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Tissue mechanics drives regeneration of a mucociliated epidermis on the surface of Xenopus embryonic aggregates
Injury, surgery, and disease often disrupt tissues and it is the process of regeneration that aids the restoration of architecture and function. Regeneration can occur through multiple strategies including stem cell expansion, transdifferentiation, or proliferation of differentiated cells. We have i...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994656/ https://www.ncbi.nlm.nih.gov/pubmed/32005801 http://dx.doi.org/10.1038/s41467-020-14385-y |
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author | Kim, Hye Young Jackson, Timothy R. Stuckenholz, Carsten Davidson, Lance A. |
author_facet | Kim, Hye Young Jackson, Timothy R. Stuckenholz, Carsten Davidson, Lance A. |
author_sort | Kim, Hye Young |
collection | PubMed |
description | Injury, surgery, and disease often disrupt tissues and it is the process of regeneration that aids the restoration of architecture and function. Regeneration can occur through multiple strategies including stem cell expansion, transdifferentiation, or proliferation of differentiated cells. We have identified a case of regeneration in Xenopus embryonic aggregates that restores a mucociliated epithelium from mesenchymal cells. Following disruption of embryonic tissue architecture and assembly of a compact mesenchymal aggregate, regeneration first restores an epithelium, transitioning from mesenchymal cells at the surface of the aggregate. Cells establish apico-basal polarity within 5 hours and a mucociliated epithelium within 24 hours. Regeneration coincides with nuclear translocation of the putative mechanotransducer YAP1 and a sharp increase in aggregate stiffness, and regeneration can be controlled by altering stiffness. We propose that regeneration of a mucociliated epithelium occurs in response to biophysical cues sensed by newly exposed cells on the surface of a disrupted mesenchymal tissue. |
format | Online Article Text |
id | pubmed-6994656 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69946562020-02-03 Tissue mechanics drives regeneration of a mucociliated epidermis on the surface of Xenopus embryonic aggregates Kim, Hye Young Jackson, Timothy R. Stuckenholz, Carsten Davidson, Lance A. Nat Commun Article Injury, surgery, and disease often disrupt tissues and it is the process of regeneration that aids the restoration of architecture and function. Regeneration can occur through multiple strategies including stem cell expansion, transdifferentiation, or proliferation of differentiated cells. We have identified a case of regeneration in Xenopus embryonic aggregates that restores a mucociliated epithelium from mesenchymal cells. Following disruption of embryonic tissue architecture and assembly of a compact mesenchymal aggregate, regeneration first restores an epithelium, transitioning from mesenchymal cells at the surface of the aggregate. Cells establish apico-basal polarity within 5 hours and a mucociliated epithelium within 24 hours. Regeneration coincides with nuclear translocation of the putative mechanotransducer YAP1 and a sharp increase in aggregate stiffness, and regeneration can be controlled by altering stiffness. We propose that regeneration of a mucociliated epithelium occurs in response to biophysical cues sensed by newly exposed cells on the surface of a disrupted mesenchymal tissue. Nature Publishing Group UK 2020-01-31 /pmc/articles/PMC6994656/ /pubmed/32005801 http://dx.doi.org/10.1038/s41467-020-14385-y 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 Kim, Hye Young Jackson, Timothy R. Stuckenholz, Carsten Davidson, Lance A. Tissue mechanics drives regeneration of a mucociliated epidermis on the surface of Xenopus embryonic aggregates |
title | Tissue mechanics drives regeneration of a mucociliated epidermis on the surface of Xenopus embryonic aggregates |
title_full | Tissue mechanics drives regeneration of a mucociliated epidermis on the surface of Xenopus embryonic aggregates |
title_fullStr | Tissue mechanics drives regeneration of a mucociliated epidermis on the surface of Xenopus embryonic aggregates |
title_full_unstemmed | Tissue mechanics drives regeneration of a mucociliated epidermis on the surface of Xenopus embryonic aggregates |
title_short | Tissue mechanics drives regeneration of a mucociliated epidermis on the surface of Xenopus embryonic aggregates |
title_sort | tissue mechanics drives regeneration of a mucociliated epidermis on the surface of xenopus embryonic aggregates |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6994656/ https://www.ncbi.nlm.nih.gov/pubmed/32005801 http://dx.doi.org/10.1038/s41467-020-14385-y |
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