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Regulatory roles of mitochondria and metabolism in neurogenesis

Neural stem cells (NSCs) undergo massive molecular and cellular changes during neuronal differentiation. These include mitochondria and metabolism remodelling, which were thought to be mostly permissive cues, but recent work indicates that they are causally linked to neurogenesis. Striking remodelli...

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Detalles Bibliográficos
Autores principales: Iwata, Ryohei, Vanderhaeghen, Pierre
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Current Biology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8415079/
https://www.ncbi.nlm.nih.gov/pubmed/34171617
http://dx.doi.org/10.1016/j.conb.2021.05.003
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author Iwata, Ryohei
Vanderhaeghen, Pierre
author_facet Iwata, Ryohei
Vanderhaeghen, Pierre
author_sort Iwata, Ryohei
collection PubMed
description Neural stem cells (NSCs) undergo massive molecular and cellular changes during neuronal differentiation. These include mitochondria and metabolism remodelling, which were thought to be mostly permissive cues, but recent work indicates that they are causally linked to neurogenesis. Striking remodelling of mitochondria occurs right after mitosis of NSCs, which influences the postmitotic daughter cells towards self-renewal or differentiation. The transitioning to neuronal fate requires metabolic rewiring including increased oxidative phosphorylation activity, which drives transcriptional and epigenetic effects to influence cell fate. Mitochondria metabolic pathways also contribute in an essential way to the regulation of NSC proliferation and self-renewal. The influence of mitochondria and metabolism on neurogenesis is conserved from fly to human systems, but also displays striking differences linked to cell context or species. These new findings have important implications for our understanding of neurodevelopmental diseases and possibly human brain evolution.
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spelling pubmed-84150792021-09-08 Regulatory roles of mitochondria and metabolism in neurogenesis Iwata, Ryohei Vanderhaeghen, Pierre Curr Opin Neurobiol Article Neural stem cells (NSCs) undergo massive molecular and cellular changes during neuronal differentiation. These include mitochondria and metabolism remodelling, which were thought to be mostly permissive cues, but recent work indicates that they are causally linked to neurogenesis. Striking remodelling of mitochondria occurs right after mitosis of NSCs, which influences the postmitotic daughter cells towards self-renewal or differentiation. The transitioning to neuronal fate requires metabolic rewiring including increased oxidative phosphorylation activity, which drives transcriptional and epigenetic effects to influence cell fate. Mitochondria metabolic pathways also contribute in an essential way to the regulation of NSC proliferation and self-renewal. The influence of mitochondria and metabolism on neurogenesis is conserved from fly to human systems, but also displays striking differences linked to cell context or species. These new findings have important implications for our understanding of neurodevelopmental diseases and possibly human brain evolution. Current Biology 2021-08 /pmc/articles/PMC8415079/ /pubmed/34171617 http://dx.doi.org/10.1016/j.conb.2021.05.003 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Iwata, Ryohei
Vanderhaeghen, Pierre
Regulatory roles of mitochondria and metabolism in neurogenesis
title Regulatory roles of mitochondria and metabolism in neurogenesis
title_full Regulatory roles of mitochondria and metabolism in neurogenesis
title_fullStr Regulatory roles of mitochondria and metabolism in neurogenesis
title_full_unstemmed Regulatory roles of mitochondria and metabolism in neurogenesis
title_short Regulatory roles of mitochondria and metabolism in neurogenesis
title_sort regulatory roles of mitochondria and metabolism in neurogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8415079/
https://www.ncbi.nlm.nih.gov/pubmed/34171617
http://dx.doi.org/10.1016/j.conb.2021.05.003
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