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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2013
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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 |
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author | 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 |
author_facet | 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 |
author_sort | Urciuolo, Anna |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-3682802 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
record_format | MEDLINE/PubMed |
spelling | pubmed-36828022013-12-07 Collagen VI regulates satellite cell self-renewal and muscle regeneration 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 Nat Commun Article 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. 2013 /pmc/articles/PMC3682802/ /pubmed/23743995 http://dx.doi.org/10.1038/ncomms2964 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article 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 Collagen VI regulates satellite cell self-renewal and muscle regeneration |
title | Collagen VI regulates satellite cell self-renewal and muscle regeneration |
title_full | Collagen VI regulates satellite cell self-renewal and muscle regeneration |
title_fullStr | Collagen VI regulates satellite cell self-renewal and muscle regeneration |
title_full_unstemmed | Collagen VI regulates satellite cell self-renewal and muscle regeneration |
title_short | Collagen VI regulates satellite cell self-renewal and muscle regeneration |
title_sort | collagen vi regulates satellite cell self-renewal and muscle regeneration |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3682802/ https://www.ncbi.nlm.nih.gov/pubmed/23743995 http://dx.doi.org/10.1038/ncomms2964 |
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