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Mechanical impact of epithelial−mesenchymal transition on epithelial morphogenesis in Drosophila
Epithelial−mesenchymal transition (EMT) is an essential process both in physiological and pathological contexts. Intriguingly, EMT is often associated with tissue invagination during development; however, the impact of EMT on tissue remodeling remain unexplored. Here, we show that at the initiation...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609679/ https://www.ncbi.nlm.nih.gov/pubmed/31273212 http://dx.doi.org/10.1038/s41467-019-10720-0 |
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author | Gracia, Mélanie Theis, Sophie Proag, Amsha Gay, Guillaume Benassayag, Corinne Suzanne, Magali |
author_facet | Gracia, Mélanie Theis, Sophie Proag, Amsha Gay, Guillaume Benassayag, Corinne Suzanne, Magali |
author_sort | Gracia, Mélanie |
collection | PubMed |
description | Epithelial−mesenchymal transition (EMT) is an essential process both in physiological and pathological contexts. Intriguingly, EMT is often associated with tissue invagination during development; however, the impact of EMT on tissue remodeling remain unexplored. Here, we show that at the initiation of the EMT process, cells produce an apico-basal force, orthogonal to the surface of the epithelium, that constitutes an important driving force for tissue invagination in Drosophila. When EMT is ectopically induced, cells starting their delamination generate an orthogonal force and induce ectopic folding. Similarly, during mesoderm invagination, cells undergoing EMT generate an apico-basal force through the formation of apico-basal structures of myosin II. Using both laser microdissection and in silico physical modelling, we show that mesoderm invagination does not proceed if apico-basal forces are impaired, indicating that they constitute driving forces in the folding process. Altogether, these data reveal the mechanical impact of EMT on morphogenesis. |
format | Online Article Text |
id | pubmed-6609679 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66096792019-07-08 Mechanical impact of epithelial−mesenchymal transition on epithelial morphogenesis in Drosophila Gracia, Mélanie Theis, Sophie Proag, Amsha Gay, Guillaume Benassayag, Corinne Suzanne, Magali Nat Commun Article Epithelial−mesenchymal transition (EMT) is an essential process both in physiological and pathological contexts. Intriguingly, EMT is often associated with tissue invagination during development; however, the impact of EMT on tissue remodeling remain unexplored. Here, we show that at the initiation of the EMT process, cells produce an apico-basal force, orthogonal to the surface of the epithelium, that constitutes an important driving force for tissue invagination in Drosophila. When EMT is ectopically induced, cells starting their delamination generate an orthogonal force and induce ectopic folding. Similarly, during mesoderm invagination, cells undergoing EMT generate an apico-basal force through the formation of apico-basal structures of myosin II. Using both laser microdissection and in silico physical modelling, we show that mesoderm invagination does not proceed if apico-basal forces are impaired, indicating that they constitute driving forces in the folding process. Altogether, these data reveal the mechanical impact of EMT on morphogenesis. Nature Publishing Group UK 2019-07-04 /pmc/articles/PMC6609679/ /pubmed/31273212 http://dx.doi.org/10.1038/s41467-019-10720-0 Text en © The Author(s) 2019 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 Gracia, Mélanie Theis, Sophie Proag, Amsha Gay, Guillaume Benassayag, Corinne Suzanne, Magali Mechanical impact of epithelial−mesenchymal transition on epithelial morphogenesis in Drosophila |
title | Mechanical impact of epithelial−mesenchymal transition on epithelial morphogenesis in Drosophila |
title_full | Mechanical impact of epithelial−mesenchymal transition on epithelial morphogenesis in Drosophila |
title_fullStr | Mechanical impact of epithelial−mesenchymal transition on epithelial morphogenesis in Drosophila |
title_full_unstemmed | Mechanical impact of epithelial−mesenchymal transition on epithelial morphogenesis in Drosophila |
title_short | Mechanical impact of epithelial−mesenchymal transition on epithelial morphogenesis in Drosophila |
title_sort | mechanical impact of epithelial−mesenchymal transition on epithelial morphogenesis in drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609679/ https://www.ncbi.nlm.nih.gov/pubmed/31273212 http://dx.doi.org/10.1038/s41467-019-10720-0 |
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