期刊论文详细信息
Frontiers in Endocrinology
BMSC-Derived Exosomes Inhibit Dexamethasone-Induced Muscle Atrophy via the miR-486-5p/FoxO1 Axis
Shilun Li2  Sijing Liu3  Ting Li4  Chang Liu5  Xiaoxue Bao5  Peng Xue5  Na Wang5  Ziyi Li5  Yukun Li5 
[1] Department of Endocrinology, The Third Hospital of Hebei Medical University, Shijiazhuang, China;Department of Joint Surgery, The Third Hospital of Hebei Medical University, Shijiazhuang, China;Editorial Department of Hebei Medical University, Hebei Medical University, Shijiazhuang, China;Institute of Biomedical Engineering, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China;Key Orthopaedic Biomechanics Laboratory of Hebei Province, Orthopedic Research Institution of Hebei Province, Shijiazhuang, China;
关键词: muscle atrophy;    bone marrow mesenchymal stem cell;    exosomes;    miR-486-5p;    FoxO1;   
DOI  :  10.3389/fendo.2021.681267
来源: DOAJ
【 摘 要 】

Sarcopenia, characterized by reduced muscle function as well as muscle mass, has been a public health problem with increasing prevalence. It might result from aging, injury, hormone imbalance and other catabolic conditions. Recently, exosomes were considered to regulate muscle regeneration and protein synthesis. In order to confirm the effect of BMSC-derived exosomes (BMSC-Exos) on muscle, dexamethasone-induced muscle atrophy was built both in vitro and in vivo. In the present research, BMSC-Exos attenuated the decrease of myotube diameter induced by dexamethasone, indicating that BMSC-Exos played a protective role in skeletal muscle atrophy. Further mechanism analysis exhibited that the content of miR-486-5p in C2C12 myotubes was up-regulated after treated with BMSC-Exos. Meanwhile, BMSC-Exos markedly downregulated the nuclear translocation of FoxO1, which plays an important role in muscle differentiation and atrophy. Importantly, the miR-486-5p inhibitor reversed the decreased expression of FoxO1 induced by BMSC-Exos. In animal experiments, BMSC-Exos inhibited dexamethasone-induced muscle atrophy, and miR-486-5p inhibitor reversed the protective effect of BMSC-Exos. These results indicating that BMSC-derived exosomes inhibit dexamethasone-induced muscle atrophy via miR486-5p/Foxo1 Axis.

【 授权许可】

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