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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.

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

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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