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Epithelial cell plasticity drives endoderm formation during gastrulation

It is generally accepted that epiblast cells ingress into the primitive streak by epithelial-to-mesenchymal transition (EMT) to give rise to the mesoderm; however, it is less clear how the endoderm acquires an epithelial fate. Here, we used embryonic stem cell and mouse embryo knock‐in reporter syst...

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Autores principales: Scheibner, Katharina, Schirge, Silvia, Burtscher, Ingo, Büttner, Maren, Sterr, Michael, Yang, Dapeng, Böttcher, Anika, Ansarullah, Irmler, Martin, Beckers, Johannes, Cernilogar, Filippo M., Schotta, Gunnar, Theis, Fabian J., Lickert, Heiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8277579/
https://www.ncbi.nlm.nih.gov/pubmed/34168324
http://dx.doi.org/10.1038/s41556-021-00694-x
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author Scheibner, Katharina
Schirge, Silvia
Burtscher, Ingo
Büttner, Maren
Sterr, Michael
Yang, Dapeng
Böttcher, Anika
Ansarullah
Irmler, Martin
Beckers, Johannes
Cernilogar, Filippo M.
Schotta, Gunnar
Theis, Fabian J.
Lickert, Heiko
author_facet Scheibner, Katharina
Schirge, Silvia
Burtscher, Ingo
Büttner, Maren
Sterr, Michael
Yang, Dapeng
Böttcher, Anika
Ansarullah
Irmler, Martin
Beckers, Johannes
Cernilogar, Filippo M.
Schotta, Gunnar
Theis, Fabian J.
Lickert, Heiko
author_sort Scheibner, Katharina
collection PubMed
description It is generally accepted that epiblast cells ingress into the primitive streak by epithelial-to-mesenchymal transition (EMT) to give rise to the mesoderm; however, it is less clear how the endoderm acquires an epithelial fate. Here, we used embryonic stem cell and mouse embryo knock‐in reporter systems to combine time-resolved lineage labelling with high-resolution single-cell transcriptomics. This allowed us to resolve the morphogenetic programs that segregate the mesoderm from the endoderm germ layer. Strikingly, while the mesoderm is formed by classical EMT, the endoderm is formed independent of the key EMT transcription factor Snail1 by mechanisms of epithelial cell plasticity. Importantly, forkhead box transcription factor A2 (Foxa2) acts as an epithelial gatekeeper and EMT suppressor to shield the endoderm from undergoing a mesenchymal transition. Altogether, these results not only establish the morphogenetic details of germ layer formation, but also have broader implications for stem cell differentiation and cancer metastasis.
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spelling pubmed-82775792021-08-12 Epithelial cell plasticity drives endoderm formation during gastrulation Scheibner, Katharina Schirge, Silvia Burtscher, Ingo Büttner, Maren Sterr, Michael Yang, Dapeng Böttcher, Anika Ansarullah Irmler, Martin Beckers, Johannes Cernilogar, Filippo M. Schotta, Gunnar Theis, Fabian J. Lickert, Heiko Nat Cell Biol Article It is generally accepted that epiblast cells ingress into the primitive streak by epithelial-to-mesenchymal transition (EMT) to give rise to the mesoderm; however, it is less clear how the endoderm acquires an epithelial fate. Here, we used embryonic stem cell and mouse embryo knock‐in reporter systems to combine time-resolved lineage labelling with high-resolution single-cell transcriptomics. This allowed us to resolve the morphogenetic programs that segregate the mesoderm from the endoderm germ layer. Strikingly, while the mesoderm is formed by classical EMT, the endoderm is formed independent of the key EMT transcription factor Snail1 by mechanisms of epithelial cell plasticity. Importantly, forkhead box transcription factor A2 (Foxa2) acts as an epithelial gatekeeper and EMT suppressor to shield the endoderm from undergoing a mesenchymal transition. Altogether, these results not only establish the morphogenetic details of germ layer formation, but also have broader implications for stem cell differentiation and cancer metastasis. Nature Publishing Group UK 2021-06-24 2021 /pmc/articles/PMC8277579/ /pubmed/34168324 http://dx.doi.org/10.1038/s41556-021-00694-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
Scheibner, Katharina
Schirge, Silvia
Burtscher, Ingo
Büttner, Maren
Sterr, Michael
Yang, Dapeng
Böttcher, Anika
Ansarullah
Irmler, Martin
Beckers, Johannes
Cernilogar, Filippo M.
Schotta, Gunnar
Theis, Fabian J.
Lickert, Heiko
Epithelial cell plasticity drives endoderm formation during gastrulation
title Epithelial cell plasticity drives endoderm formation during gastrulation
title_full Epithelial cell plasticity drives endoderm formation during gastrulation
title_fullStr Epithelial cell plasticity drives endoderm formation during gastrulation
title_full_unstemmed Epithelial cell plasticity drives endoderm formation during gastrulation
title_short Epithelial cell plasticity drives endoderm formation during gastrulation
title_sort epithelial cell plasticity drives endoderm formation during gastrulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8277579/
https://www.ncbi.nlm.nih.gov/pubmed/34168324
http://dx.doi.org/10.1038/s41556-021-00694-x
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