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A stem cell population at the anorectal junction maintains homeostasis and participates in tissue regeneration

At numerous locations of the body, transition zones are localized at the crossroad between two types of epithelium and are frequently associated with neoplasia involving both type of tissues. These transition zones contain cells expressing markers of adult stem cells that can be the target of early...

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Autores principales: Mitoyan, Louciné, Chevrier, Véronique, Hernandez-Vargas, Hector, Ollivier, Alexane, Homayed, Zeinab, Pannequin, Julie, Poizat, Flora, De Biasi-Cador, Cécile, Charafe-Jauffret, Emmanuelle, Ginestier, Christophe, Guasch, Géraldine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115161/
https://www.ncbi.nlm.nih.gov/pubmed/33980830
http://dx.doi.org/10.1038/s41467-021-23034-x
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author Mitoyan, Louciné
Chevrier, Véronique
Hernandez-Vargas, Hector
Ollivier, Alexane
Homayed, Zeinab
Pannequin, Julie
Poizat, Flora
De Biasi-Cador, Cécile
Charafe-Jauffret, Emmanuelle
Ginestier, Christophe
Guasch, Géraldine
author_facet Mitoyan, Louciné
Chevrier, Véronique
Hernandez-Vargas, Hector
Ollivier, Alexane
Homayed, Zeinab
Pannequin, Julie
Poizat, Flora
De Biasi-Cador, Cécile
Charafe-Jauffret, Emmanuelle
Ginestier, Christophe
Guasch, Géraldine
author_sort Mitoyan, Louciné
collection PubMed
description At numerous locations of the body, transition zones are localized at the crossroad between two types of epithelium and are frequently associated with neoplasia involving both type of tissues. These transition zones contain cells expressing markers of adult stem cells that can be the target of early transformation. The mere fact that transition zone cells can merge different architecture with separate functions implies for a unique plasticity that these cells must display in steady state. However, their roles during tissue regeneration in normal and injured state remain unknown. Here, by using in vivo lineage tracing, single-cell transcriptomics, computational modeling and a three-dimensional organoid culture system of transition zone cells, we identify a population of Krt17+ basal cells with multipotent properties at the squamo-columnar anorectal junction that maintain a squamous epithelium during normal homeostasis and can participate in the repair of a glandular epithelium following tissue injury.
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spelling pubmed-81151612021-05-14 A stem cell population at the anorectal junction maintains homeostasis and participates in tissue regeneration Mitoyan, Louciné Chevrier, Véronique Hernandez-Vargas, Hector Ollivier, Alexane Homayed, Zeinab Pannequin, Julie Poizat, Flora De Biasi-Cador, Cécile Charafe-Jauffret, Emmanuelle Ginestier, Christophe Guasch, Géraldine Nat Commun Article At numerous locations of the body, transition zones are localized at the crossroad between two types of epithelium and are frequently associated with neoplasia involving both type of tissues. These transition zones contain cells expressing markers of adult stem cells that can be the target of early transformation. The mere fact that transition zone cells can merge different architecture with separate functions implies for a unique plasticity that these cells must display in steady state. However, their roles during tissue regeneration in normal and injured state remain unknown. Here, by using in vivo lineage tracing, single-cell transcriptomics, computational modeling and a three-dimensional organoid culture system of transition zone cells, we identify a population of Krt17+ basal cells with multipotent properties at the squamo-columnar anorectal junction that maintain a squamous epithelium during normal homeostasis and can participate in the repair of a glandular epithelium following tissue injury. Nature Publishing Group UK 2021-05-12 /pmc/articles/PMC8115161/ /pubmed/33980830 http://dx.doi.org/10.1038/s41467-021-23034-x Text en © The Author(s) 2021, corrected publication 2021 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
Mitoyan, Louciné
Chevrier, Véronique
Hernandez-Vargas, Hector
Ollivier, Alexane
Homayed, Zeinab
Pannequin, Julie
Poizat, Flora
De Biasi-Cador, Cécile
Charafe-Jauffret, Emmanuelle
Ginestier, Christophe
Guasch, Géraldine
A stem cell population at the anorectal junction maintains homeostasis and participates in tissue regeneration
title A stem cell population at the anorectal junction maintains homeostasis and participates in tissue regeneration
title_full A stem cell population at the anorectal junction maintains homeostasis and participates in tissue regeneration
title_fullStr A stem cell population at the anorectal junction maintains homeostasis and participates in tissue regeneration
title_full_unstemmed A stem cell population at the anorectal junction maintains homeostasis and participates in tissue regeneration
title_short A stem cell population at the anorectal junction maintains homeostasis and participates in tissue regeneration
title_sort stem cell population at the anorectal junction maintains homeostasis and participates in tissue regeneration
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8115161/
https://www.ncbi.nlm.nih.gov/pubmed/33980830
http://dx.doi.org/10.1038/s41467-021-23034-x
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