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TAK1 modulates satellite stem cell homeostasis and skeletal muscle repair
Satellite cells are resident adult stem cells that are required for regeneration of skeletal muscle. However, signalling mechanisms that regulate satellite cell function are less understood. Here we demonstrate that transforming growth factor-β-activated kinase 1 (TAK1) is important in satellite ste...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682113/ https://www.ncbi.nlm.nih.gov/pubmed/26648529 http://dx.doi.org/10.1038/ncomms10123 |
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author | Ogura, Yuji Hindi, Sajedah M. Sato, Shuichi Xiong, Guangyan Akira, Shizuo Kumar, Ashok |
author_facet | Ogura, Yuji Hindi, Sajedah M. Sato, Shuichi Xiong, Guangyan Akira, Shizuo Kumar, Ashok |
author_sort | Ogura, Yuji |
collection | PubMed |
description | Satellite cells are resident adult stem cells that are required for regeneration of skeletal muscle. However, signalling mechanisms that regulate satellite cell function are less understood. Here we demonstrate that transforming growth factor-β-activated kinase 1 (TAK1) is important in satellite stem cell homeostasis and function. Inactivation of TAK1 in satellite cells inhibits muscle regeneration in adult mice. TAK1 is essential for satellite cell proliferation and its inactivation causes precocious differentiation. Moreover, TAK1-deficient satellite cells exhibit increased oxidative stress and undergo spontaneous cell death, primarily through necroptosis. TAK1 is required for the activation of NF-κB and JNK in satellite cells. Forced activation of NF-κB improves survival and proliferation of TAK1-deficient satellite cells. Furthermore, TAK1-mediated activation of JNK is essential to prevent oxidative stress and precocious differentiation of satellite cells. Collectively, our study suggests that TAK1 is required for maintaining the pool of satellite stem cells and for regenerative myogenesis. |
format | Online Article Text |
id | pubmed-4682113 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-46821132015-12-29 TAK1 modulates satellite stem cell homeostasis and skeletal muscle repair Ogura, Yuji Hindi, Sajedah M. Sato, Shuichi Xiong, Guangyan Akira, Shizuo Kumar, Ashok Nat Commun Article Satellite cells are resident adult stem cells that are required for regeneration of skeletal muscle. However, signalling mechanisms that regulate satellite cell function are less understood. Here we demonstrate that transforming growth factor-β-activated kinase 1 (TAK1) is important in satellite stem cell homeostasis and function. Inactivation of TAK1 in satellite cells inhibits muscle regeneration in adult mice. TAK1 is essential for satellite cell proliferation and its inactivation causes precocious differentiation. Moreover, TAK1-deficient satellite cells exhibit increased oxidative stress and undergo spontaneous cell death, primarily through necroptosis. TAK1 is required for the activation of NF-κB and JNK in satellite cells. Forced activation of NF-κB improves survival and proliferation of TAK1-deficient satellite cells. Furthermore, TAK1-mediated activation of JNK is essential to prevent oxidative stress and precocious differentiation of satellite cells. Collectively, our study suggests that TAK1 is required for maintaining the pool of satellite stem cells and for regenerative myogenesis. Nature Publishing Group 2015-12-09 /pmc/articles/PMC4682113/ /pubmed/26648529 http://dx.doi.org/10.1038/ncomms10123 Text en Copyright © 2015, Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved. http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Ogura, Yuji Hindi, Sajedah M. Sato, Shuichi Xiong, Guangyan Akira, Shizuo Kumar, Ashok TAK1 modulates satellite stem cell homeostasis and skeletal muscle repair |
title | TAK1 modulates satellite stem cell homeostasis and skeletal muscle repair |
title_full | TAK1 modulates satellite stem cell homeostasis and skeletal muscle repair |
title_fullStr | TAK1 modulates satellite stem cell homeostasis and skeletal muscle repair |
title_full_unstemmed | TAK1 modulates satellite stem cell homeostasis and skeletal muscle repair |
title_short | TAK1 modulates satellite stem cell homeostasis and skeletal muscle repair |
title_sort | tak1 modulates satellite stem cell homeostasis and skeletal muscle repair |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4682113/ https://www.ncbi.nlm.nih.gov/pubmed/26648529 http://dx.doi.org/10.1038/ncomms10123 |
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