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Vav2 catalysis-dependent pathways contribute to skeletal muscle growth and metabolic homeostasis
Skeletal muscle promotes metabolic balance by regulating glucose uptake and the stimulation of multiple interorgan crosstalk. We show here that the catalytic activity of Vav2, a Rho GTPase activator, modulates the signaling output of the IGF1- and insulin-stimulated phosphatidylinositol 3-kinase pat...
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/PMC7669868/ https://www.ncbi.nlm.nih.gov/pubmed/33199701 http://dx.doi.org/10.1038/s41467-020-19489-z |
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author | Rodríguez-Fdez, Sonia Lorenzo-Martín, L. Francisco Fernández-Pisonero, Isabel Porteiro, Begoña Veyrat-Durebex, Christelle Beiroa, Daniel Al-Massadi, Omar Abad, Antonio Diéguez, Carlos Coppari, Roberto Nogueiras, Rubén Bustelo, Xosé R. |
author_facet | Rodríguez-Fdez, Sonia Lorenzo-Martín, L. Francisco Fernández-Pisonero, Isabel Porteiro, Begoña Veyrat-Durebex, Christelle Beiroa, Daniel Al-Massadi, Omar Abad, Antonio Diéguez, Carlos Coppari, Roberto Nogueiras, Rubén Bustelo, Xosé R. |
author_sort | Rodríguez-Fdez, Sonia |
collection | PubMed |
description | Skeletal muscle promotes metabolic balance by regulating glucose uptake and the stimulation of multiple interorgan crosstalk. We show here that the catalytic activity of Vav2, a Rho GTPase activator, modulates the signaling output of the IGF1- and insulin-stimulated phosphatidylinositol 3-kinase pathway in that tissue. Consistent with this, mice bearing a Vav2 protein with decreased catalytic activity exhibit reduced muscle mass, lack of proper insulin responsiveness and, at much later times, a metabolic syndrome-like condition. Conversely, mice expressing a catalytically hyperactive Vav2 develop muscle hypertrophy and increased insulin responsiveness. Of note, while hypoactive Vav2 predisposes to, hyperactive Vav2 protects against high fat diet-induced metabolic imbalance. These data unveil a regulatory layer affecting the signaling output of insulin family factors in muscle. |
format | Online Article Text |
id | pubmed-7669868 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-76698682020-11-24 Vav2 catalysis-dependent pathways contribute to skeletal muscle growth and metabolic homeostasis Rodríguez-Fdez, Sonia Lorenzo-Martín, L. Francisco Fernández-Pisonero, Isabel Porteiro, Begoña Veyrat-Durebex, Christelle Beiroa, Daniel Al-Massadi, Omar Abad, Antonio Diéguez, Carlos Coppari, Roberto Nogueiras, Rubén Bustelo, Xosé R. Nat Commun Article Skeletal muscle promotes metabolic balance by regulating glucose uptake and the stimulation of multiple interorgan crosstalk. We show here that the catalytic activity of Vav2, a Rho GTPase activator, modulates the signaling output of the IGF1- and insulin-stimulated phosphatidylinositol 3-kinase pathway in that tissue. Consistent with this, mice bearing a Vav2 protein with decreased catalytic activity exhibit reduced muscle mass, lack of proper insulin responsiveness and, at much later times, a metabolic syndrome-like condition. Conversely, mice expressing a catalytically hyperactive Vav2 develop muscle hypertrophy and increased insulin responsiveness. Of note, while hypoactive Vav2 predisposes to, hyperactive Vav2 protects against high fat diet-induced metabolic imbalance. These data unveil a regulatory layer affecting the signaling output of insulin family factors in muscle. Nature Publishing Group UK 2020-11-16 /pmc/articles/PMC7669868/ /pubmed/33199701 http://dx.doi.org/10.1038/s41467-020-19489-z 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 Rodríguez-Fdez, Sonia Lorenzo-Martín, L. Francisco Fernández-Pisonero, Isabel Porteiro, Begoña Veyrat-Durebex, Christelle Beiroa, Daniel Al-Massadi, Omar Abad, Antonio Diéguez, Carlos Coppari, Roberto Nogueiras, Rubén Bustelo, Xosé R. Vav2 catalysis-dependent pathways contribute to skeletal muscle growth and metabolic homeostasis |
title | Vav2 catalysis-dependent pathways contribute to skeletal muscle growth and metabolic homeostasis |
title_full | Vav2 catalysis-dependent pathways contribute to skeletal muscle growth and metabolic homeostasis |
title_fullStr | Vav2 catalysis-dependent pathways contribute to skeletal muscle growth and metabolic homeostasis |
title_full_unstemmed | Vav2 catalysis-dependent pathways contribute to skeletal muscle growth and metabolic homeostasis |
title_short | Vav2 catalysis-dependent pathways contribute to skeletal muscle growth and metabolic homeostasis |
title_sort | vav2 catalysis-dependent pathways contribute to skeletal muscle growth and metabolic homeostasis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7669868/ https://www.ncbi.nlm.nih.gov/pubmed/33199701 http://dx.doi.org/10.1038/s41467-020-19489-z |
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