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Collagen VI regulates satellite cell self-renewal and muscle regeneration

Adult muscle stem cells, or satellite cells play essential roles in homeostasis and regeneration of skeletal muscles. Satellite cells are located within a niche that includes myofibers and extracellular matrix. The function of specific extracellular matrix molecules in regulating SCs is poorly under...

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Detalles Bibliográficos
Autores principales: Urciuolo, Anna, Quarta, Marco, Morbidoni, Valeria, Gattazzo, Francesca, Molon, Sibilla, Grumati, Paolo, Montemurro, Francesca, Tedesco, Francesco Saverio, Blaauw, Bert, Cossu, Giulio, Vozzi, Giovanni, Rando, Thomas A., Bonaldo, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682802/
https://www.ncbi.nlm.nih.gov/pubmed/23743995
http://dx.doi.org/10.1038/ncomms2964
Descripción
Sumario:Adult muscle stem cells, or satellite cells play essential roles in homeostasis and regeneration of skeletal muscles. Satellite cells are located within a niche that includes myofibers and extracellular matrix. The function of specific extracellular matrix molecules in regulating SCs is poorly understood. Here we show that the extracellular matrix protein collagen VI is a key component of the satellite cell niche. Lack of collagen VI in Col6a1(–/–) mice causes impaired muscle regeneration and reduced satellite cell self-renewal capability after injury. Collagen VI null muscles display significant decrease of stiffness, which is able to compromise the in vitro and in vivo activity of wild-type satellite cells. When collagen VI is reinstated in vivo by grafting wild-type fibroblasts, the biomechanical properties of Col6a1(–/–) muscles are ameliorated and satellite cell defects rescued. Our findings establish a critical role for an extracellular matrix molecule in satellite cell self-renewal and open new venues for therapies of collagen VI-related muscle diseases.