Skeletal Muscle sEVs Mediate Exercise-Induced Cardioprotection in I/R Injury

BACKGROUND: Exercise training has been demonstrated to provide direct endogenous cardioprotection and to reduce cardiovascular disease risk. Skeletal muscle functions not only as an organ for movement but also as a vital secretory organ. However, how muscle-heart crosstalk contributes to exercise-induced cardioprotection remains largely unclear. Here, we investigated the cardioprotective effects of exercise-induced small extracellular vesicles (sEVs) derived from skeletal muscle in myocardial ischemia/reperfusion (MI/R) injury in mice. METHODS: An adeno-associated virus 8-dMCK (double-muscle creatine kinase)-CD63-EGFP (enhanced green fluorescent protein) reporter system was used to track skeletal muscle-derived sEVs in the heart of mice after 4 weeks of exercise. To determine whether sEVs from exercised skeletal muscle mediate cardioprotection, cardiac sEV abundance was increased by intramyocardial injection and decreased by generating skeletal muscle-specific Rab27a knockout mice. The molecular mechanism was elucidated by profiling sEV-enriched microRNAs and validating their functions in cardiomyocytes and mouse MI/R injury models. The translational potential was then assessed in human exercise cohorts. Finally, the therapeutic efficacy was evaluated using miRNA agomirs and adeno-associated virus 8-mediated, skeletal muscle-specific overexpression of miRNAs in MI/R injury models. RESULTS: Exercise promoted the entry of skeletal muscle-derived sEVs into the heart. Skeletal muscle-derived sEVs from exercised mice significantly attenuated MI/R injury by reducing cardiomyocyte apoptosis and improving mitochondrial respiration. Exercise-mediated protection against MI/R injury was attenuated after inhibiting the secretion of sEVs from skeletal muscle. Mechanistically, exercise-enriched sEVs delivered miR-451a and miR-143-3p to cardiomyocytes, thereby modulating the PERK (protein kinase R-like endoplasmic reticulum kinase)-ATF4-CHOP stress-response pathway and the USP46/P53 axis, thus reducing cardiomyocyte death. Skeletal muscle-specific overexpression of miR-451a/143-3p recapitulated the cardioprotective effects of exercise in vivo. Furthermore, exercising humans also showed elevated levels of miR-451a/143-3p in their skeletal muscle and circulating sEVs. CONCLUSIONS: Our study reveals a novel exercise-induced cardioprotective mechanism via muscle-heart crosstalk, highlighting a promising therapeutic approach for treating cardiovascular disease.

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Publication Details

Journal
Circulation Research
Published
2026-11-09
DOI
https://doi.org/10.1161/circresaha.126.328334
Primary Topic
Extracellular vesicles in disease
Type
article
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article

Skeletal Muscle sEVs Mediate Exercise-Induced Cardioprotection in I/R Injury

Thomas Scott Bowen, Junjie Xiao, Yuwei Yan, Marco Mensink et al.
Circulation Research
Extracellular vesicles in disease
article

Skeletal Muscle sEVs Mediate Exercise-Induced Cardioprotection in I/R Injury

Thomas Scott Bowen, Junjie Xiao, Yuwei Yan, Marco Mensink, Xinyi Ren, Dragoş Crețoiu, Dongchao Lu, Meiyu Hu, Harrison Gallagher, Yuying Chen, Guoping Li, Li Qian, Jin Li, Hongjian Chen, Tingting Yang, Qiumeng Nie, Xiaohang Yin, Yanan Zhang, Jingying Chen
article en

Abstract

BACKGROUND: Exercise training has been demonstrated to provide direct endogenous cardioprotection and to reduce cardiovascular disease risk. Skeletal muscle functions not only as an organ for movement but also as a vital secretory organ. However, how muscle-heart crosstalk contributes to exercise-induced cardioprotection remains largely unclear. Here, we investigated the cardioprotective effects of exercise-induced small extracellular vesicles (sEVs) derived from skeletal muscle in myocardial ischemia/reperfusion (MI/R) injury in mice. METHODS: An adeno-associated virus 8-dMCK (double-muscle creatine kinase)-CD63-EGFP (enhanced green fluorescent protein) reporter system was used to track skeletal muscle-derived sEVs in the heart of mice after 4 weeks of exercise. To determine whether sEVs from exercised skeletal muscle mediate cardioprotection, cardiac sEV abundance was increased by intramyocardial injection and decreased by generating skeletal muscle-specific Rab27a knockout mice. The molecular mechanism was elucidated by profiling sEV-enriched microRNAs and validating their functions in cardiomyocytes and mouse MI/R injury models. The translational potential was then assessed in human exercise cohorts. Finally, the therapeutic efficacy was evaluated using miRNA agomirs and adeno-associated virus 8-mediated, skeletal muscle-specific overexpression of miRNAs in MI/R injury models. RESULTS: Exercise promoted the entry of skeletal muscle-derived sEVs into the heart. Skeletal muscle-derived sEVs from exercised mice significantly attenuated MI/R injury by reducing cardiomyocyte apoptosis and improving mitochondrial respiration. Exercise-mediated protection against MI/R injury was attenuated after inhibiting the secretion of sEVs from skeletal muscle. Mechanistically, exercise-enriched sEVs delivered miR-451a and miR-143-3p to cardiomyocytes, thereby modulating the PERK (protein kinase R-like endoplasmic reticulum kinase)-ATF4-CHOP stress-response pathway and the USP46/P53 axis, thus reducing cardiomyocyte death. Skeletal muscle-specific overexpression of miR-451a/143-3p recapitulated the cardioprotective effects of exercise in vivo. Furthermore, exercising humans also showed elevated levels of miR-451a/143-3p in their skeletal muscle and circulating sEVs. CONCLUSIONS: Our study reveals a novel exercise-induced cardioprotective mechanism via muscle-heart crosstalk, highlighting a promising therapeutic approach for treating cardiovascular disease.

Circulation Research
Shanghai University (CN), University of Leeds (GB), Harvard University (US), Carol Davila University of Medicine and Pharmacy (RO), Massachusetts General Hospital (US), Shanghai University of Traditional Chinese Medicine (CN), Institutul National pentru Sanatatea Mamei si Copilului "Alessandrescu-Rusescu" (RO), Wageningen University & Research (NL)
Extracellular vesicles in disease
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