Journal
ISCIENCE
Volume 24, Issue 4, Pages -Publisher
CELL PRESS
DOI: 10.1016/j.isci.2021.102372
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Funding
- NIH National Institutes of Arthritis and Musculoskeletal and Skin Diseases [AR060701, AR071753]
- National Institute on Aging [AG049086, AG063994]
- National Institute of Diabetes and Digestive and Kidney Diseases [DK119619]
- National Institute of General Medical Sciences [GM130349]
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The study demonstrates that satellite cells communicate with other cells in skeletal muscle during mechanical overload, affecting proper long-term extracellular matrix deposition. They modulate chemokine gene expression and influence cell phenotype through extracellular vesicle delivery of miR-206.
Using in vivo muscle stem cell (satellite cell)-specific extracellular vesicle (EV) tracking, satellite cell depletion, in vitro cell culture, and single-cell RNA sequencing, we show satellite cells communicate with other cells in skeletal muscle during mechanical overload. Early satellite cell EV communication primes the muscle milieu for proper long-term extracellular matrix (ECM) deposition and is sufficient to support sustained hypertrophy in adult mice, even in the absence of fusion to muscle fibers. Satellite cells modulate chemokine gene expression across cell types within the first few days of loading, and EV delivery of miR-206 to fibrogenic cells represses Wisp1 expression required for appropriate ECM remodeling. Late-stage communication from myogenic cells during loading is widespread but may be targeted toward endothelial cells. Satellite cells coordinate adaptation by influencing the phenotype of recipient cells, which extends our understanding of their role in muscle adaptation beyond regeneration and myonuclear donation.
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