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Basal lamina remodeling at the skeletal muscle stem cell niche mediates stem cell self-renewal

A central question in stem cell biology is the relationship between stem cells and their niche. Although previous reports have uncovered how signaling molecules released by niche cells support stem cell function, the role of the extra-cellular matrix (ECM) within the niche is unclear. Here, we show...

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Autores principales: Rayagiri, Shantisree Sandeepani, Ranaldi, Daniele, Raven, Alexander, Mohamad Azhar, Nur Izzah Farhana, Lefebvre, Olivier, Zammit, Peter S, Borycki, Anne-Gaëlle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852002/
https://www.ncbi.nlm.nih.gov/pubmed/29540680
http://dx.doi.org/10.1038/s41467-018-03425-3
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author Rayagiri, Shantisree Sandeepani
Ranaldi, Daniele
Raven, Alexander
Mohamad Azhar, Nur Izzah Farhana
Lefebvre, Olivier
Zammit, Peter S
Borycki, Anne-Gaëlle
author_facet Rayagiri, Shantisree Sandeepani
Ranaldi, Daniele
Raven, Alexander
Mohamad Azhar, Nur Izzah Farhana
Lefebvre, Olivier
Zammit, Peter S
Borycki, Anne-Gaëlle
author_sort Rayagiri, Shantisree Sandeepani
collection PubMed
description A central question in stem cell biology is the relationship between stem cells and their niche. Although previous reports have uncovered how signaling molecules released by niche cells support stem cell function, the role of the extra-cellular matrix (ECM) within the niche is unclear. Here, we show that upon activation, skeletal muscle stem cells (satellite cells) induce local remodeling of the ECM and the deposition of laminin-α1 and laminin-α5 into the basal lamina of the satellite cell niche. Genetic ablation of laminin-α1, disruption of integrin-α6 signaling or blocking matrix metalloproteinase activity impairs satellite cell expansion and self-renewal. Collectively, our findings establish that remodeling of the ECM is an integral process of stem cell activity to support propagation and self-renewal, and may explain the effect laminin-α1-containing supports have on embryonic and adult stem cells, as well as the regenerative activity of exogenous laminin-111 therapy.
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spelling pubmed-58520022018-03-16 Basal lamina remodeling at the skeletal muscle stem cell niche mediates stem cell self-renewal Rayagiri, Shantisree Sandeepani Ranaldi, Daniele Raven, Alexander Mohamad Azhar, Nur Izzah Farhana Lefebvre, Olivier Zammit, Peter S Borycki, Anne-Gaëlle Nat Commun Article A central question in stem cell biology is the relationship between stem cells and their niche. Although previous reports have uncovered how signaling molecules released by niche cells support stem cell function, the role of the extra-cellular matrix (ECM) within the niche is unclear. Here, we show that upon activation, skeletal muscle stem cells (satellite cells) induce local remodeling of the ECM and the deposition of laminin-α1 and laminin-α5 into the basal lamina of the satellite cell niche. Genetic ablation of laminin-α1, disruption of integrin-α6 signaling or blocking matrix metalloproteinase activity impairs satellite cell expansion and self-renewal. Collectively, our findings establish that remodeling of the ECM is an integral process of stem cell activity to support propagation and self-renewal, and may explain the effect laminin-α1-containing supports have on embryonic and adult stem cells, as well as the regenerative activity of exogenous laminin-111 therapy. Nature Publishing Group UK 2018-03-14 /pmc/articles/PMC5852002/ /pubmed/29540680 http://dx.doi.org/10.1038/s41467-018-03425-3 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Rayagiri, Shantisree Sandeepani
Ranaldi, Daniele
Raven, Alexander
Mohamad Azhar, Nur Izzah Farhana
Lefebvre, Olivier
Zammit, Peter S
Borycki, Anne-Gaëlle
Basal lamina remodeling at the skeletal muscle stem cell niche mediates stem cell self-renewal
title Basal lamina remodeling at the skeletal muscle stem cell niche mediates stem cell self-renewal
title_full Basal lamina remodeling at the skeletal muscle stem cell niche mediates stem cell self-renewal
title_fullStr Basal lamina remodeling at the skeletal muscle stem cell niche mediates stem cell self-renewal
title_full_unstemmed Basal lamina remodeling at the skeletal muscle stem cell niche mediates stem cell self-renewal
title_short Basal lamina remodeling at the skeletal muscle stem cell niche mediates stem cell self-renewal
title_sort basal lamina remodeling at the skeletal muscle stem cell niche mediates stem cell self-renewal
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5852002/
https://www.ncbi.nlm.nih.gov/pubmed/29540680
http://dx.doi.org/10.1038/s41467-018-03425-3
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