Author
Listed:
- Sonia Rodríguez-Fdez
(CSIC-University of Salamanca
CSIC-University of Salamanca
CSIC-University of Salamanca)
- L. Francisco Lorenzo-Martín
(CSIC-University of Salamanca
CSIC-University of Salamanca
CSIC-University of Salamanca)
- Isabel Fernández-Pisonero
(CSIC-University of Salamanca
CSIC-University of Salamanca
CSIC-University of Salamanca)
- Begoña Porteiro
(University of Santiago de Compostela
University of Santiago de Compostela)
- Christelle Veyrat-Durebex
(University of Geneva)
- Daniel Beiroa
(University of Santiago de Compostela
University of Santiago de Compostela)
- Omar Al-Massadi
(University of Santiago de Compostela
University of Santiago de Compostela
Centro de Investigación Biomédica en Red de Fisiopatología de la Obesidad y Nutrición (CIBEROBN), University of Santiago de Compostela)
- Antonio Abad
(CSIC-University of Salamanca
CSIC-University of Salamanca
CSIC-University of Salamanca)
- Carlos Diéguez
(University of Santiago de Compostela
University of Santiago de Compostela
Centro de Investigación Biomédica en Red de Fisiopatología de la Obesidad y Nutrición (CIBEROBN), University of Santiago de Compostela)
- Roberto Coppari
(University of Geneva
University of Geneva)
- Rubén Nogueiras
(University of Santiago de Compostela
University of Santiago de Compostela
Centro de Investigación Biomédica en Red de Fisiopatología de la Obesidad y Nutrición (CIBEROBN), University of Santiago de Compostela)
- Xosé R. Bustelo
(CSIC-University of Salamanca
CSIC-University of Salamanca
CSIC-University of Salamanca)
Abstract
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.
Suggested Citation
Sonia Rodríguez-Fdez & L. Francisco Lorenzo-Martín & Isabel Fernández-Pisonero & Begoña Porteiro & Christelle Veyrat-Durebex & Daniel Beiroa & Omar Al-Massadi & Antonio Abad & Carlos Diéguez & Roberto, 2020.
"Vav2 catalysis-dependent pathways contribute to skeletal muscle growth and metabolic homeostasis,"
Nature Communications, Nature, vol. 11(1), pages 1-26, December.
Handle:
RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-19489-z
DOI: 10.1038/s41467-020-19489-z
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