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SelforganisingEmbryo SIGNED

Self-organisation across the scales in early mammalian development

Total Cost €

0

EC-Contrib. €

0

Partnership

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 SelforganisingEmbryo project word cloud

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

pressure    cellular    validation    maps    organismal    cell    embryos    understand    capacity    temporally    contact    biology    fate    de    reconstitute    polarisation    paradigm    contractility    sub    extensive    patterns    patterning    position    lack    eggs    blastocyst    single    lineage    domain    suited    sorting    surfaces    lineages    strategies    symmetry    polarity    signalling    coupled    cavities    spaces    outside    cavity    inside    coalescence    broken    expression    fluid    generation    physical    models    expansion    molecular    segregation    mechanisms    cortical    dynamically    subcellular    ultimately    despite    segregates    filled    spatio    relation    embryogenesis    manipulations    integrate    poorly    form    novo    coordinated    live    model    mammals    break    complexities    progressive    unexplored    functional    silico    rest    assembly    gene    signals    organisation    adhesion    dissect    engineer    mouse    free    living    apical    feedback    mechanics    quantification    imaging    reveal    self    generate    physics    scales    specification   

Project "SelforganisingEmbryo" 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]
 Total cost 2˙239˙458 €
 EC max contribution 2˙239˙458 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2016-ADG
 Funding Scheme ERC-ADG
 Starting year 2017
 Duration (year-month-day) from 2017-09-01   to  2022-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    EUROPEAN MOLECULAR BIOLOGY LABORATORY DE (HEIDELBERG) coordinator 2˙239˙458.00

Map

 Project objective

A defining feature of multi-cellular living systems is the capacity to break symmetry and generate patterns through self-organisation. Our project aims to understand the design principle of multi-cellular self-organisation, using a well-suited model system: early mouse embryos. In mammals eggs lack polarity and symmetry is broken during early embryogenesis, which results in segregation of three cell lineages in the blastocyst. Progressive expansion and coalescence of fluid-filled spaces form the blastocyst cavity that segregates the cavity-facing lineage from the rest. Despite extensive gene expression studies, how molecular and physical signals are dynamically coupled for self-organised blastocyst patterning remains poorly understood. We aim to identify the mechanisms of feedback between cell polarity, mechanics (contractility, adhesion, pressure) and fate operating across sub-cellular to whole organismal scales. For this, we adopt a unique set of strategies that integrate biology and physics: advanced live-imaging, quantification of molecular and physical parameters to integrate into lineage maps, reduced systems to establish physical models, and spatio-temporally controlled manipulations for functional validation of those models. We will build up complexities. At the single-cell level, we will study de novo assembly of the apical domain in relation to cell contact and cortical contractility. For inside-outside patterning, we aim to dissect the coordinated signalling between cell position and fate specification. Furthermore, we will study how fluid cavities, a yet unexplored parameter, contribute to cell sorting, apical polarisation and fate specification through generation of pressure and contact-free cell surfaces. Ultimately, we will reconstitute embryogenesis in silico, reveal emerging properties and design engineer the blastocyst. In all, this study will set a paradigm for studying self-organisation on subcellular to organismal scales.

 Publications

year authors and title journal last update
List of publications.
2019 Allyson Quinn Ryan, Chii Jou Chan, François Graner and Takashi Hiiragi
Lumen expansion facilitates epiblast-primitive endoderm fate specification in the mouse blastocyst formation
published pages: , ISSN: , DOI: 10.1101/575282
bioRxiv 2020-04-01
2019 Allyson Quinn Ryan, Chii Jou Chan, François Graner, Takashi Hiiragi
Lumen Expansion Facilitates Epiblast-Primitive Endoderm Fate Specification during Mouse Blastocyst Formation
published pages: 684-697.e4, ISSN: 1534-5807, DOI: 10.1016/j.devcel.2019.10.011
Developmental Cell 51/6 2020-04-01
2019 Chii Jou Chan, Maria Costanzo, Teresa Ruiz-Herrero, Gregor Mönke, Ryan J. Petrie, Martin Bergert, Alba Diz-Muñoz, L. Mahadevan, Takashi Hiiragi
Hydraulic control of mammalian embryo size and cell fate
published pages: 112-116, ISSN: 0028-0836, DOI: 10.1038/s41586-019-1309-x
Nature 571/7763 2020-04-01
2018 Chii Jou Chan, Maria Costanzo, Teresa Ruiz-Herrero, Gregor Mönke, Ryan J. Petrie, L. Mahadevan, Takashi Hiiragi
Hydraulic control of embryo size, tissue shape and cell fate
published pages: , ISSN: , DOI: 10.1101/389619
bioRxiv 2020-04-01
2019 Ritsuya Niwayama, Prachiti Moghe, Yan-Jun Liu, Dimitri Fabrèges, Frank Buchholz, Matthieu Piel, Takashi Hiiragi
A Tug-of-War between Cell Shape and Polarity Controls Division Orientation to Ensure Robust Patterning in the Mouse Blastocyst
published pages: 564-574.e6, ISSN: 1534-5807, DOI: 10.1016/j.devcel.2019.10.012
Developmental Cell 51/5 2020-04-01

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