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Low temperature and mTOR inhibition favor stem cell maintenance in human keratinocyte cultures
Adult autologous human epidermal stem cells can be extensively expanded ex vivo for cell and gene therapy. Identifying the mechanisms involved in stem cell maintenance and defining culture conditions to maintain stemness is critical, because an inadequate environment can result in the rapid conversi...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240198/ https://www.ncbi.nlm.nih.gov/pubmed/37139607 http://dx.doi.org/10.15252/embr.202255439 |
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author | Nanba, Daisuke Sakabe, Jun‐Ichi Mosig, Johannes Brouard, Michel Toki, Fujio Shimokawa, Mariko Kamiya, Mako Braschler, Thomas Azzabi, Fahd Droz‐Georget Lathion, Stéphanie Johnsson, Kai Roy, Keya Schmid, Christoph D Bureau, Jean‐Baptiste Rochat, Ariane Barrandon, Yann |
author_facet | Nanba, Daisuke Sakabe, Jun‐Ichi Mosig, Johannes Brouard, Michel Toki, Fujio Shimokawa, Mariko Kamiya, Mako Braschler, Thomas Azzabi, Fahd Droz‐Georget Lathion, Stéphanie Johnsson, Kai Roy, Keya Schmid, Christoph D Bureau, Jean‐Baptiste Rochat, Ariane Barrandon, Yann |
author_sort | Nanba, Daisuke |
collection | PubMed |
description | Adult autologous human epidermal stem cells can be extensively expanded ex vivo for cell and gene therapy. Identifying the mechanisms involved in stem cell maintenance and defining culture conditions to maintain stemness is critical, because an inadequate environment can result in the rapid conversion of stem cells into progenitors/transient amplifying cells (clonal conversion), with deleterious consequences on the quality of the transplants and their ability to engraft. Here, we demonstrate that cultured human epidermal stem cells respond to a small drop in temperature through thermoTRP channels via mTOR signaling. Exposure of cells to rapamycin or a small drop in temperature induces the nuclear translocation of mTOR with an impact on gene expression. We also demonstrate by single‐cell analysis that long‐term inhibition of mTORC1 reduces clonal conversion and favors the maintenance of stemness. Taken together, our results demonstrate that human keratinocyte stem cells can adapt to environmental changes (e.g., small variations in temperature) through mTOR signaling and constant inhibition of mTORC1 favors stem cell maintenance, a finding of high importance for regenerative medicine applications. |
format | Online Article Text |
id | pubmed-10240198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-102401982023-06-06 Low temperature and mTOR inhibition favor stem cell maintenance in human keratinocyte cultures Nanba, Daisuke Sakabe, Jun‐Ichi Mosig, Johannes Brouard, Michel Toki, Fujio Shimokawa, Mariko Kamiya, Mako Braschler, Thomas Azzabi, Fahd Droz‐Georget Lathion, Stéphanie Johnsson, Kai Roy, Keya Schmid, Christoph D Bureau, Jean‐Baptiste Rochat, Ariane Barrandon, Yann EMBO Rep Articles Adult autologous human epidermal stem cells can be extensively expanded ex vivo for cell and gene therapy. Identifying the mechanisms involved in stem cell maintenance and defining culture conditions to maintain stemness is critical, because an inadequate environment can result in the rapid conversion of stem cells into progenitors/transient amplifying cells (clonal conversion), with deleterious consequences on the quality of the transplants and their ability to engraft. Here, we demonstrate that cultured human epidermal stem cells respond to a small drop in temperature through thermoTRP channels via mTOR signaling. Exposure of cells to rapamycin or a small drop in temperature induces the nuclear translocation of mTOR with an impact on gene expression. We also demonstrate by single‐cell analysis that long‐term inhibition of mTORC1 reduces clonal conversion and favors the maintenance of stemness. Taken together, our results demonstrate that human keratinocyte stem cells can adapt to environmental changes (e.g., small variations in temperature) through mTOR signaling and constant inhibition of mTORC1 favors stem cell maintenance, a finding of high importance for regenerative medicine applications. John Wiley and Sons Inc. 2023-05-04 /pmc/articles/PMC10240198/ /pubmed/37139607 http://dx.doi.org/10.15252/embr.202255439 Text en © 2023 The Authors. Published under the terms of the CC BY 4.0 license https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Articles Nanba, Daisuke Sakabe, Jun‐Ichi Mosig, Johannes Brouard, Michel Toki, Fujio Shimokawa, Mariko Kamiya, Mako Braschler, Thomas Azzabi, Fahd Droz‐Georget Lathion, Stéphanie Johnsson, Kai Roy, Keya Schmid, Christoph D Bureau, Jean‐Baptiste Rochat, Ariane Barrandon, Yann Low temperature and mTOR inhibition favor stem cell maintenance in human keratinocyte cultures |
title | Low temperature and mTOR inhibition favor stem cell maintenance in human keratinocyte cultures |
title_full | Low temperature and mTOR inhibition favor stem cell maintenance in human keratinocyte cultures |
title_fullStr | Low temperature and mTOR inhibition favor stem cell maintenance in human keratinocyte cultures |
title_full_unstemmed | Low temperature and mTOR inhibition favor stem cell maintenance in human keratinocyte cultures |
title_short | Low temperature and mTOR inhibition favor stem cell maintenance in human keratinocyte cultures |
title_sort | low temperature and mtor inhibition favor stem cell maintenance in human keratinocyte cultures |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10240198/ https://www.ncbi.nlm.nih.gov/pubmed/37139607 http://dx.doi.org/10.15252/embr.202255439 |
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