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Sestrins are evolutionarily conserved mediators of exercise benefits
Exercise is among the most effective interventions for age-associated mobility decline and metabolic dysregulation. Although long-term endurance exercise promotes insulin sensitivity and expands respiratory capacity, genetic components and pathways mediating the metabolic benefits of exercise have r...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6955242/ https://www.ncbi.nlm.nih.gov/pubmed/31929512 http://dx.doi.org/10.1038/s41467-019-13442-5 |
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author | Kim, Myungjin Sujkowski, Alyson Namkoong, Sim Gu, Bondong Cobb, Tyler Kim, Boyoung Kowalsky, Allison H. Cho, Chun-Seok Semple, Ian Ro, Seung-Hyun Davis, Carol Brooks, Susan V. Karin, Michael Wessells, Robert J. Lee, Jun Hee |
author_facet | Kim, Myungjin Sujkowski, Alyson Namkoong, Sim Gu, Bondong Cobb, Tyler Kim, Boyoung Kowalsky, Allison H. Cho, Chun-Seok Semple, Ian Ro, Seung-Hyun Davis, Carol Brooks, Susan V. Karin, Michael Wessells, Robert J. Lee, Jun Hee |
author_sort | Kim, Myungjin |
collection | PubMed |
description | Exercise is among the most effective interventions for age-associated mobility decline and metabolic dysregulation. Although long-term endurance exercise promotes insulin sensitivity and expands respiratory capacity, genetic components and pathways mediating the metabolic benefits of exercise have remained elusive. Here, we show that Sestrins, a family of evolutionarily conserved exercise-inducible proteins, are critical mediators of exercise benefits. In both fly and mouse models, genetic ablation of Sestrins prevents organisms from acquiring metabolic benefits of exercise and improving their endurance through training. Conversely, Sestrin upregulation mimics both molecular and physiological effects of exercise, suggesting that it could be a major effector of exercise metabolism. Among the various targets modulated by Sestrin in response to exercise, AKT and PGC1α are critical for the Sestrin effects in extending endurance. These results indicate that Sestrin is a key integrating factor that drives the benefits of chronic exercise to metabolism and physical endurance. |
format | Online Article Text |
id | pubmed-6955242 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69552422020-01-13 Sestrins are evolutionarily conserved mediators of exercise benefits Kim, Myungjin Sujkowski, Alyson Namkoong, Sim Gu, Bondong Cobb, Tyler Kim, Boyoung Kowalsky, Allison H. Cho, Chun-Seok Semple, Ian Ro, Seung-Hyun Davis, Carol Brooks, Susan V. Karin, Michael Wessells, Robert J. Lee, Jun Hee Nat Commun Article Exercise is among the most effective interventions for age-associated mobility decline and metabolic dysregulation. Although long-term endurance exercise promotes insulin sensitivity and expands respiratory capacity, genetic components and pathways mediating the metabolic benefits of exercise have remained elusive. Here, we show that Sestrins, a family of evolutionarily conserved exercise-inducible proteins, are critical mediators of exercise benefits. In both fly and mouse models, genetic ablation of Sestrins prevents organisms from acquiring metabolic benefits of exercise and improving their endurance through training. Conversely, Sestrin upregulation mimics both molecular and physiological effects of exercise, suggesting that it could be a major effector of exercise metabolism. Among the various targets modulated by Sestrin in response to exercise, AKT and PGC1α are critical for the Sestrin effects in extending endurance. These results indicate that Sestrin is a key integrating factor that drives the benefits of chronic exercise to metabolism and physical endurance. Nature Publishing Group UK 2020-01-13 /pmc/articles/PMC6955242/ /pubmed/31929512 http://dx.doi.org/10.1038/s41467-019-13442-5 Text en © The Author(s) 2020 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/. |
spellingShingle | Article Kim, Myungjin Sujkowski, Alyson Namkoong, Sim Gu, Bondong Cobb, Tyler Kim, Boyoung Kowalsky, Allison H. Cho, Chun-Seok Semple, Ian Ro, Seung-Hyun Davis, Carol Brooks, Susan V. Karin, Michael Wessells, Robert J. Lee, Jun Hee Sestrins are evolutionarily conserved mediators of exercise benefits |
title | Sestrins are evolutionarily conserved mediators of exercise benefits |
title_full | Sestrins are evolutionarily conserved mediators of exercise benefits |
title_fullStr | Sestrins are evolutionarily conserved mediators of exercise benefits |
title_full_unstemmed | Sestrins are evolutionarily conserved mediators of exercise benefits |
title_short | Sestrins are evolutionarily conserved mediators of exercise benefits |
title_sort | sestrins are evolutionarily conserved mediators of exercise benefits |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6955242/ https://www.ncbi.nlm.nih.gov/pubmed/31929512 http://dx.doi.org/10.1038/s41467-019-13442-5 |
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