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Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence

The formation of hair follicles, a landmark of mammals, requires complex mesenchymal–epithelial interactions and it is commonly believed that embryonic epidermal cells are the only cells that can respond to hair follicle morphogenetic signals in vivo. Here, we demonstrate that epithelial stem cells...

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Autores principales: Claudinot, Stéphanie, Sakabe, Jun-Ichi, Oshima, Hideo, Gonneau, Christèle, Mitsiadis, Thimios, Littman, Daniel, Bonfanti, Paola, Martens, Geert, Nicolas, Michael, Rochat, Ariane, Barrandon, Yann
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648065/
https://www.ncbi.nlm.nih.gov/pubmed/33159086
http://dx.doi.org/10.1038/s41467-020-19485-3
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author Claudinot, Stéphanie
Sakabe, Jun-Ichi
Oshima, Hideo
Gonneau, Christèle
Mitsiadis, Thimios
Littman, Daniel
Bonfanti, Paola
Martens, Geert
Nicolas, Michael
Rochat, Ariane
Barrandon, Yann
author_facet Claudinot, Stéphanie
Sakabe, Jun-Ichi
Oshima, Hideo
Gonneau, Christèle
Mitsiadis, Thimios
Littman, Daniel
Bonfanti, Paola
Martens, Geert
Nicolas, Michael
Rochat, Ariane
Barrandon, Yann
author_sort Claudinot, Stéphanie
collection PubMed
description The formation of hair follicles, a landmark of mammals, requires complex mesenchymal–epithelial interactions and it is commonly believed that embryonic epidermal cells are the only cells that can respond to hair follicle morphogenetic signals in vivo. Here, we demonstrate that epithelial stem cells of non-skin origin (e.g. that of cornea, oesophagus, vagina, bladder, prostate) that express the transcription factor Tp63, a master gene for the development of epidermis and its appendages, can respond to skin morphogenetic signals. When exposed to a newborn skin microenvironment, these cells express hair-follicle lineage markers and contribute to hair follicles, sebaceous glands and/or epidermis renewal. Our results demonstrate that lineage restriction is not immutable and support the notion that all Tp63-expressing epithelial stem cells, independently of their embryonic origin, have latent skin competence explaining why aberrant hair follicles or sebaceous glands are sometimes observed in non-skin tissues (e.g. in cornea, vagina or thymus).
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spelling pubmed-76480652020-11-10 Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence Claudinot, Stéphanie Sakabe, Jun-Ichi Oshima, Hideo Gonneau, Christèle Mitsiadis, Thimios Littman, Daniel Bonfanti, Paola Martens, Geert Nicolas, Michael Rochat, Ariane Barrandon, Yann Nat Commun Article The formation of hair follicles, a landmark of mammals, requires complex mesenchymal–epithelial interactions and it is commonly believed that embryonic epidermal cells are the only cells that can respond to hair follicle morphogenetic signals in vivo. Here, we demonstrate that epithelial stem cells of non-skin origin (e.g. that of cornea, oesophagus, vagina, bladder, prostate) that express the transcription factor Tp63, a master gene for the development of epidermis and its appendages, can respond to skin morphogenetic signals. When exposed to a newborn skin microenvironment, these cells express hair-follicle lineage markers and contribute to hair follicles, sebaceous glands and/or epidermis renewal. Our results demonstrate that lineage restriction is not immutable and support the notion that all Tp63-expressing epithelial stem cells, independently of their embryonic origin, have latent skin competence explaining why aberrant hair follicles or sebaceous glands are sometimes observed in non-skin tissues (e.g. in cornea, vagina or thymus). Nature Publishing Group UK 2020-11-06 /pmc/articles/PMC7648065/ /pubmed/33159086 http://dx.doi.org/10.1038/s41467-020-19485-3 Text en © The Author(s) 2020 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/.
spellingShingle Article
Claudinot, Stéphanie
Sakabe, Jun-Ichi
Oshima, Hideo
Gonneau, Christèle
Mitsiadis, Thimios
Littman, Daniel
Bonfanti, Paola
Martens, Geert
Nicolas, Michael
Rochat, Ariane
Barrandon, Yann
Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence
title Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence
title_full Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence
title_fullStr Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence
title_full_unstemmed Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence
title_short Tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence
title_sort tp63-expressing adult epithelial stem cells cross lineages boundaries revealing latent hairy skin competence
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7648065/
https://www.ncbi.nlm.nih.gov/pubmed/33159086
http://dx.doi.org/10.1038/s41467-020-19485-3
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