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Transforming growth factor‐beta renders ageing microglia inhibitory to oligodendrocyte generation by CNS progenitors
It is now well‐established that the macrophage and microglial response to CNS demyelination influences remyelination by removing myelin debris and secreting a variety of signaling molecules that influence the behaviour of oligodendrocyte progenitor cells (OPCs). Previous studies have shown that chan...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563458/ https://www.ncbi.nlm.nih.gov/pubmed/30861188 http://dx.doi.org/10.1002/glia.23612 |
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author | Baror, Roey Neumann, Björn Segel, Michael Chalut, Kevin J. Fancy, Stephen P. J. Schafer, Dorothy P. Franklin, Robin J. M. |
author_facet | Baror, Roey Neumann, Björn Segel, Michael Chalut, Kevin J. Fancy, Stephen P. J. Schafer, Dorothy P. Franklin, Robin J. M. |
author_sort | Baror, Roey |
collection | PubMed |
description | It is now well‐established that the macrophage and microglial response to CNS demyelination influences remyelination by removing myelin debris and secreting a variety of signaling molecules that influence the behaviour of oligodendrocyte progenitor cells (OPCs). Previous studies have shown that changes in microglia contribute to the age‐related decline in the efficiency of remyelination. In this study, we show that microglia increase their expression of the proteoglycan NG2 with age, and that this is associated with an altered micro‐niche generated by aged, but not young, microglia that can divert the differentiation OPCs from oligodendrocytes into astrocytes in vitro. We further show that these changes in ageing microglia are generated by exposure to high levels of TGFβ. Thus, our findings suggest that the rising levels of circulating TGFβ known to occur with ageing contribute to the age‐related decline in remyelination by impairing the ability of microglia to promote oligodendrocyte differentiation from OPCs, and therefore could be a potential therapeutic target to promote remyelination. |
format | Online Article Text |
id | pubmed-6563458 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65634582019-06-17 Transforming growth factor‐beta renders ageing microglia inhibitory to oligodendrocyte generation by CNS progenitors Baror, Roey Neumann, Björn Segel, Michael Chalut, Kevin J. Fancy, Stephen P. J. Schafer, Dorothy P. Franklin, Robin J. M. Glia Research Articles It is now well‐established that the macrophage and microglial response to CNS demyelination influences remyelination by removing myelin debris and secreting a variety of signaling molecules that influence the behaviour of oligodendrocyte progenitor cells (OPCs). Previous studies have shown that changes in microglia contribute to the age‐related decline in the efficiency of remyelination. In this study, we show that microglia increase their expression of the proteoglycan NG2 with age, and that this is associated with an altered micro‐niche generated by aged, but not young, microglia that can divert the differentiation OPCs from oligodendrocytes into astrocytes in vitro. We further show that these changes in ageing microglia are generated by exposure to high levels of TGFβ. Thus, our findings suggest that the rising levels of circulating TGFβ known to occur with ageing contribute to the age‐related decline in remyelination by impairing the ability of microglia to promote oligodendrocyte differentiation from OPCs, and therefore could be a potential therapeutic target to promote remyelination. John Wiley & Sons, Inc. 2019-03-12 2019-07 /pmc/articles/PMC6563458/ /pubmed/30861188 http://dx.doi.org/10.1002/glia.23612 Text en © 2019 The Authors. Glia published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Baror, Roey Neumann, Björn Segel, Michael Chalut, Kevin J. Fancy, Stephen P. J. Schafer, Dorothy P. Franklin, Robin J. M. Transforming growth factor‐beta renders ageing microglia inhibitory to oligodendrocyte generation by CNS progenitors |
title | Transforming growth factor‐beta renders ageing microglia inhibitory to oligodendrocyte generation by CNS progenitors |
title_full | Transforming growth factor‐beta renders ageing microglia inhibitory to oligodendrocyte generation by CNS progenitors |
title_fullStr | Transforming growth factor‐beta renders ageing microglia inhibitory to oligodendrocyte generation by CNS progenitors |
title_full_unstemmed | Transforming growth factor‐beta renders ageing microglia inhibitory to oligodendrocyte generation by CNS progenitors |
title_short | Transforming growth factor‐beta renders ageing microglia inhibitory to oligodendrocyte generation by CNS progenitors |
title_sort | transforming growth factor‐beta renders ageing microglia inhibitory to oligodendrocyte generation by cns progenitors |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6563458/ https://www.ncbi.nlm.nih.gov/pubmed/30861188 http://dx.doi.org/10.1002/glia.23612 |
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