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Vav2 catalysis-dependent pathways contribute to skeletal muscle growth and metabolic homeostasis

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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