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Activin A more prominently regulates muscle mass in primates than does GDF8

Authors :
Jason Mastaitis
Andrew J. Murphy
Jesus A. Trejos
Stephen Jaspers
Jeffrey Pangilinan
Trevor Stitt
Erqian Na
Esther Latres
Yu Bai
George D. Yancopoulos
Lawrence Miloscio
Jesper Gromada
Ashique Rafique
Wen Fury
Jee Hae Kim
Tobias Willer
Katie Cavino
Haruka Okamoto
Angelos Papatheodorou
Source :
Nature Communications, Nature Communications, Vol 8, Iss 1, Pp 1-13 (2017)
Publication Year :
2017
Publisher :
Springer Science and Business Media LLC, 2017.

Abstract

Growth and differentiation factor 8 (GDF8) is a TGF-β superfamily member, and negative regulator of skeletal muscle mass. GDF8 inhibition results in prominent muscle growth in mice, but less impressive hypertrophy in primates, including man. Broad TGF-β inhibition suggests another family member negatively regulates muscle mass, and its blockade enhances muscle growth seen with GDF8-specific inhibition. Here we show that activin A is the long-sought second negative muscle regulator. Activin A specific inhibition, on top of GDF8 inhibition, leads to pronounced muscle hypertrophy and force production in mice and monkeys. Inhibition of these two ligands mimics the hypertrophy seen with broad TGF-β blockers, while avoiding the adverse effects due to inhibition of multiple family members. Altogether, we identify activin A as a second negative regulator of muscle mass, and suggest that inhibition of both ligands provides a preferred therapeutic approach, which maximizes the benefit:risk ratio for muscle diseases in man.<br />Inhibition of GDF8 increases muscle mass in mice, but is less effective in monkeys and humans. Here the authors show that activin A also inhibits muscle hypertrophy and that concomitant inhibition of activin A and GDF8 synergistically increases muscle mass in mice and non-human primates.

Details

ISSN :
20411723
Volume :
8
Database :
OpenAIRE
Journal :
Nature Communications
Accession number :
edsair.doi.dedup.....87739244226941d93603a7a609426820
Full Text :
https://doi.org/10.1038/ncomms15153