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Macroglial diversity: white and grey areas and relevance to remyelination

Macroglia, comprising astrocytes and oligodendroglial lineage cells, have long been regarded as uniform cell types of the central nervous system (CNS). Although regional morphological differences between these cell types were initially described after their identification a century ago, these differ...

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Autores principales: Werkman, Inge L., Lentferink, Dennis H., Baron, Wia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867526/
https://www.ncbi.nlm.nih.gov/pubmed/32648004
http://dx.doi.org/10.1007/s00018-020-03586-9
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author Werkman, Inge L.
Lentferink, Dennis H.
Baron, Wia
author_facet Werkman, Inge L.
Lentferink, Dennis H.
Baron, Wia
author_sort Werkman, Inge L.
collection PubMed
description Macroglia, comprising astrocytes and oligodendroglial lineage cells, have long been regarded as uniform cell types of the central nervous system (CNS). Although regional morphological differences between these cell types were initially described after their identification a century ago, these differences were largely ignored. Recently, accumulating evidence suggests that macroglial cells form distinct populations throughout the CNS, based on both functional and morphological features. Moreover, with the use of refined techniques including single-cell and single-nucleus RNA sequencing, additional evidence is emerging for regional macroglial heterogeneity at the transcriptional level. In parallel, several studies revealed the existence of regional differences in remyelination capacity between CNS grey and white matter areas, both in experimental models for successful remyelination as well as in the chronic demyelinating disease multiple sclerosis (MS). In this review, we provide an overview of the diversity in oligodendroglial lineage cells and astrocytes from the grey and white matter, as well as their interplay in health and upon demyelination and successful remyelination. In addition, we discuss the implications of regional macroglial diversity for remyelination in light of its failure in MS. Since the etiology of MS remains unknown and only disease-modifying treatments altering the immune response are available for MS, the elucidation of macroglial diversity in grey and white matter and its putative contribution to the observed difference in remyelination efficiency between these regions may open therapeutic avenues aimed at enhancing endogenous remyelination in either area.
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spelling pubmed-78675262021-02-16 Macroglial diversity: white and grey areas and relevance to remyelination Werkman, Inge L. Lentferink, Dennis H. Baron, Wia Cell Mol Life Sci Review Macroglia, comprising astrocytes and oligodendroglial lineage cells, have long been regarded as uniform cell types of the central nervous system (CNS). Although regional morphological differences between these cell types were initially described after their identification a century ago, these differences were largely ignored. Recently, accumulating evidence suggests that macroglial cells form distinct populations throughout the CNS, based on both functional and morphological features. Moreover, with the use of refined techniques including single-cell and single-nucleus RNA sequencing, additional evidence is emerging for regional macroglial heterogeneity at the transcriptional level. In parallel, several studies revealed the existence of regional differences in remyelination capacity between CNS grey and white matter areas, both in experimental models for successful remyelination as well as in the chronic demyelinating disease multiple sclerosis (MS). In this review, we provide an overview of the diversity in oligodendroglial lineage cells and astrocytes from the grey and white matter, as well as their interplay in health and upon demyelination and successful remyelination. In addition, we discuss the implications of regional macroglial diversity for remyelination in light of its failure in MS. Since the etiology of MS remains unknown and only disease-modifying treatments altering the immune response are available for MS, the elucidation of macroglial diversity in grey and white matter and its putative contribution to the observed difference in remyelination efficiency between these regions may open therapeutic avenues aimed at enhancing endogenous remyelination in either area. Springer International Publishing 2020-07-09 2021 /pmc/articles/PMC7867526/ /pubmed/32648004 http://dx.doi.org/10.1007/s00018-020-03586-9 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Review
Werkman, Inge L.
Lentferink, Dennis H.
Baron, Wia
Macroglial diversity: white and grey areas and relevance to remyelination
title Macroglial diversity: white and grey areas and relevance to remyelination
title_full Macroglial diversity: white and grey areas and relevance to remyelination
title_fullStr Macroglial diversity: white and grey areas and relevance to remyelination
title_full_unstemmed Macroglial diversity: white and grey areas and relevance to remyelination
title_short Macroglial diversity: white and grey areas and relevance to remyelination
title_sort macroglial diversity: white and grey areas and relevance to remyelination
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867526/
https://www.ncbi.nlm.nih.gov/pubmed/32648004
http://dx.doi.org/10.1007/s00018-020-03586-9
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