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Epigenetic alterations in stem cell ageing—a promising target for age-reversing interventions?

Ageing is accompanied by loss of tissue integrity and organismal homeostasis partly due to decline in stem cell function. The age-associated decrease in stem cell abundance and activity is often referred to as stem cell exhaustion and is considered one major hallmark of ageing. Importantly, stem cel...

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Detalles Bibliográficos
Autores principales: Pouikli, Andromachi, Tessarz, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789308/
https://www.ncbi.nlm.nih.gov/pubmed/33738480
http://dx.doi.org/10.1093/bfgp/elab010
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author Pouikli, Andromachi
Tessarz, Peter
author_facet Pouikli, Andromachi
Tessarz, Peter
author_sort Pouikli, Andromachi
collection PubMed
description Ageing is accompanied by loss of tissue integrity and organismal homeostasis partly due to decline in stem cell function. The age-associated decrease in stem cell abundance and activity is often referred to as stem cell exhaustion and is considered one major hallmark of ageing. Importantly, stem cell proliferation and differentiation potential are tightly coupled to the cellular epigenetic state. Thus, research during the last years has started to investigate how the epigenome regulates stem cell function upon ageing. Here, we summarize the role of epigenetic regulation in stem cell fate decisions and we review the impact of age-related changes of the epigenome on stem cell activity. Finally, we discuss how targeted interventions on the epigenetic landscape might delay ageing and extend health-span.
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spelling pubmed-87893082022-01-26 Epigenetic alterations in stem cell ageing—a promising target for age-reversing interventions? Pouikli, Andromachi Tessarz, Peter Brief Funct Genomics Review Paper Ageing is accompanied by loss of tissue integrity and organismal homeostasis partly due to decline in stem cell function. The age-associated decrease in stem cell abundance and activity is often referred to as stem cell exhaustion and is considered one major hallmark of ageing. Importantly, stem cell proliferation and differentiation potential are tightly coupled to the cellular epigenetic state. Thus, research during the last years has started to investigate how the epigenome regulates stem cell function upon ageing. Here, we summarize the role of epigenetic regulation in stem cell fate decisions and we review the impact of age-related changes of the epigenome on stem cell activity. Finally, we discuss how targeted interventions on the epigenetic landscape might delay ageing and extend health-span. Oxford University Press 2021-03-19 /pmc/articles/PMC8789308/ /pubmed/33738480 http://dx.doi.org/10.1093/bfgp/elab010 Text en © The Author(s) 2021. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Paper
Pouikli, Andromachi
Tessarz, Peter
Epigenetic alterations in stem cell ageing—a promising target for age-reversing interventions?
title Epigenetic alterations in stem cell ageing—a promising target for age-reversing interventions?
title_full Epigenetic alterations in stem cell ageing—a promising target for age-reversing interventions?
title_fullStr Epigenetic alterations in stem cell ageing—a promising target for age-reversing interventions?
title_full_unstemmed Epigenetic alterations in stem cell ageing—a promising target for age-reversing interventions?
title_short Epigenetic alterations in stem cell ageing—a promising target for age-reversing interventions?
title_sort epigenetic alterations in stem cell ageing—a promising target for age-reversing interventions?
topic Review Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789308/
https://www.ncbi.nlm.nih.gov/pubmed/33738480
http://dx.doi.org/10.1093/bfgp/elab010
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