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ISPADMEC

Integrin specificity in rigidity sensitive proliferation, activation and directional migration of endothelial cells

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 ISPADMEC project word cloud

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

morphology    recognize    contractility    selective    biology    ecs    transduce    materials    unmet    precise    matrix    physical    science    tunable    tools    light    extracellular    extracelullar    regulate    endothelial    diversity    topographical    wound    substrate    isolate    ligands    cues    pressing    presentation    answers    vitro    function    scales    encoded    abnormal    regulation    players    regulated    microenvironment    healthy    nanotechnology    nanometer    substrates    viscoelasticity    ec    questions    correlate    unsurprisingly    interdisciplinary    tissue    shed    extraordinary    biochemical    directional    scenarios    activation    cell    intricately    blood    deregulated    strategy    adhesion    summary    length    disease    proliferation    precision    signals    malformation    pathological    structural    fundamental    spreading    migration    healing    functions    minimal    chemical    ecm    cells    contribution    engagement    anticipated    vessel    mechanics    atherosclerosis    protein    mechanical    adhesions    expression    fate    mechanisms    sense    tension    modulate    integrin    micrometer    tumor   

Project "ISPADMEC" data sheet

The following table provides information about the project.

Coordinator
MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV 

Organization address
address: HOFGARTENSTRASSE 8
city: MUENCHEN
postcode: 80539
website: n.a.

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 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  2018-06-26

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV DE (MUENCHEN) coordinator 171˙460.00

Map

 Project objective

Cells have the extraordinary ability to regulate their morphology, functions and fate to minimal changes in the extracelullar microenvironment. Through multi-protein, cell-matrix adhesions they are able to recognize and respond not only to the chemical diversity of the extracellular matrix (ECM), but also to its physical and topographical features. Mechanical and structural cues encoded in the ECM have an essential role in healthy tissue function where contractility, spreading and proliferation are intricately regulated by cell-cell and cell-matrix adhesion and tension. Unsurprisingly, abnormal ECM mechanics are directly associated with disease and tissue malformation (atherosclerosis, wound healing and tumor formation). Understanding the mechanisms cells use to sense and transduce mechanical signals, as well as the contribution of key players in the process is a pressing, unmet challenge. To achieve this goal, I here propose the development of an in vitro strategy that allows precise regulation of both biochemical and mechanical parameters in order to isolate their contribution on fundamental endothelial cell (EC) functions. The proposed work will exploit advances in materials science and nanotechnology to modulate with high precision the presentation of highly selective integrin ligands at the nanometer and micrometer length scales, on substrates with tunable viscoelasticity and mechanics. The anticipated effects of integrin engagement and substrate mechanics on ECs will shed light on how the microenvironment affects their proliferation, activation and directional migration, and help correlate these finding with pathological scenarios where blood vessel mechanics and EC integrin expression are deregulated. In summary, the proposed interdisciplinary approach will contribute both advanced tools to study cells in vitro and crucial answers for specific questions relating to EC biology.

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The information about "ISPADMEC" are provided by the European Opendata Portal: CORDIS opendata.

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