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MecaMorphEME SIGNED

Four-dimensional physical modeling and numerical simulation of the early mouse embryo morphogenesis.

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 MecaMorphEME project word cloud

Explore the words cloud of the MecaMorphEME project. It provides you a very rough idea of what is the project "MecaMorphEME" about.

refined    proteins    transition    unknown    theoretical    progress    accurately    cell    succession    experimental    imaging    divisions    active    cortex    quantitative    mechanism    self    embryo    lineages    internalization    biology    precise    molecular    biophysical    intense    lacks    mouse    model    mammalian    predictions    adhesion    uncover    crosstalk    organize    description    validations    cycles    mechanical    largely    surface    inside    biochemical    cortical    outside    framework    accurate    contractile    dimensional    developmental    theories    physical    actomyosin    regulated    characterization    interdisciplinary    shape    deformations    4d    medicine    primarily    incorporate    segregated    expert    cells    specification    measured    shell    group    close    governing    ultimately    mechanisms    16    layers    regulation    shapes    interface    dynamics    rearrangements    integrating    modeling    designed    reproductive    dynamic    forces    embryos    morphogenesis    principles    reveals   

Project "MecaMorphEME" data sheet

The following table provides information about the project.

Coordinator
EUROPEAN MOLECULAR BIOLOGY LABORATORY 

Organization address
address: Meyerhofstrasse 1
city: HEIDELBERG
postcode: 69117
website: http://www.embl.de

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Germany [DE]
 Project website https://www.virtual-embryo.com/
 Total cost 171˙460 €
 EC max contribution 171˙460 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2014
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2015
 Duration (year-month-day) from 2015-09-01   to  2017-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    EUROPEAN MOLECULAR BIOLOGY LABORATORY DE (HEIDELBERG) coordinator 171˙460.00

Map

 Project objective

The quantitative understanding of the early development of mammalian embryos is essential to the progress of reproductive medicine. Yet, the physical and mechanical principles governing their morphogenesis remain largely unknown. Early mouse embryos self-organize by a succession of cell divisions, deformations and rearrangements, leading ultimately to the specification of two distinct cell lineages, segregated in inside and outside layers. Mechanical forces are therefore as important as biochemical activity in this process and precise 4-dimensional imaging of cells within the embryo reveals intense surface dynamics, regulated by contractile and adhesion proteins. However, our understanding of early embryos development still lacks a precise physical model integrating a dynamic description of the mechanical forces controlling cell shape and cell-cell adhesion.

I will design a 4D physical model of the early mouse embryo providing accurate cell dynamics predictions. Cell shapes are primarily controlled by the actomyosin cortex and they will be described using recently developed cortical active shell theories. To represent accurately cell-cell adhesion dynamics, I will consider the crosstalk between cortical and adhesion proteins activities. Importantly, this model will be designed in close collaboration with an experimental group expert in the biophysical characterization of the mouse embryo, to incorporate measured mechanical parameters and molecular regulation mechanisms. Our model will be refined through cycles of theoretical predictions and experimental validations to uncover the principles of early mammalian embryos development and, more specifically, the mechanism of cell internalization at the 8 to 16 cells transition. This interdisciplinary project, at the interface between physical modeling and developmental biology will provide a unique and accurate biophysical framework for understanding the morphogenesis of early mammalian embryos.

 Publications

year authors and title journal last update
List of publications.
2016 Jean-Léon Maître, Hervé Turlier, Rukshala Illukkumbura, Björn Eismann, Ritsuya Niwayama, François Nédélec, Takashi Hiiragi
Asymmetric division of contractile domains couples cell positioning and fate specification
published pages: 344-348, ISSN: 0028-0836, DOI: 10.1038/nature18958
Nature 536/7616 2019-06-13

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