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Genetic, Epigenetic, and Metabolic Maintenance of Neural Stem Cells During Aging

Tight metabolic regulation is essential to maintain stem cell homeostasis and support healthy aging. With age, metabolic alterations cause neural stem cell (NSC) dysfunction and are associated with a decline in neurogenesis, but the underlying mechanisms are not known. Aged stem cells display defect...

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Autor principal: Webb, Ashley
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7742972/
http://dx.doi.org/10.1093/geroni/igaa057.2664
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author Webb, Ashley
author_facet Webb, Ashley
author_sort Webb, Ashley
collection PubMed
description Tight metabolic regulation is essential to maintain stem cell homeostasis and support healthy aging. With age, metabolic alterations cause neural stem cell (NSC) dysfunction and are associated with a decline in neurogenesis, but the underlying mechanisms are not known. Aged stem cells display defects in the autophagy-lysosomal pathway that may disrupt mitochondrial dynamics, resulting in metabolic disruptions that alter self-renewal and differentiation potential. We have used genomic and functional approaches to investigate the metabolic mechanisms that support NSCs throughout aging. We found that mitochondrial and mitophagy gene networks as well as mitophagy dynamics are differentially regulated between the quiescent and activated states and become dysregulated with age. This work provides new insight into the metabolic regulation of NSCs and may lead to strategies to enhance neurogenesis in the context of aging and neurodegenerative disease.
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spelling pubmed-77429722020-12-21 Genetic, Epigenetic, and Metabolic Maintenance of Neural Stem Cells During Aging Webb, Ashley Innov Aging Abstracts Tight metabolic regulation is essential to maintain stem cell homeostasis and support healthy aging. With age, metabolic alterations cause neural stem cell (NSC) dysfunction and are associated with a decline in neurogenesis, but the underlying mechanisms are not known. Aged stem cells display defects in the autophagy-lysosomal pathway that may disrupt mitochondrial dynamics, resulting in metabolic disruptions that alter self-renewal and differentiation potential. We have used genomic and functional approaches to investigate the metabolic mechanisms that support NSCs throughout aging. We found that mitochondrial and mitophagy gene networks as well as mitophagy dynamics are differentially regulated between the quiescent and activated states and become dysregulated with age. This work provides new insight into the metabolic regulation of NSCs and may lead to strategies to enhance neurogenesis in the context of aging and neurodegenerative disease. Oxford University Press 2020-12-16 /pmc/articles/PMC7742972/ http://dx.doi.org/10.1093/geroni/igaa057.2664 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of The Gerontological Society of America. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstracts
Webb, Ashley
Genetic, Epigenetic, and Metabolic Maintenance of Neural Stem Cells During Aging
title Genetic, Epigenetic, and Metabolic Maintenance of Neural Stem Cells During Aging
title_full Genetic, Epigenetic, and Metabolic Maintenance of Neural Stem Cells During Aging
title_fullStr Genetic, Epigenetic, and Metabolic Maintenance of Neural Stem Cells During Aging
title_full_unstemmed Genetic, Epigenetic, and Metabolic Maintenance of Neural Stem Cells During Aging
title_short Genetic, Epigenetic, and Metabolic Maintenance of Neural Stem Cells During Aging
title_sort genetic, epigenetic, and metabolic maintenance of neural stem cells during aging
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7742972/
http://dx.doi.org/10.1093/geroni/igaa057.2664
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