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Inflammation-associated miR-155 activates differentiation of muscular satellite cells
Tissue renewal and muscle regeneration largely rely on the proliferation and differentiation of muscle stem cells called muscular satellite cells (MuSCs). MuSCs are normally quiescent, but they are activated in response to various stimuli, such as inflammation. Activated MuSCs proliferate, migrate,...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6166968/ https://www.ncbi.nlm.nih.gov/pubmed/30273359 http://dx.doi.org/10.1371/journal.pone.0204860 |
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author | Onodera, Yuta Teramura, Takeshi Takehara, Toshiyuki Itokazu, Maki Mori, Tatsufumi Fukuda, Kanji |
author_facet | Onodera, Yuta Teramura, Takeshi Takehara, Toshiyuki Itokazu, Maki Mori, Tatsufumi Fukuda, Kanji |
author_sort | Onodera, Yuta |
collection | PubMed |
description | Tissue renewal and muscle regeneration largely rely on the proliferation and differentiation of muscle stem cells called muscular satellite cells (MuSCs). MuSCs are normally quiescent, but they are activated in response to various stimuli, such as inflammation. Activated MuSCs proliferate, migrate, differentiate, and fuse to form multinucleate myofibers. Meanwhile, inappropriate cues for MuSC activation induce premature differentiation and bring about stem cell loss. Recent studies revealed that stem cell regulation is disrupted in various aged tissues. We found that the expression of microRNA (miR)-155, which is an inflammation-associated miR, is upregulated in MuSCs of aged muscles, and this upregulation activates the differentiation process through suppression of C/ebpβ, which is an important molecule for maintaining MuSC self-renewal. We also found that Notch1 considerably repressed miR-155 expression, and loss of Notch1 induced miR-155 overexpression. Our findings suggest that miR-155 can act as an activator of muscular differentiation and might be responsible for accelerating aging-associated premature differentiation of MuSCs. |
format | Online Article Text |
id | pubmed-6166968 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-61669682018-10-19 Inflammation-associated miR-155 activates differentiation of muscular satellite cells Onodera, Yuta Teramura, Takeshi Takehara, Toshiyuki Itokazu, Maki Mori, Tatsufumi Fukuda, Kanji PLoS One Research Article Tissue renewal and muscle regeneration largely rely on the proliferation and differentiation of muscle stem cells called muscular satellite cells (MuSCs). MuSCs are normally quiescent, but they are activated in response to various stimuli, such as inflammation. Activated MuSCs proliferate, migrate, differentiate, and fuse to form multinucleate myofibers. Meanwhile, inappropriate cues for MuSC activation induce premature differentiation and bring about stem cell loss. Recent studies revealed that stem cell regulation is disrupted in various aged tissues. We found that the expression of microRNA (miR)-155, which is an inflammation-associated miR, is upregulated in MuSCs of aged muscles, and this upregulation activates the differentiation process through suppression of C/ebpβ, which is an important molecule for maintaining MuSC self-renewal. We also found that Notch1 considerably repressed miR-155 expression, and loss of Notch1 induced miR-155 overexpression. Our findings suggest that miR-155 can act as an activator of muscular differentiation and might be responsible for accelerating aging-associated premature differentiation of MuSCs. Public Library of Science 2018-10-01 /pmc/articles/PMC6166968/ /pubmed/30273359 http://dx.doi.org/10.1371/journal.pone.0204860 Text en © 2018 Onodera et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Onodera, Yuta Teramura, Takeshi Takehara, Toshiyuki Itokazu, Maki Mori, Tatsufumi Fukuda, Kanji Inflammation-associated miR-155 activates differentiation of muscular satellite cells |
title | Inflammation-associated miR-155 activates differentiation of muscular satellite cells |
title_full | Inflammation-associated miR-155 activates differentiation of muscular satellite cells |
title_fullStr | Inflammation-associated miR-155 activates differentiation of muscular satellite cells |
title_full_unstemmed | Inflammation-associated miR-155 activates differentiation of muscular satellite cells |
title_short | Inflammation-associated miR-155 activates differentiation of muscular satellite cells |
title_sort | inflammation-associated mir-155 activates differentiation of muscular satellite cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6166968/ https://www.ncbi.nlm.nih.gov/pubmed/30273359 http://dx.doi.org/10.1371/journal.pone.0204860 |
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