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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.

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

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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