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Cell quiescence in planarian stem cells, interplay between p53 and nutritional stimuli
Cell quiescence appeared early in evolution as an adaptive response to adverse conditions (i.e. nutrient depletion). In metazoans, quiescence has been involved in additional processes like tissue homeostasis, which is made possible by the presence of adult stem cells (ASCs). Cell cycle control machi...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9768645/ https://www.ncbi.nlm.nih.gov/pubmed/36541101 http://dx.doi.org/10.1098/rsob.220216 |
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author | Gambino, Gaetana Iacopetti, Paola Guidi, Patrizia Ippolito, Chiara Linsalata, Stefania Salvetti, Alessandra Rossi, Leonardo |
author_facet | Gambino, Gaetana Iacopetti, Paola Guidi, Patrizia Ippolito, Chiara Linsalata, Stefania Salvetti, Alessandra Rossi, Leonardo |
author_sort | Gambino, Gaetana |
collection | PubMed |
description | Cell quiescence appeared early in evolution as an adaptive response to adverse conditions (i.e. nutrient depletion). In metazoans, quiescence has been involved in additional processes like tissue homeostasis, which is made possible by the presence of adult stem cells (ASCs). Cell cycle control machinery is a common hub for quiescence entrance, and evidence indicates a role for p53 in establishing the quiescent state of undamaged cells. Mechanisms responsible for waking up quiescent cells remain elusive, and nutritional stimulus, as a legacy of its original role, still appears to be a player in quiescence exit. Planarians, rich in ASCs, represent a suitable system in which we characterized a quiescent population of ASCs, the dorsal midline cord (DMC) cells, exhibiting unique transcriptional features and maintained quiescent by p53 and awakened upon feeding. The function of DMC cells is puzzling and we speculate that DMC cells, despite retaining ancient properties, might represent a functional drift in which quiescence has been recruited to provide evolutionary advantages. |
format | Online Article Text |
id | pubmed-9768645 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-97686452022-12-23 Cell quiescence in planarian stem cells, interplay between p53 and nutritional stimuli Gambino, Gaetana Iacopetti, Paola Guidi, Patrizia Ippolito, Chiara Linsalata, Stefania Salvetti, Alessandra Rossi, Leonardo Open Biol Research Cell quiescence appeared early in evolution as an adaptive response to adverse conditions (i.e. nutrient depletion). In metazoans, quiescence has been involved in additional processes like tissue homeostasis, which is made possible by the presence of adult stem cells (ASCs). Cell cycle control machinery is a common hub for quiescence entrance, and evidence indicates a role for p53 in establishing the quiescent state of undamaged cells. Mechanisms responsible for waking up quiescent cells remain elusive, and nutritional stimulus, as a legacy of its original role, still appears to be a player in quiescence exit. Planarians, rich in ASCs, represent a suitable system in which we characterized a quiescent population of ASCs, the dorsal midline cord (DMC) cells, exhibiting unique transcriptional features and maintained quiescent by p53 and awakened upon feeding. The function of DMC cells is puzzling and we speculate that DMC cells, despite retaining ancient properties, might represent a functional drift in which quiescence has been recruited to provide evolutionary advantages. The Royal Society 2022-12-21 /pmc/articles/PMC9768645/ /pubmed/36541101 http://dx.doi.org/10.1098/rsob.220216 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Gambino, Gaetana Iacopetti, Paola Guidi, Patrizia Ippolito, Chiara Linsalata, Stefania Salvetti, Alessandra Rossi, Leonardo Cell quiescence in planarian stem cells, interplay between p53 and nutritional stimuli |
title | Cell quiescence in planarian stem cells, interplay between p53 and nutritional stimuli |
title_full | Cell quiescence in planarian stem cells, interplay between p53 and nutritional stimuli |
title_fullStr | Cell quiescence in planarian stem cells, interplay between p53 and nutritional stimuli |
title_full_unstemmed | Cell quiescence in planarian stem cells, interplay between p53 and nutritional stimuli |
title_short | Cell quiescence in planarian stem cells, interplay between p53 and nutritional stimuli |
title_sort | cell quiescence in planarian stem cells, interplay between p53 and nutritional stimuli |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9768645/ https://www.ncbi.nlm.nih.gov/pubmed/36541101 http://dx.doi.org/10.1098/rsob.220216 |
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