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Star power: harnessing the reactive astrocyte response to promote remyelination in multiple sclerosis

Astrocytes are indispensable for central nervous system development and homeostasis. In response to injury and disease, astrocytes are integral to the immunological- and the, albeit limited, repair response. In this review, we will examine some of the functions reactive astrocytes play in the contex...

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Autores principales: Junior, Markley Silva Oliveira, Reiche, Laura, Daniele, Emerson, Kortebi, Ines, Faiz, Maryam, Küry, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581572/
https://www.ncbi.nlm.nih.gov/pubmed/37721287
http://dx.doi.org/10.4103/1673-5374.380879
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author Junior, Markley Silva Oliveira
Reiche, Laura
Daniele, Emerson
Kortebi, Ines
Faiz, Maryam
Küry, Patrick
author_facet Junior, Markley Silva Oliveira
Reiche, Laura
Daniele, Emerson
Kortebi, Ines
Faiz, Maryam
Küry, Patrick
author_sort Junior, Markley Silva Oliveira
collection PubMed
description Astrocytes are indispensable for central nervous system development and homeostasis. In response to injury and disease, astrocytes are integral to the immunological- and the, albeit limited, repair response. In this review, we will examine some of the functions reactive astrocytes play in the context of multiple sclerosis and related animal models. We will consider the heterogeneity or plasticity of astrocytes and the mechanisms by which they promote or mitigate demyelination. Finally, we will discuss a set of biomedical strategies that can stimulate astrocytes in their promyelinating response.
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spelling pubmed-105815722023-10-18 Star power: harnessing the reactive astrocyte response to promote remyelination in multiple sclerosis Junior, Markley Silva Oliveira Reiche, Laura Daniele, Emerson Kortebi, Ines Faiz, Maryam Küry, Patrick Neural Regen Res Review Astrocytes are indispensable for central nervous system development and homeostasis. In response to injury and disease, astrocytes are integral to the immunological- and the, albeit limited, repair response. In this review, we will examine some of the functions reactive astrocytes play in the context of multiple sclerosis and related animal models. We will consider the heterogeneity or plasticity of astrocytes and the mechanisms by which they promote or mitigate demyelination. Finally, we will discuss a set of biomedical strategies that can stimulate astrocytes in their promyelinating response. Wolters Kluwer - Medknow 2023-07-20 /pmc/articles/PMC10581572/ /pubmed/37721287 http://dx.doi.org/10.4103/1673-5374.380879 Text en Copyright: © Neural Regeneration Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Review
Junior, Markley Silva Oliveira
Reiche, Laura
Daniele, Emerson
Kortebi, Ines
Faiz, Maryam
Küry, Patrick
Star power: harnessing the reactive astrocyte response to promote remyelination in multiple sclerosis
title Star power: harnessing the reactive astrocyte response to promote remyelination in multiple sclerosis
title_full Star power: harnessing the reactive astrocyte response to promote remyelination in multiple sclerosis
title_fullStr Star power: harnessing the reactive astrocyte response to promote remyelination in multiple sclerosis
title_full_unstemmed Star power: harnessing the reactive astrocyte response to promote remyelination in multiple sclerosis
title_short Star power: harnessing the reactive astrocyte response to promote remyelination in multiple sclerosis
title_sort star power: harnessing the reactive astrocyte response to promote remyelination in multiple sclerosis
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10581572/
https://www.ncbi.nlm.nih.gov/pubmed/37721287
http://dx.doi.org/10.4103/1673-5374.380879
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