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Distinct mesoderm migration phenotypes in extra-embryonic and embryonic regions of the early mouse embryo

In mouse embryo gastrulation, epiblast cells delaminate at the primitive streak to form mesoderm and definitive endoderm, through an epithelial-mesenchymal transition. Mosaic expression of a membrane reporter in nascent mesoderm enabled recording cell shape and trajectory through live imaging. Upon...

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Autores principales: Saykali, Bechara, Mathiah, Navrita, Nahaboo, Wallis, Racu, Marie-Lucie, Hammou, Latifa, Defrance, Matthieu, Migeotte, Isabelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450669/
https://www.ncbi.nlm.nih.gov/pubmed/30950395
http://dx.doi.org/10.7554/eLife.42434
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author Saykali, Bechara
Mathiah, Navrita
Nahaboo, Wallis
Racu, Marie-Lucie
Hammou, Latifa
Defrance, Matthieu
Migeotte, Isabelle
author_facet Saykali, Bechara
Mathiah, Navrita
Nahaboo, Wallis
Racu, Marie-Lucie
Hammou, Latifa
Defrance, Matthieu
Migeotte, Isabelle
author_sort Saykali, Bechara
collection PubMed
description In mouse embryo gastrulation, epiblast cells delaminate at the primitive streak to form mesoderm and definitive endoderm, through an epithelial-mesenchymal transition. Mosaic expression of a membrane reporter in nascent mesoderm enabled recording cell shape and trajectory through live imaging. Upon leaving the streak, cells changed shape and extended protrusions of distinct size and abundance depending on the neighboring germ layer, as well as the region of the embryo. Embryonic trajectories were meandrous but directional, while extra-embryonic mesoderm cells showed little net displacement. Embryonic and extra-embryonic mesoderm transcriptomes highlighted distinct guidance, cytoskeleton, adhesion, and extracellular matrix signatures. Specifically, intermediate filaments were highly expressed in extra-embryonic mesoderm, while live imaging for F-actin showed abundance of actin filaments in embryonic mesoderm only. Accordingly, Rhoa or Rac1 conditional deletion in mesoderm inhibited embryonic, but not extra-embryonic mesoderm migration. Overall, this indicates separate cytoskeleton regulation coordinating the morphology and migration of mesoderm subpopulations.
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spelling pubmed-64506692019-04-08 Distinct mesoderm migration phenotypes in extra-embryonic and embryonic regions of the early mouse embryo Saykali, Bechara Mathiah, Navrita Nahaboo, Wallis Racu, Marie-Lucie Hammou, Latifa Defrance, Matthieu Migeotte, Isabelle eLife Developmental Biology In mouse embryo gastrulation, epiblast cells delaminate at the primitive streak to form mesoderm and definitive endoderm, through an epithelial-mesenchymal transition. Mosaic expression of a membrane reporter in nascent mesoderm enabled recording cell shape and trajectory through live imaging. Upon leaving the streak, cells changed shape and extended protrusions of distinct size and abundance depending on the neighboring germ layer, as well as the region of the embryo. Embryonic trajectories were meandrous but directional, while extra-embryonic mesoderm cells showed little net displacement. Embryonic and extra-embryonic mesoderm transcriptomes highlighted distinct guidance, cytoskeleton, adhesion, and extracellular matrix signatures. Specifically, intermediate filaments were highly expressed in extra-embryonic mesoderm, while live imaging for F-actin showed abundance of actin filaments in embryonic mesoderm only. Accordingly, Rhoa or Rac1 conditional deletion in mesoderm inhibited embryonic, but not extra-embryonic mesoderm migration. Overall, this indicates separate cytoskeleton regulation coordinating the morphology and migration of mesoderm subpopulations. eLife Sciences Publications, Ltd 2019-04-05 /pmc/articles/PMC6450669/ /pubmed/30950395 http://dx.doi.org/10.7554/eLife.42434 Text en © 2019, Saykali et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Saykali, Bechara
Mathiah, Navrita
Nahaboo, Wallis
Racu, Marie-Lucie
Hammou, Latifa
Defrance, Matthieu
Migeotte, Isabelle
Distinct mesoderm migration phenotypes in extra-embryonic and embryonic regions of the early mouse embryo
title Distinct mesoderm migration phenotypes in extra-embryonic and embryonic regions of the early mouse embryo
title_full Distinct mesoderm migration phenotypes in extra-embryonic and embryonic regions of the early mouse embryo
title_fullStr Distinct mesoderm migration phenotypes in extra-embryonic and embryonic regions of the early mouse embryo
title_full_unstemmed Distinct mesoderm migration phenotypes in extra-embryonic and embryonic regions of the early mouse embryo
title_short Distinct mesoderm migration phenotypes in extra-embryonic and embryonic regions of the early mouse embryo
title_sort distinct mesoderm migration phenotypes in extra-embryonic and embryonic regions of the early mouse embryo
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6450669/
https://www.ncbi.nlm.nih.gov/pubmed/30950395
http://dx.doi.org/10.7554/eLife.42434
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