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Endurance exercise training-responsive miR-19b-3p improves skeletal muscle glucose metabolism

Skeletal muscle is a highly adaptable tissue and remodels in response to exercise training. Using short RNA sequencing, we determine the miRNA profile of skeletal muscle from healthy male volunteers before and after a 14-day aerobic exercise training regime. Among the exercise training-responsive mi...

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Autores principales: Massart, Julie, Sjögren, Rasmus J. O., Egan, Brendan, Garde, Christian, Lindgren, Magnus, Gu, Weifeng, Ferreira, Duarte M. S., Katayama, Mutsumi, Ruas, Jorge L., Barrès, Romain, O’Gorman, Donal J., Zierath, Juleen R., Krook, Anna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8511155/
https://www.ncbi.nlm.nih.gov/pubmed/34642330
http://dx.doi.org/10.1038/s41467-021-26095-0
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author Massart, Julie
Sjögren, Rasmus J. O.
Egan, Brendan
Garde, Christian
Lindgren, Magnus
Gu, Weifeng
Ferreira, Duarte M. S.
Katayama, Mutsumi
Ruas, Jorge L.
Barrès, Romain
O’Gorman, Donal J.
Zierath, Juleen R.
Krook, Anna
author_facet Massart, Julie
Sjögren, Rasmus J. O.
Egan, Brendan
Garde, Christian
Lindgren, Magnus
Gu, Weifeng
Ferreira, Duarte M. S.
Katayama, Mutsumi
Ruas, Jorge L.
Barrès, Romain
O’Gorman, Donal J.
Zierath, Juleen R.
Krook, Anna
author_sort Massart, Julie
collection PubMed
description Skeletal muscle is a highly adaptable tissue and remodels in response to exercise training. Using short RNA sequencing, we determine the miRNA profile of skeletal muscle from healthy male volunteers before and after a 14-day aerobic exercise training regime. Among the exercise training-responsive miRNAs identified, miR-19b-3p was selected for further validation. Overexpression of miR-19b-3p in human skeletal muscle cells increases insulin signaling, glucose uptake, and maximal oxygen consumption, recapitulating the adaptive response to aerobic exercise training. Overexpression of miR-19b-3p in mouse flexor digitorum brevis muscle enhances contraction-induced glucose uptake, indicating that miR-19b-3p exerts control on exercise training-induced adaptations in skeletal muscle. Potential targets of miR-19b-3p that are reduced after aerobic exercise training include KIF13A, MAPK6, RNF11, and VPS37A. Amongst these, RNF11 silencing potentiates glucose uptake in human skeletal muscle cells. Collectively, we identify miR-19b-3p as an aerobic exercise training-induced miRNA that regulates skeletal muscle glucose metabolism.
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spelling pubmed-85111552021-10-29 Endurance exercise training-responsive miR-19b-3p improves skeletal muscle glucose metabolism Massart, Julie Sjögren, Rasmus J. O. Egan, Brendan Garde, Christian Lindgren, Magnus Gu, Weifeng Ferreira, Duarte M. S. Katayama, Mutsumi Ruas, Jorge L. Barrès, Romain O’Gorman, Donal J. Zierath, Juleen R. Krook, Anna Nat Commun Article Skeletal muscle is a highly adaptable tissue and remodels in response to exercise training. Using short RNA sequencing, we determine the miRNA profile of skeletal muscle from healthy male volunteers before and after a 14-day aerobic exercise training regime. Among the exercise training-responsive miRNAs identified, miR-19b-3p was selected for further validation. Overexpression of miR-19b-3p in human skeletal muscle cells increases insulin signaling, glucose uptake, and maximal oxygen consumption, recapitulating the adaptive response to aerobic exercise training. Overexpression of miR-19b-3p in mouse flexor digitorum brevis muscle enhances contraction-induced glucose uptake, indicating that miR-19b-3p exerts control on exercise training-induced adaptations in skeletal muscle. Potential targets of miR-19b-3p that are reduced after aerobic exercise training include KIF13A, MAPK6, RNF11, and VPS37A. Amongst these, RNF11 silencing potentiates glucose uptake in human skeletal muscle cells. Collectively, we identify miR-19b-3p as an aerobic exercise training-induced miRNA that regulates skeletal muscle glucose metabolism. Nature Publishing Group UK 2021-10-12 /pmc/articles/PMC8511155/ /pubmed/34642330 http://dx.doi.org/10.1038/s41467-021-26095-0 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Massart, Julie
Sjögren, Rasmus J. O.
Egan, Brendan
Garde, Christian
Lindgren, Magnus
Gu, Weifeng
Ferreira, Duarte M. S.
Katayama, Mutsumi
Ruas, Jorge L.
Barrès, Romain
O’Gorman, Donal J.
Zierath, Juleen R.
Krook, Anna
Endurance exercise training-responsive miR-19b-3p improves skeletal muscle glucose metabolism
title Endurance exercise training-responsive miR-19b-3p improves skeletal muscle glucose metabolism
title_full Endurance exercise training-responsive miR-19b-3p improves skeletal muscle glucose metabolism
title_fullStr Endurance exercise training-responsive miR-19b-3p improves skeletal muscle glucose metabolism
title_full_unstemmed Endurance exercise training-responsive miR-19b-3p improves skeletal muscle glucose metabolism
title_short Endurance exercise training-responsive miR-19b-3p improves skeletal muscle glucose metabolism
title_sort endurance exercise training-responsive mir-19b-3p improves skeletal muscle glucose metabolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8511155/
https://www.ncbi.nlm.nih.gov/pubmed/34642330
http://dx.doi.org/10.1038/s41467-021-26095-0
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