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Astrocytes and Microglia as Major Players of Myelin Production in Normal and Pathological Conditions
Myelination is an essential process that consists of the ensheathment of axons by myelin. In the central nervous system (CNS), myelin is synthesized by oligodendrocytes. The proliferation, migration, and differentiation of oligodendrocyte precursor cells constitute a prerequisite before mature oligo...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155218/ https://www.ncbi.nlm.nih.gov/pubmed/32317939 http://dx.doi.org/10.3389/fncel.2020.00079 |
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author | Traiffort, Elisabeth Kassoussi, Abdelmoumen Zahaf, Amina Laouarem, Yousra |
author_facet | Traiffort, Elisabeth Kassoussi, Abdelmoumen Zahaf, Amina Laouarem, Yousra |
author_sort | Traiffort, Elisabeth |
collection | PubMed |
description | Myelination is an essential process that consists of the ensheathment of axons by myelin. In the central nervous system (CNS), myelin is synthesized by oligodendrocytes. The proliferation, migration, and differentiation of oligodendrocyte precursor cells constitute a prerequisite before mature oligodendrocytes extend their processes around the axons and progressively generate a multilamellar lipidic sheath. Although myelination is predominately driven by oligodendrocytes, the other glial cells including astrocytes and microglia, also contribute to this process. The present review is an update of the most recent emerging mechanisms involving astrocyte and microglia in myelin production. The contribution of these cells will be first described during developmental myelination that occurs in the early postnatal period and is critical for the proper development of cognition and behavior. Then, we will report the novel findings regarding the beneficial or deleterious effects of astroglia and microglia, which respectively promote or impair the endogenous capacity of oligodendrocyte progenitor cells (OPCs) to induce spontaneous remyelination after myelin loss. Acute delineation of astrocyte and microglia activities and cross-talk should uncover the way towards novel therapeutic perspectives aimed at recovering proper myelination during development or at breaking down the barriers impeding the regeneration of the damaged myelin that occurs in CNS demyelinating diseases. |
format | Online Article Text |
id | pubmed-7155218 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71552182020-04-21 Astrocytes and Microglia as Major Players of Myelin Production in Normal and Pathological Conditions Traiffort, Elisabeth Kassoussi, Abdelmoumen Zahaf, Amina Laouarem, Yousra Front Cell Neurosci Cellular Neuroscience Myelination is an essential process that consists of the ensheathment of axons by myelin. In the central nervous system (CNS), myelin is synthesized by oligodendrocytes. The proliferation, migration, and differentiation of oligodendrocyte precursor cells constitute a prerequisite before mature oligodendrocytes extend their processes around the axons and progressively generate a multilamellar lipidic sheath. Although myelination is predominately driven by oligodendrocytes, the other glial cells including astrocytes and microglia, also contribute to this process. The present review is an update of the most recent emerging mechanisms involving astrocyte and microglia in myelin production. The contribution of these cells will be first described during developmental myelination that occurs in the early postnatal period and is critical for the proper development of cognition and behavior. Then, we will report the novel findings regarding the beneficial or deleterious effects of astroglia and microglia, which respectively promote or impair the endogenous capacity of oligodendrocyte progenitor cells (OPCs) to induce spontaneous remyelination after myelin loss. Acute delineation of astrocyte and microglia activities and cross-talk should uncover the way towards novel therapeutic perspectives aimed at recovering proper myelination during development or at breaking down the barriers impeding the regeneration of the damaged myelin that occurs in CNS demyelinating diseases. Frontiers Media S.A. 2020-04-07 /pmc/articles/PMC7155218/ /pubmed/32317939 http://dx.doi.org/10.3389/fncel.2020.00079 Text en Copyright © 2020 Traiffort, Kassoussi, Zahaf and Laouarem. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Cellular Neuroscience Traiffort, Elisabeth Kassoussi, Abdelmoumen Zahaf, Amina Laouarem, Yousra Astrocytes and Microglia as Major Players of Myelin Production in Normal and Pathological Conditions |
title | Astrocytes and Microglia as Major Players of Myelin Production in Normal and Pathological Conditions |
title_full | Astrocytes and Microglia as Major Players of Myelin Production in Normal and Pathological Conditions |
title_fullStr | Astrocytes and Microglia as Major Players of Myelin Production in Normal and Pathological Conditions |
title_full_unstemmed | Astrocytes and Microglia as Major Players of Myelin Production in Normal and Pathological Conditions |
title_short | Astrocytes and Microglia as Major Players of Myelin Production in Normal and Pathological Conditions |
title_sort | astrocytes and microglia as major players of myelin production in normal and pathological conditions |
topic | Cellular Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7155218/ https://www.ncbi.nlm.nih.gov/pubmed/32317939 http://dx.doi.org/10.3389/fncel.2020.00079 |
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