Cargando…

Mechanotransductive cascade of Myo-II-dependent mesoderm and endoderm invaginations in embryo gastrulation

Animal development consists of a cascade of tissue differentiation and shape change. Associated mechanical signals regulate tissue differentiation. Here we demonstrate that endogenous mechanical cues also trigger biochemical pathways, generating the active morphogenetic movements shaping animal deve...

Descripción completa

Detalles Bibliográficos
Autores principales: Mitrossilis, Démosthène, Röper, Jens-Christian, Le Roy, Damien, Driquez, Benjamin, Michel, Aude, Ménager, Christine, Shaw, Gorky, Le Denmat, Simon, Ranno, Laurent, Dumas-Bouchiat, Frédéric, Dempsey, Nora M., Farge, Emmanuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5264015/
https://www.ncbi.nlm.nih.gov/pubmed/28112149
http://dx.doi.org/10.1038/ncomms13883
_version_ 1782500021358297088
author Mitrossilis, Démosthène
Röper, Jens-Christian
Le Roy, Damien
Driquez, Benjamin
Michel, Aude
Ménager, Christine
Shaw, Gorky
Le Denmat, Simon
Ranno, Laurent
Dumas-Bouchiat, Frédéric
Dempsey, Nora M.
Farge, Emmanuel
author_facet Mitrossilis, Démosthène
Röper, Jens-Christian
Le Roy, Damien
Driquez, Benjamin
Michel, Aude
Ménager, Christine
Shaw, Gorky
Le Denmat, Simon
Ranno, Laurent
Dumas-Bouchiat, Frédéric
Dempsey, Nora M.
Farge, Emmanuel
author_sort Mitrossilis, Démosthène
collection PubMed
description Animal development consists of a cascade of tissue differentiation and shape change. Associated mechanical signals regulate tissue differentiation. Here we demonstrate that endogenous mechanical cues also trigger biochemical pathways, generating the active morphogenetic movements shaping animal development through a mechanotransductive cascade of Myo-II medio-apical stabilization. To mimic physiological tissue deformation with a cell scale resolution, liposomes containing magnetic nanoparticles are injected into embryonic epithelia and submitted to time-variable forces generated by a linear array of micrometric soft magnets. Periodic magnetically induced deformations quantitatively phenocopy the soft mechanical endogenous snail-dependent apex pulsations, rescue the medio-apical accumulation of Rok, Myo-II and subsequent mesoderm invagination lacking in sna mutants, in a Fog-dependent mechanotransductive process. Mesoderm invagination then activates Myo-II apical accumulation, in a similar Fog-dependent mechanotransductive process, which in turn initiates endoderm invagination. This reveals the existence of a highly dynamic self-inductive cascade of mesoderm and endoderm invaginations, regulated by mechano-induced medio-apical stabilization of Myo-II.
format Online
Article
Text
id pubmed-5264015
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher Nature Publishing Group
record_format MEDLINE/PubMed
spelling pubmed-52640152017-02-03 Mechanotransductive cascade of Myo-II-dependent mesoderm and endoderm invaginations in embryo gastrulation Mitrossilis, Démosthène Röper, Jens-Christian Le Roy, Damien Driquez, Benjamin Michel, Aude Ménager, Christine Shaw, Gorky Le Denmat, Simon Ranno, Laurent Dumas-Bouchiat, Frédéric Dempsey, Nora M. Farge, Emmanuel Nat Commun Article Animal development consists of a cascade of tissue differentiation and shape change. Associated mechanical signals regulate tissue differentiation. Here we demonstrate that endogenous mechanical cues also trigger biochemical pathways, generating the active morphogenetic movements shaping animal development through a mechanotransductive cascade of Myo-II medio-apical stabilization. To mimic physiological tissue deformation with a cell scale resolution, liposomes containing magnetic nanoparticles are injected into embryonic epithelia and submitted to time-variable forces generated by a linear array of micrometric soft magnets. Periodic magnetically induced deformations quantitatively phenocopy the soft mechanical endogenous snail-dependent apex pulsations, rescue the medio-apical accumulation of Rok, Myo-II and subsequent mesoderm invagination lacking in sna mutants, in a Fog-dependent mechanotransductive process. Mesoderm invagination then activates Myo-II apical accumulation, in a similar Fog-dependent mechanotransductive process, which in turn initiates endoderm invagination. This reveals the existence of a highly dynamic self-inductive cascade of mesoderm and endoderm invaginations, regulated by mechano-induced medio-apical stabilization of Myo-II. Nature Publishing Group 2017-01-23 /pmc/articles/PMC5264015/ /pubmed/28112149 http://dx.doi.org/10.1038/ncomms13883 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Mitrossilis, Démosthène
Röper, Jens-Christian
Le Roy, Damien
Driquez, Benjamin
Michel, Aude
Ménager, Christine
Shaw, Gorky
Le Denmat, Simon
Ranno, Laurent
Dumas-Bouchiat, Frédéric
Dempsey, Nora M.
Farge, Emmanuel
Mechanotransductive cascade of Myo-II-dependent mesoderm and endoderm invaginations in embryo gastrulation
title Mechanotransductive cascade of Myo-II-dependent mesoderm and endoderm invaginations in embryo gastrulation
title_full Mechanotransductive cascade of Myo-II-dependent mesoderm and endoderm invaginations in embryo gastrulation
title_fullStr Mechanotransductive cascade of Myo-II-dependent mesoderm and endoderm invaginations in embryo gastrulation
title_full_unstemmed Mechanotransductive cascade of Myo-II-dependent mesoderm and endoderm invaginations in embryo gastrulation
title_short Mechanotransductive cascade of Myo-II-dependent mesoderm and endoderm invaginations in embryo gastrulation
title_sort mechanotransductive cascade of myo-ii-dependent mesoderm and endoderm invaginations in embryo gastrulation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5264015/
https://www.ncbi.nlm.nih.gov/pubmed/28112149
http://dx.doi.org/10.1038/ncomms13883
work_keys_str_mv AT mitrossilisdemosthene mechanotransductivecascadeofmyoiidependentmesodermandendoderminvaginationsinembryogastrulation
AT roperjenschristian mechanotransductivecascadeofmyoiidependentmesodermandendoderminvaginationsinembryogastrulation
AT leroydamien mechanotransductivecascadeofmyoiidependentmesodermandendoderminvaginationsinembryogastrulation
AT driquezbenjamin mechanotransductivecascadeofmyoiidependentmesodermandendoderminvaginationsinembryogastrulation
AT michelaude mechanotransductivecascadeofmyoiidependentmesodermandendoderminvaginationsinembryogastrulation
AT menagerchristine mechanotransductivecascadeofmyoiidependentmesodermandendoderminvaginationsinembryogastrulation
AT shawgorky mechanotransductivecascadeofmyoiidependentmesodermandendoderminvaginationsinembryogastrulation
AT ledenmatsimon mechanotransductivecascadeofmyoiidependentmesodermandendoderminvaginationsinembryogastrulation
AT rannolaurent mechanotransductivecascadeofmyoiidependentmesodermandendoderminvaginationsinembryogastrulation
AT dumasbouchiatfrederic mechanotransductivecascadeofmyoiidependentmesodermandendoderminvaginationsinembryogastrulation
AT dempseynoram mechanotransductivecascadeofmyoiidependentmesodermandendoderminvaginationsinembryogastrulation
AT fargeemmanuel mechanotransductivecascadeofmyoiidependentmesodermandendoderminvaginationsinembryogastrulation