tracing and imaging methods have helped to identify the cell types involved in myelin regeneration. In addition to the oligodendrocyte progenitor cells identified in the 1990s as the principal source of remyelinating cells in the central nervous system (CNS), other cell populations, including subventricular zone-derived neural progenitors, Schwann cells, and even spared mature oligodendrocytes, have more recently emerged as potential contributors to CNS remyelination. We will also highlight the conditions known to limit endogenous repair, such as aging, chronic inflammation, and the production of extracellular matrix proteins, and the role of astrocytes and microglia in these processes. Finally, we will present the discrepancies between observations in humans and in rodents, discussing the relationship of findings in experimental models to myelin repair in humans. These considerations are particularly important from a therapeutic standpoint.https://www.frontiersin.org/articles/10.3389/fncel.2021.604865/fullmyelin repairoligodendrocyteneural stem cellssubventricular zonemultiple sclerosistherapeutic strategies
collection DOAJ
language English
format Article
sources DOAJ
author Myriam Cayre
Marie Falque
Océane Mercier
Karine Magalon
Pascale Durbec
spellingShingle Myriam Cayre
Marie Falque
Océane Mercier
Karine Magalon
Pascale Durbec
Myelin Repair: From Animal Models to Humans
Frontiers in Cellular Neuroscience
myelin repair
oligodendrocyte
neural stem cells
subventricular zone
multiple sclerosis
therapeutic strategies
author_facet Myriam Cayre
Marie Falque
Océane Mercier
Karine Magalon
Pascale Durbec
author_sort Myriam Cayre
title Myelin Repair: From Animal Models to Humans
title_short Myelin Repair: From Animal Models to Humans
title_full Myelin Repair: From Animal Models to Humans
title_fullStr Myelin Repair: From Animal Models to Humans
title_full_unstemmed Myelin Repair: From Animal Models to Humans
title_sort myelin repair: from animal models to humans
publisher Frontiers Media S.A.
series Frontiers in Cellular Neuroscience
issn 1662-5102
publishDate 2021-04-01
description It is widely thought that brain repair does not occur, but myelin regeneration provides clear evidence to the contrary. Spontaneous remyelination may occur after injury or in multiple sclerosis (MS). However, the efficiency of remyelination varies considerably between MS patients and between the lesions of each patient. Myelin repair is essential for optimal functional recovery, so a profound understanding of the cells and mechanisms involved in this process is required for the development of new therapeutic strategies. In this review, we describe how animal models and modern cell tracing and imaging methods have helped to identify the cell types involved in myelin regeneration. In addition to the oligodendrocyte progenitor cells identified in the 1990s as the principal source of remyelinating cells in the central nervous system (CNS), other cell populations, including subventricular zone-derived neural progenitors, Schwann cells, and even spared mature oligodendrocytes, have more recently emerged as potential contributors to CNS remyelination. We will also highlight the conditions known to limit endogenous repair, such as aging, chronic inflammation, and the production of extracellular matrix proteins, and the role of astrocytes and microglia in these processes. Finally, we will present the discrepancies between observations in humans and in rodents, discussing the relationship of findings in experimental models to myelin repair in humans. These considerations are particularly important from a therapeutic standpoint.
topic myelin repair
oligodendrocyte
neural stem cells
subventricular zone
multiple sclerosis
therapeutic strategies
url https://www.frontiersin.org/articles/10.3389/fncel.2021.604865/full
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