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Early satellite cell communication creates a permissive environment for long-term muscle growth

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 c...

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Detalles Bibliográficos
Autores principales: Murach, Kevin A., Peck, Bailey D., Policastro, Robert A., Vechetti, Ivan J., Van Pelt, Douglas W., Dungan, Cory M., Denes, Lance T., Fu, Xu, Brightwell, Camille R., Zentner, Gabriel E., Dupont-Versteegden, Esther E., Richards, Christopher I., Smith, Jeramiah J., Fry, Christopher S., McCarthy, John J., Peterson, Charlotte A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8080523/
https://www.ncbi.nlm.nih.gov/pubmed/33948557
http://dx.doi.org/10.1016/j.isci.2021.102372
Descripción
Sumario: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.