Myostatin up-regulation is associated with the skeletal muscle response to hypoxic stimuli.

Hayot, Maurice;Rodriguez, Julie;Vernus, Barbara;Carnac, Gilles;Bonnieu, Anne;et.al.
(2011) Molecular and Cellular Endocrinology — Vol. 332, n° 1-2, p. 38-47 (2011)

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Authors
  • Hayot, Maurice
    Author
  • Rodriguez, JulieUCLouvain
    Author
  • Vernus, Barbara
    Author
  • Carnac, Gilles
    Author
  • Bonnieu, Anne
    Author
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Abstract
Myostatin and hypoxia signalling pathways are able to induce skeletal muscle atrophy, but whether a relationship between these two pathways exists is currently unknown. Here, we tested the hypothesis that a potential mechanism for hypoxia effect on skeletal muscle may be through regulation of myostatin. We reported an induction of myostatin expression in muscles of rats exposed to chronic hypoxia. Interestingly, we also demonstrated increased skeletal muscle myostatin protein expression in skeletal muscle of hypoxemic patients with severe chronic obstructive pulmonary disease (COPD). Parallel studies in human skeletal muscle cell cultures showed that induction of myostatin expression in myotubes treated with hypoxia-mimicking agent such as cobalt chloride (CoCl(2)) is associated with myotube atrophy. Furthermore, we demonstrated that inhibition of myostatin by means of genetic deletion of myostatin or treatment with blocking antimyostatin antibodies inhibits the CoCl(2)-induced atrophy in muscle cells. Finally, addition of recombinant myostatin restored the CoCl(2)-induced atrophy in myostatin deficient myotubes. These results strongly suggest that myostatin can play an essential role in the adaptation of skeletal muscle to hypoxic environment.
Affiliations
  • Université MontpellierInstitut National de la Recherche Agronomique (INRA)

Citations

Hayot, M., Rodriguez, J., Vernus, B., Carnac, G., Jean, E., Allen, D., Goret, L., Obert, P., Candau, R., & Bonnieu, A. (2011). Myostatin up-regulation is associated with the skeletal muscle response to hypoxic stimuli. Molecular and Cellular Endocrinology, 332(1-2), 38-47. https://doi.org/10.1016/j.mce.2010.09.008 (Original work published 2011)