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Activin A more prominently regulates muscle mass in primates than does GDF8
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 nega...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5414365/ https://www.ncbi.nlm.nih.gov/pubmed/28452368 http://dx.doi.org/10.1038/ncomms15153 |
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author | Latres, Esther Mastaitis, Jason Fury, Wen Miloscio, Lawrence Trejos, Jesus Pangilinan, Jeffrey Okamoto, Haruka Cavino, Katie Na, Erqian Papatheodorou, Angelos Willer, Tobias Bai, Yu Hae Kim, Jee Rafique, Ashique Jaspers, Stephen Stitt, Trevor Murphy, Andrew J. Yancopoulos, George D. Gromada, Jesper |
author_facet | Latres, Esther Mastaitis, Jason Fury, Wen Miloscio, Lawrence Trejos, Jesus Pangilinan, Jeffrey Okamoto, Haruka Cavino, Katie Na, Erqian Papatheodorou, Angelos Willer, Tobias Bai, Yu Hae Kim, Jee Rafique, Ashique Jaspers, Stephen Stitt, Trevor Murphy, Andrew J. Yancopoulos, George D. Gromada, Jesper |
author_sort | Latres, Esther |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-5414365 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-54143652017-05-17 Activin A more prominently regulates muscle mass in primates than does GDF8 Latres, Esther Mastaitis, Jason Fury, Wen Miloscio, Lawrence Trejos, Jesus Pangilinan, Jeffrey Okamoto, Haruka Cavino, Katie Na, Erqian Papatheodorou, Angelos Willer, Tobias Bai, Yu Hae Kim, Jee Rafique, Ashique Jaspers, Stephen Stitt, Trevor Murphy, Andrew J. Yancopoulos, George D. Gromada, Jesper Nat Commun Article 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. Nature Publishing Group 2017-04-28 /pmc/articles/PMC5414365/ /pubmed/28452368 http://dx.doi.org/10.1038/ncomms15153 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Latres, Esther Mastaitis, Jason Fury, Wen Miloscio, Lawrence Trejos, Jesus Pangilinan, Jeffrey Okamoto, Haruka Cavino, Katie Na, Erqian Papatheodorou, Angelos Willer, Tobias Bai, Yu Hae Kim, Jee Rafique, Ashique Jaspers, Stephen Stitt, Trevor Murphy, Andrew J. Yancopoulos, George D. Gromada, Jesper Activin A more prominently regulates muscle mass in primates than does GDF8 |
title | Activin A more prominently regulates muscle mass in primates than does GDF8 |
title_full | Activin A more prominently regulates muscle mass in primates than does GDF8 |
title_fullStr | Activin A more prominently regulates muscle mass in primates than does GDF8 |
title_full_unstemmed | Activin A more prominently regulates muscle mass in primates than does GDF8 |
title_short | Activin A more prominently regulates muscle mass in primates than does GDF8 |
title_sort | activin a more prominently regulates muscle mass in primates than does gdf8 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5414365/ https://www.ncbi.nlm.nih.gov/pubmed/28452368 http://dx.doi.org/10.1038/ncomms15153 |
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