# Mechanism of exercise-derived circulating exosomes as a target for sarcopenia management

**Authors:** Xiangbo Wang, Hui Huang, Jie Chen, Qing Zhang, Zhichao Yuan, Mingyue Yin, Chenggen Peng, Songlin Liu

PMC · DOI: 10.3389/fphys.2025.1680485 · 2026-01-22

## TL;DR

This paper reviews how exercise-derived exosomes may help manage sarcopenia by improving muscle health through various biological mechanisms.

## Contribution

The paper provides a comprehensive review of the biogenesis and systemic roles of exercise-derived exosomes in mitigating sarcopenia.

## Key findings

- Exercise-derived exosomes are produced via ESCRT-dependent and independent pathways and are regulated by RAB and SNARE proteins.
- These exosomes help in muscle repair by reducing lipotoxicity through the FGF21-adiponectin axis and modulating macrophage polarization.
- They also maintain protein homeostasis via miR-29c regulation and offer translational promise as therapeutic targets for sarcopenia.

## Abstract

Sarcopenia, an age-related syndrome characterized by the progressive decline of skeletal muscle mass and function, threatens the health of older adults through underlying mechanisms that include dysregulated protein metabolism, autophagy-mitochondrial dysfunction, chronic inflammation, and impaired regenerative capacity of muscle stem cells. Exercise-derived circulating exosomes, which act as key mediators of intercellular communication, show considerable potential in mitigating sarcopenia-related damage. In this review, we summarize the biogenesis of exercise-induced exosomes, encompassing both ESCRT-dependent and independent pathways, secretion regulated by RAB and SNARE proteins, and their release mediated through mechanical, calcium, metabolic, and neuroendocrine signaling during exercise. We further elaborate on the systemic roles of these exosomes in muscle repair, including alleviating lipotoxicity via the FGF21-adiponectin axis, maintaining protein homeostasis through dual regulation by miR-29c, and ameliorating the inflammatory microenvironment via modulation of macrophage polarization. Finally, we discuss the translational promise of exosomes as therapeutic targets and outline future research directions, offering a conceptual framework for understanding exercise-mediated muscle protection and developing novel interventions.

## Linked entities

- **Proteins:** AGFG1 (ArfGAP with FG repeats 1), SNAR-E (small NF90 (ILF3) associated RNA E)

## Full-text entities

- **Genes:** FGF21 (fibroblast growth factor 21) [NCBI Gene 26291], AGFG1 (ArfGAP with FG repeats 1) [NCBI Gene 3267] {aka HRB, RAB, RIP}, ADIPOQ (adiponectin, C1Q and collagen domain containing) [NCBI Gene 9370] {aka ACDC, ACRP30, ADIPQTL1, ADPN, APM-1, APM1}, SNAR-E (small NF90 (ILF3) associated RNA E) [NCBI Gene 100170220], MIR29C (microRNA 29c) [NCBI Gene 407026] {aka MIRN29C, miRNA29C, mir-29c}
- **Diseases:** inflammation (MESH:D007249), mitochondrial dysfunction (MESH:D028361), Sarcopenia (MESH:D055948)
- **Chemicals:** calcium (MESH:D002118)

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12872562/full.md

---
Source: https://tomesphere.com/paper/PMC12872562