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TOPOGRAPHYSENSING SIGNED

Effects of 3D topographies on mechanosensing in intestine epithelial architecture and dynamics

Total Cost €

0

EC-Contrib. €

0

Partnership

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 TOPOGRAPHYSENSING project word cloud

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

monolayer    conform    groups    topographic    arrangement    mechanosensing    segregated    beta    locations    interacting    multidisciplinary    microenvironmental    spectrin    organization    laboratory    sophisticated    hypothesis    techniques    mechanisms    curved    disordered    regulation    cellular    tension    molecular    3d    permeates    exposed    generating    integral    defective    precise    organize    ladoux    networks    scrutinize    cadherin    adhesion    versa    sensing    epithelium    cell    2d    sense    biophysics    actin    primarily    spatial    sites    substrates    microfabrication    alpha    form    cues    dynamics    cytoskeletal    vice    context    epcam    topographies    collective    biology    orderly    layered    contractility    epithelial    polarity    interactions    hypothesize    mediated    modulation    mechanotransduction    cytoskeleton    cortical    architecture    tissue    unknown    until    geometric    topographical    cells    forms    modulated    found    network    shows    observations    platform    maintenance    intestine    shown    actomyosin    understand    participates    consists    functions    ankyrin    manner    contrast   

Project "TOPOGRAPHYSENSING" data sheet

The following table provides information about the project.

Coordinator
CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS 

Organization address
address: RUE MICHEL ANGE 3
city: PARIS
postcode: 75794
website: www.cnrs.fr

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 France [FR]
 Total cost 196˙707 €
 EC max contribution 134˙600 € (68%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-09-01   to  2021-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    CENTRE NATIONAL DE LA RECHERCHE SCIENTIFIQUE CNRS FR (PARIS) coordinator 134˙600.00

Map

 Project objective

Intestine epithelium consists of spatially segregated cells that organize into groups of various functions at different locations of the 3D curved epithelial monolayer. How geometric cues contribute to the maintenance of the sophisticated epithelial architecture and dynamics in 3D remains unknown until now. Recently, the Ladoux's laboratory has found that EpCAM-modulated cell contractility associated with the epithelial monolayer polarity, cytoskeletal arrangement, and cell-cell adhesion in 3D context. In contrast to 2D context, the EpCAM-defective tissue shows a loss of collective cellular spatial organization and forms a disordered multi-layered epithelium when exposed to substrates of 3D topographies. In addition, Ankyrin-G and α/β-spectrin network which participates in cortical tension modulation was identified as the main interacting partner with EpCAM in epithelial cells. These observations lead us to hypothesize that EpCAM allows the tissue to sense and conform to complex 3D topographies in an orderly manner. However, the molecular mechanisms and other related functions of EpCAM-mediated mechanotransduction remain unknown. As large scale mechanosensing has been shown to occur primarily through the actin cytoskeleton which permeates the tissue to form a network, we aim to understand the interactions between the EpCAM-mediated pathway and actin modulation and/or E-cadherin adhesion sites that may allow 3D topographical sensing. Our working hypothesis is that EpCAM forms an integral part of the cellular responses to topographic cues that has a more general role in controlling epithelial architecture and dynamics through the regulation of actomyosin networks, or vice versa. Here, we propose to scrutinize EpCAM-mediated mechanotransduction by generating a platform with precise control of geometric factors and microenvironmental cues using a range of multidisciplinary approaches including microfabrication, biophysics, and advanced molecular biology techniques.

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