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Extensive transcriptional and chromatin changes underlie astrocyte maturation in vivo and in culture
Astrocytes have essential functions in brain homeostasis that are established late in differentiation, but the mechanisms underlying the functional maturation of astrocytes are not well understood. Here we identify extensive transcriptional changes that occur during murine astrocyte maturation in vi...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282848/ https://www.ncbi.nlm.nih.gov/pubmed/34267208 http://dx.doi.org/10.1038/s41467-021-24624-5 |
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author | Lattke, Michael Goldstone, Robert Ellis, James K. Boeing, Stefan Jurado-Arjona, Jerónimo Marichal, Nicolás MacRae, James I. Berninger, Benedikt Guillemot, Francois |
author_facet | Lattke, Michael Goldstone, Robert Ellis, James K. Boeing, Stefan Jurado-Arjona, Jerónimo Marichal, Nicolás MacRae, James I. Berninger, Benedikt Guillemot, Francois |
author_sort | Lattke, Michael |
collection | PubMed |
description | Astrocytes have essential functions in brain homeostasis that are established late in differentiation, but the mechanisms underlying the functional maturation of astrocytes are not well understood. Here we identify extensive transcriptional changes that occur during murine astrocyte maturation in vivo that are accompanied by chromatin remodelling at enhancer elements. Investigating astrocyte maturation in a cell culture model revealed that in vitro-differentiated astrocytes lack expression of many mature astrocyte-specific genes, including genes for the transcription factors Rorb, Dbx2, Lhx2 and Fezf2. Forced expression of these factors in vitro induces distinct sets of mature astrocyte-specific transcripts. Culturing astrocytes in a three-dimensional matrix containing FGF2 induces expression of Rorb, Dbx2 and Lhx2 and improves astrocyte maturity based on transcriptional and chromatin profiles. Therefore, extrinsic signals orchestrate the expression of multiple intrinsic regulators, which in turn induce in a modular manner the transcriptional and chromatin changes underlying astrocyte maturation. |
format | Online Article Text |
id | pubmed-8282848 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-82828482021-07-23 Extensive transcriptional and chromatin changes underlie astrocyte maturation in vivo and in culture Lattke, Michael Goldstone, Robert Ellis, James K. Boeing, Stefan Jurado-Arjona, Jerónimo Marichal, Nicolás MacRae, James I. Berninger, Benedikt Guillemot, Francois Nat Commun Article Astrocytes have essential functions in brain homeostasis that are established late in differentiation, but the mechanisms underlying the functional maturation of astrocytes are not well understood. Here we identify extensive transcriptional changes that occur during murine astrocyte maturation in vivo that are accompanied by chromatin remodelling at enhancer elements. Investigating astrocyte maturation in a cell culture model revealed that in vitro-differentiated astrocytes lack expression of many mature astrocyte-specific genes, including genes for the transcription factors Rorb, Dbx2, Lhx2 and Fezf2. Forced expression of these factors in vitro induces distinct sets of mature astrocyte-specific transcripts. Culturing astrocytes in a three-dimensional matrix containing FGF2 induces expression of Rorb, Dbx2 and Lhx2 and improves astrocyte maturity based on transcriptional and chromatin profiles. Therefore, extrinsic signals orchestrate the expression of multiple intrinsic regulators, which in turn induce in a modular manner the transcriptional and chromatin changes underlying astrocyte maturation. Nature Publishing Group UK 2021-07-15 /pmc/articles/PMC8282848/ /pubmed/34267208 http://dx.doi.org/10.1038/s41467-021-24624-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Lattke, Michael Goldstone, Robert Ellis, James K. Boeing, Stefan Jurado-Arjona, Jerónimo Marichal, Nicolás MacRae, James I. Berninger, Benedikt Guillemot, Francois Extensive transcriptional and chromatin changes underlie astrocyte maturation in vivo and in culture |
title | Extensive transcriptional and chromatin changes underlie astrocyte maturation in vivo and in culture |
title_full | Extensive transcriptional and chromatin changes underlie astrocyte maturation in vivo and in culture |
title_fullStr | Extensive transcriptional and chromatin changes underlie astrocyte maturation in vivo and in culture |
title_full_unstemmed | Extensive transcriptional and chromatin changes underlie astrocyte maturation in vivo and in culture |
title_short | Extensive transcriptional and chromatin changes underlie astrocyte maturation in vivo and in culture |
title_sort | extensive transcriptional and chromatin changes underlie astrocyte maturation in vivo and in culture |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8282848/ https://www.ncbi.nlm.nih.gov/pubmed/34267208 http://dx.doi.org/10.1038/s41467-021-24624-5 |
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