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Stage-specific effects of Notch activation during skeletal myogenesis
Skeletal myogenesis involves sequential activation, proliferation, self-renewal/differentiation and fusion of myogenic stem cells (satellite cells). Notch signaling is known to be essential for the maintenance of satellite cells, but its function in late-stage myogenesis, i.e. post-differentiation m...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5070950/ https://www.ncbi.nlm.nih.gov/pubmed/27644105 http://dx.doi.org/10.7554/eLife.17355 |
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author | Bi, Pengpeng Yue, Feng Sato, Yusuke Wirbisky, Sara Liu, Weiyi Shan, Tizhong Wen, Yefei Zhou, Daoguo Freeman, Jennifer Kuang, Shihuan |
author_facet | Bi, Pengpeng Yue, Feng Sato, Yusuke Wirbisky, Sara Liu, Weiyi Shan, Tizhong Wen, Yefei Zhou, Daoguo Freeman, Jennifer Kuang, Shihuan |
author_sort | Bi, Pengpeng |
collection | PubMed |
description | Skeletal myogenesis involves sequential activation, proliferation, self-renewal/differentiation and fusion of myogenic stem cells (satellite cells). Notch signaling is known to be essential for the maintenance of satellite cells, but its function in late-stage myogenesis, i.e. post-differentiation myocytes and post-fusion myotubes, is unknown. Using stage-specific Cre alleles, we uncovered distinct roles of Notch1 in mononucleated myocytes and multinucleated myotubes. Specifically, constitutive Notch1 activation dedifferentiates myocytes into Pax7 quiescent satellite cells, leading to severe defects in muscle growth and regeneration, and postnatal lethality. By contrast, myotube-specific Notch1 activation improves the regeneration and exercise performance of aged and dystrophic muscles. Mechanistically, Notch1 activation in myotubes upregulates the expression of Notch ligands, which modulate Notch signaling in the adjacent satellite cells to enhance their regenerative capacity. These results highlight context-dependent effects of Notch activation during myogenesis, and demonstrate that Notch1 activity improves myotube’s function as a stem cell niche. DOI: http://dx.doi.org/10.7554/eLife.17355.001 |
format | Online Article Text |
id | pubmed-5070950 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-50709502016-10-20 Stage-specific effects of Notch activation during skeletal myogenesis Bi, Pengpeng Yue, Feng Sato, Yusuke Wirbisky, Sara Liu, Weiyi Shan, Tizhong Wen, Yefei Zhou, Daoguo Freeman, Jennifer Kuang, Shihuan eLife Developmental Biology and Stem Cells Skeletal myogenesis involves sequential activation, proliferation, self-renewal/differentiation and fusion of myogenic stem cells (satellite cells). Notch signaling is known to be essential for the maintenance of satellite cells, but its function in late-stage myogenesis, i.e. post-differentiation myocytes and post-fusion myotubes, is unknown. Using stage-specific Cre alleles, we uncovered distinct roles of Notch1 in mononucleated myocytes and multinucleated myotubes. Specifically, constitutive Notch1 activation dedifferentiates myocytes into Pax7 quiescent satellite cells, leading to severe defects in muscle growth and regeneration, and postnatal lethality. By contrast, myotube-specific Notch1 activation improves the regeneration and exercise performance of aged and dystrophic muscles. Mechanistically, Notch1 activation in myotubes upregulates the expression of Notch ligands, which modulate Notch signaling in the adjacent satellite cells to enhance their regenerative capacity. These results highlight context-dependent effects of Notch activation during myogenesis, and demonstrate that Notch1 activity improves myotube’s function as a stem cell niche. DOI: http://dx.doi.org/10.7554/eLife.17355.001 eLife Sciences Publications, Ltd 2016-09-19 /pmc/articles/PMC5070950/ /pubmed/27644105 http://dx.doi.org/10.7554/eLife.17355 Text en © 2016, Bi et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Developmental Biology and Stem Cells Bi, Pengpeng Yue, Feng Sato, Yusuke Wirbisky, Sara Liu, Weiyi Shan, Tizhong Wen, Yefei Zhou, Daoguo Freeman, Jennifer Kuang, Shihuan Stage-specific effects of Notch activation during skeletal myogenesis |
title | Stage-specific effects of Notch activation during skeletal myogenesis |
title_full | Stage-specific effects of Notch activation during skeletal myogenesis |
title_fullStr | Stage-specific effects of Notch activation during skeletal myogenesis |
title_full_unstemmed | Stage-specific effects of Notch activation during skeletal myogenesis |
title_short | Stage-specific effects of Notch activation during skeletal myogenesis |
title_sort | stage-specific effects of notch activation during skeletal myogenesis |
topic | Developmental Biology and Stem Cells |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5070950/ https://www.ncbi.nlm.nih.gov/pubmed/27644105 http://dx.doi.org/10.7554/eLife.17355 |
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