Nuclear entry of AS160 as a transcriptional regulator of satellite cells for muscle regeneration

Dysfunction of muscle satellite cells is linked to diabetic myopathy. The mechanisms vitiating muscle satellite cell proliferative activity in diabetes are not well understood. Here, we show that AS160, a key cytosolic Rab-GTPase activating protein (RabGAP) in insulin signaling, is a moonlighting protein regulating muscle satellite cell proliferation as a transcriptional co-factor. Deletion of AS160, but not its GAP-inactive mutation, impairs muscle satellite cell proliferation and consequent muscle regeneration, and exacerbates age-related sarcopenia. Mechanistically, Thr<sup>642</sup> phosphorylation of AS160 promotes its translocation into the nucleus where AS160 functions as a co-factor of Signal Transducer and Activator of Transcription 3 (STAT3). AS160 binds to STAT3 to enhance the transcription of myogenic cascades and consequent muscle satellite cell proliferation. Disruption of the AS160-STAT3 interaction, or inhibition of AS160-Thr<sup>642</sup> phosphorylation, inhibits muscle satellite cell proliferation and impairs muscle regeneration. Together, our findings reveal a moonlighting function of AS160 as a transcriptional co-factor in the nucleus, and have therapeutic implications for muscle regeneration.

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Publication Details

Journal
Nature Communications
Published
2025-10-15
DOI
https://doi.org/10.1038/s41467-025-64220-5
Citations
1
Primary Topic
Muscle Physiology and Disorders
Type
article
Field-Weighted Citation Impact
0.81

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article

Nuclear entry of AS160 as a transcriptional regulator of satellite cells for muscle regeneration

Ye Cao, Tong‐Jin Zhao, Weikuan Feng, Qing Yao et al.
1 citations
Nature Communications
Muscle Physiology and Disorders
0.81
article

Nuclear entry of AS160 as a transcriptional regulator of satellite cells for muscle regeneration

Ye Cao, Tong‐Jin Zhao, Weikuan Feng, Qing Yao, Lei Fang, Yuwei Zhou, Heng Ai, Shuai Chen, Li Zhang, Qiaoli Chen, Xinhua Ye, Hong Yu Wang, Dahai Zhu, Xu Wang, Ping Rong, Xinyu Yang
article en
1 citations

Abstract

Dysfunction of muscle satellite cells is linked to diabetic myopathy. The mechanisms vitiating muscle satellite cell proliferative activity in diabetes are not well understood. Here, we show that AS160, a key cytosolic Rab-GTPase activating protein (RabGAP) in insulin signaling, is a moonlighting protein regulating muscle satellite cell proliferation as a transcriptional co-factor. Deletion of AS160, but not its GAP-inactive mutation, impairs muscle satellite cell proliferation and consequent muscle regeneration, and exacerbates age-related sarcopenia. Mechanistically, Thr<sup>642</sup> phosphorylation of AS160 promotes its translocation into the nucleus where AS160 functions as a co-factor of Signal Transducer and Activator of Transcription 3 (STAT3). AS160 binds to STAT3 to enhance the transcription of myogenic cascades and consequent muscle satellite cell proliferation. Disruption of the AS160-STAT3 interaction, or inhibition of AS160-Thr<sup>642</sup> phosphorylation, inhibits muscle satellite cell proliferation and impairs muscle regeneration. Together, our findings reveal a moonlighting function of AS160 as a transcriptional co-factor in the nucleus, and have therapeutic implications for muscle regeneration.

Nature CommunicationsVol. 16(1)
Anhui Medical University (CN), Chinese Academy of Medical Sciences & Peking Union Medical College (CN), Fudan University (CN), Guangzhou Regenerative Medicine and Health Guangdong Laboratory (CN), Nanjing Drum Tower Hospital (CN), Model Animal Research Center (CN), Changzhou No.2 People's Hospital (CN), Nanjing University (CN)
Nanjing University
Openalex Percentile: Top 23%
Muscle Physiology and Disorders
0.81
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