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Thy1 marks a distinct population of slow-cycling stem cells in the mouse epidermis

The presence of distinct stem cells that maintain the interfollicular epidermis is highly debated. Here, we report a population of keratinocytes, marked by Thy1, in the basal layer of the interfollicular epidermis. We find that epidermal cells expressing differential levels of Thy1 display distinct...

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Autores principales: Koren, Elle, Feldman, Alona, Yusupova, Marianna, Kadosh, Avihay, Sedov, Egor, Ankawa, Roi, Yosefzon, Yahav, Nasser, Waseem, Gerstberger, Stefanie, Kimel, Liam B., Priselac, Noa, Brown, Samara, Sharma, Sam, Gorenc, Travis, Shalom-Feuerstein, Ruby, Steller, Hermann, Shemesh, Tom, Fuchs, Yaron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9360001/
https://www.ncbi.nlm.nih.gov/pubmed/35941116
http://dx.doi.org/10.1038/s41467-022-31629-1
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author Koren, Elle
Feldman, Alona
Yusupova, Marianna
Kadosh, Avihay
Sedov, Egor
Ankawa, Roi
Yosefzon, Yahav
Nasser, Waseem
Gerstberger, Stefanie
Kimel, Liam B.
Priselac, Noa
Brown, Samara
Sharma, Sam
Gorenc, Travis
Shalom-Feuerstein, Ruby
Steller, Hermann
Shemesh, Tom
Fuchs, Yaron
author_facet Koren, Elle
Feldman, Alona
Yusupova, Marianna
Kadosh, Avihay
Sedov, Egor
Ankawa, Roi
Yosefzon, Yahav
Nasser, Waseem
Gerstberger, Stefanie
Kimel, Liam B.
Priselac, Noa
Brown, Samara
Sharma, Sam
Gorenc, Travis
Shalom-Feuerstein, Ruby
Steller, Hermann
Shemesh, Tom
Fuchs, Yaron
author_sort Koren, Elle
collection PubMed
description The presence of distinct stem cells that maintain the interfollicular epidermis is highly debated. Here, we report a population of keratinocytes, marked by Thy1, in the basal layer of the interfollicular epidermis. We find that epidermal cells expressing differential levels of Thy1 display distinct transcriptional signatures. Thy1(+) keratinocytes do not express T cell markers, express a unique transcriptional profile, cycle significantly slower than basal epidermal progenitors and display significant expansion potential in vitro. Multicolor lineage tracing analyses and mathematical modeling reveal that Thy1(+) basal keratinocytes do not compete neutrally alike interfollicular progenitors and contribute long-term to both epidermal replenishment and wound repair. Importantly, ablation of Thy1(+) cells strongly impairs these processes, thus indicating the non-redundant function of Thy1(+) stem cells in the epidermis. Collectively, these results reveal a distinct stem cell population that plays a critical role in epidermal homeostasis and repair.
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spelling pubmed-93600012022-08-10 Thy1 marks a distinct population of slow-cycling stem cells in the mouse epidermis Koren, Elle Feldman, Alona Yusupova, Marianna Kadosh, Avihay Sedov, Egor Ankawa, Roi Yosefzon, Yahav Nasser, Waseem Gerstberger, Stefanie Kimel, Liam B. Priselac, Noa Brown, Samara Sharma, Sam Gorenc, Travis Shalom-Feuerstein, Ruby Steller, Hermann Shemesh, Tom Fuchs, Yaron Nat Commun Article The presence of distinct stem cells that maintain the interfollicular epidermis is highly debated. Here, we report a population of keratinocytes, marked by Thy1, in the basal layer of the interfollicular epidermis. We find that epidermal cells expressing differential levels of Thy1 display distinct transcriptional signatures. Thy1(+) keratinocytes do not express T cell markers, express a unique transcriptional profile, cycle significantly slower than basal epidermal progenitors and display significant expansion potential in vitro. Multicolor lineage tracing analyses and mathematical modeling reveal that Thy1(+) basal keratinocytes do not compete neutrally alike interfollicular progenitors and contribute long-term to both epidermal replenishment and wound repair. Importantly, ablation of Thy1(+) cells strongly impairs these processes, thus indicating the non-redundant function of Thy1(+) stem cells in the epidermis. Collectively, these results reveal a distinct stem cell population that plays a critical role in epidermal homeostasis and repair. Nature Publishing Group UK 2022-08-08 /pmc/articles/PMC9360001/ /pubmed/35941116 http://dx.doi.org/10.1038/s41467-022-31629-1 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
Koren, Elle
Feldman, Alona
Yusupova, Marianna
Kadosh, Avihay
Sedov, Egor
Ankawa, Roi
Yosefzon, Yahav
Nasser, Waseem
Gerstberger, Stefanie
Kimel, Liam B.
Priselac, Noa
Brown, Samara
Sharma, Sam
Gorenc, Travis
Shalom-Feuerstein, Ruby
Steller, Hermann
Shemesh, Tom
Fuchs, Yaron
Thy1 marks a distinct population of slow-cycling stem cells in the mouse epidermis
title Thy1 marks a distinct population of slow-cycling stem cells in the mouse epidermis
title_full Thy1 marks a distinct population of slow-cycling stem cells in the mouse epidermis
title_fullStr Thy1 marks a distinct population of slow-cycling stem cells in the mouse epidermis
title_full_unstemmed Thy1 marks a distinct population of slow-cycling stem cells in the mouse epidermis
title_short Thy1 marks a distinct population of slow-cycling stem cells in the mouse epidermis
title_sort thy1 marks a distinct population of slow-cycling stem cells in the mouse epidermis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9360001/
https://www.ncbi.nlm.nih.gov/pubmed/35941116
http://dx.doi.org/10.1038/s41467-022-31629-1
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