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Ageing, metabolism and the intestine

The intestinal epithelium serves as a dynamic barrier to the environment and integrates a variety of signals, including those from metabolites, commensal microbiota, immune responses and stressors upon ageing. The intestine is constantly challenged and requires a high renewal rate to replace damaged...

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Detalles Bibliográficos
Autores principales: Funk, Maja C, Zhou, Jun, Boutros, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332987/
https://www.ncbi.nlm.nih.gov/pubmed/32567155
http://dx.doi.org/10.15252/embr.202050047
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author Funk, Maja C
Zhou, Jun
Boutros, Michael
author_facet Funk, Maja C
Zhou, Jun
Boutros, Michael
author_sort Funk, Maja C
collection PubMed
description The intestinal epithelium serves as a dynamic barrier to the environment and integrates a variety of signals, including those from metabolites, commensal microbiota, immune responses and stressors upon ageing. The intestine is constantly challenged and requires a high renewal rate to replace damaged cells in order to maintain its barrier function. Essential for its renewal capacity are intestinal stem cells, which constantly give rise to progenitor cells that differentiate into the multiple cell types present in the epithelium. Here, we review the current state of research of how metabolism and ageing control intestinal stem cell function and epithelial homeostasis. We focus on recent insights gained from model organisms that indicate how changes in metabolic signalling during ageing are a major driver for the loss of stem cell plasticity and epithelial homeostasis, ultimately affecting the resilience of an organism and limiting its lifespan. We compare findings made in mouse and Drosophila and discuss differences and commonalities in the underlying signalling pathways and mechanisms in the context of ageing.
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spelling pubmed-73329872020-07-07 Ageing, metabolism and the intestine Funk, Maja C Zhou, Jun Boutros, Michael EMBO Rep Review The intestinal epithelium serves as a dynamic barrier to the environment and integrates a variety of signals, including those from metabolites, commensal microbiota, immune responses and stressors upon ageing. The intestine is constantly challenged and requires a high renewal rate to replace damaged cells in order to maintain its barrier function. Essential for its renewal capacity are intestinal stem cells, which constantly give rise to progenitor cells that differentiate into the multiple cell types present in the epithelium. Here, we review the current state of research of how metabolism and ageing control intestinal stem cell function and epithelial homeostasis. We focus on recent insights gained from model organisms that indicate how changes in metabolic signalling during ageing are a major driver for the loss of stem cell plasticity and epithelial homeostasis, ultimately affecting the resilience of an organism and limiting its lifespan. We compare findings made in mouse and Drosophila and discuss differences and commonalities in the underlying signalling pathways and mechanisms in the context of ageing. John Wiley and Sons Inc. 2020-06-21 2020-07-03 /pmc/articles/PMC7332987/ /pubmed/32567155 http://dx.doi.org/10.15252/embr.202050047 Text en © 2020 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Funk, Maja C
Zhou, Jun
Boutros, Michael
Ageing, metabolism and the intestine
title Ageing, metabolism and the intestine
title_full Ageing, metabolism and the intestine
title_fullStr Ageing, metabolism and the intestine
title_full_unstemmed Ageing, metabolism and the intestine
title_short Ageing, metabolism and the intestine
title_sort ageing, metabolism and the intestine
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7332987/
https://www.ncbi.nlm.nih.gov/pubmed/32567155
http://dx.doi.org/10.15252/embr.202050047
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