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Retinoic acid and RARγ maintain satellite cell quiescence through regulation of translation initiation
In adult skeletal muscle, satellite cells are in a quiescent state, which is essential for the future activation of muscle homeostasis and regeneration. Multiple studies have investigated satellite cell proliferation and differentiation, but the molecular mechanisms that safeguard the quiescence of...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9522790/ https://www.ncbi.nlm.nih.gov/pubmed/36175396 http://dx.doi.org/10.1038/s41419-022-05284-9 |
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author | Luo, Wenzhe Xu, Yueyuan Liu, Ruige Liao, Yinlong Wang, Sheng Zhang, Haoyuan Li, Xinyun Wang, Heng |
author_facet | Luo, Wenzhe Xu, Yueyuan Liu, Ruige Liao, Yinlong Wang, Sheng Zhang, Haoyuan Li, Xinyun Wang, Heng |
author_sort | Luo, Wenzhe |
collection | PubMed |
description | In adult skeletal muscle, satellite cells are in a quiescent state, which is essential for the future activation of muscle homeostasis and regeneration. Multiple studies have investigated satellite cell proliferation and differentiation, but the molecular mechanisms that safeguard the quiescence of satellite cells remain largely unknown. In this study, we purposely activated dormant satellite cells by using various stimuli and captured the in vivo-preserved features from quiescence to activation transitions. We found that retinoic acid signaling was required for quiescence maintenance. Mechanistically, retinoic acid receptor gamma (RARγ) binds to and stimulates genes responsible for Akt dephosphorylation and subsequently inhibits overall protein translation initiation in satellite cells. Furthermore, the alleviation of retinoic acid signaling released the satellite cells from quiescence, but this restraint was lost in aged cells. Retinoic acid also preserves the quiescent state during satellite cell isolation, overcoming the cellular stress caused by the isolation process. We conclude that active retinoic acid signaling contributes to the maintenance of the quiescent state of satellite cells through regulation of the protein translation initiation process. |
format | Online Article Text |
id | pubmed-9522790 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-95227902022-10-01 Retinoic acid and RARγ maintain satellite cell quiescence through regulation of translation initiation Luo, Wenzhe Xu, Yueyuan Liu, Ruige Liao, Yinlong Wang, Sheng Zhang, Haoyuan Li, Xinyun Wang, Heng Cell Death Dis Article In adult skeletal muscle, satellite cells are in a quiescent state, which is essential for the future activation of muscle homeostasis and regeneration. Multiple studies have investigated satellite cell proliferation and differentiation, but the molecular mechanisms that safeguard the quiescence of satellite cells remain largely unknown. In this study, we purposely activated dormant satellite cells by using various stimuli and captured the in vivo-preserved features from quiescence to activation transitions. We found that retinoic acid signaling was required for quiescence maintenance. Mechanistically, retinoic acid receptor gamma (RARγ) binds to and stimulates genes responsible for Akt dephosphorylation and subsequently inhibits overall protein translation initiation in satellite cells. Furthermore, the alleviation of retinoic acid signaling released the satellite cells from quiescence, but this restraint was lost in aged cells. Retinoic acid also preserves the quiescent state during satellite cell isolation, overcoming the cellular stress caused by the isolation process. We conclude that active retinoic acid signaling contributes to the maintenance of the quiescent state of satellite cells through regulation of the protein translation initiation process. Nature Publishing Group UK 2022-09-29 /pmc/articles/PMC9522790/ /pubmed/36175396 http://dx.doi.org/10.1038/s41419-022-05284-9 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Luo, Wenzhe Xu, Yueyuan Liu, Ruige Liao, Yinlong Wang, Sheng Zhang, Haoyuan Li, Xinyun Wang, Heng Retinoic acid and RARγ maintain satellite cell quiescence through regulation of translation initiation |
title | Retinoic acid and RARγ maintain satellite cell quiescence through regulation of translation initiation |
title_full | Retinoic acid and RARγ maintain satellite cell quiescence through regulation of translation initiation |
title_fullStr | Retinoic acid and RARγ maintain satellite cell quiescence through regulation of translation initiation |
title_full_unstemmed | Retinoic acid and RARγ maintain satellite cell quiescence through regulation of translation initiation |
title_short | Retinoic acid and RARγ maintain satellite cell quiescence through regulation of translation initiation |
title_sort | retinoic acid and rarγ maintain satellite cell quiescence through regulation of translation initiation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9522790/ https://www.ncbi.nlm.nih.gov/pubmed/36175396 http://dx.doi.org/10.1038/s41419-022-05284-9 |
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