miR-29b contributes to multiple types of muscle atrophy
Skeletal muscle atrophy can occur in response to stimuli such as inactivity, fasting, and ageing. Here the authors show that expression of microRNA-29b promotes muscle atrophy by targeting IGF-1 and PI3K, and that its inhibition attenuates atrophy induced by denervation and immobilization in mice.
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2017-05-01
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Series: | Nature Communications |
Online Access: | https://doi.org/10.1038/ncomms15201 |
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doaj-f21c58614d2245499face880f447ae552021-05-11T07:54:05ZengNature Publishing GroupNature Communications2041-17232017-05-018111510.1038/ncomms15201miR-29b contributes to multiple types of muscle atrophyJin Li0Mun Chun Chan1Yan Yu2Yihua Bei3Ping Chen4Qiulian Zhou5Liming Cheng6Lei Chen7Olivia Ziegler8Glenn C. Rowe9Saumya Das10Junjie Xiao11Cardiac Regeneration and Ageing Lab, School of Life Science, Shanghai UniversityCardiovascular Division of the Massachusetts General Hospital and Harvard Medical SchoolDepartment of Spine Surgery, Tongji Hospital, Tongji University School of MedicineCardiac Regeneration and Ageing Lab, School of Life Science, Shanghai UniversityCardiac Regeneration and Ageing Lab, School of Life Science, Shanghai UniversityCardiac Regeneration and Ageing Lab, School of Life Science, Shanghai UniversityDepartment of Spine Surgery, Tongji Hospital, Tongji University School of MedicineDepartment of Spine Surgery, Tongji Hospital, Tongji University School of MedicineCardiovascular Division of the Massachusetts General Hospital and Harvard Medical SchoolDepartment of Medicine, The University of Alabama at BirminghamCardiovascular Division of the Massachusetts General Hospital and Harvard Medical SchoolCardiac Regeneration and Ageing Lab, School of Life Science, Shanghai UniversitySkeletal muscle atrophy can occur in response to stimuli such as inactivity, fasting, and ageing. Here the authors show that expression of microRNA-29b promotes muscle atrophy by targeting IGF-1 and PI3K, and that its inhibition attenuates atrophy induced by denervation and immobilization in mice.https://doi.org/10.1038/ncomms15201 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Jin Li Mun Chun Chan Yan Yu Yihua Bei Ping Chen Qiulian Zhou Liming Cheng Lei Chen Olivia Ziegler Glenn C. Rowe Saumya Das Junjie Xiao |
spellingShingle |
Jin Li Mun Chun Chan Yan Yu Yihua Bei Ping Chen Qiulian Zhou Liming Cheng Lei Chen Olivia Ziegler Glenn C. Rowe Saumya Das Junjie Xiao miR-29b contributes to multiple types of muscle atrophy Nature Communications |
author_facet |
Jin Li Mun Chun Chan Yan Yu Yihua Bei Ping Chen Qiulian Zhou Liming Cheng Lei Chen Olivia Ziegler Glenn C. Rowe Saumya Das Junjie Xiao |
author_sort |
Jin Li |
title |
miR-29b contributes to multiple types of muscle atrophy |
title_short |
miR-29b contributes to multiple types of muscle atrophy |
title_full |
miR-29b contributes to multiple types of muscle atrophy |
title_fullStr |
miR-29b contributes to multiple types of muscle atrophy |
title_full_unstemmed |
miR-29b contributes to multiple types of muscle atrophy |
title_sort |
mir-29b contributes to multiple types of muscle atrophy |
publisher |
Nature Publishing Group |
series |
Nature Communications |
issn |
2041-1723 |
publishDate |
2017-05-01 |
description |
Skeletal muscle atrophy can occur in response to stimuli such as inactivity, fasting, and ageing. Here the authors show that expression of microRNA-29b promotes muscle atrophy by targeting IGF-1 and PI3K, and that its inhibition attenuates atrophy induced by denervation and immobilization in mice. |
url |
https://doi.org/10.1038/ncomms15201 |
work_keys_str_mv |
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1721451465201942528 |