CAMVAS

Coordination And Migration of Cells during 3D Vasculogenesis

 Coordinatore FUNDACIO INSTITUT DE BIOENGINYERIA DE CATALUNYA 

 Organization address address: CARRER BALDIRI REIXAC PLANTA 2A 10-12
city: BARCELONA
postcode: 8028

contact info
Titolo: Prof.
Nome: Josep
Cognome: Samitier
Email: send email
Telefono: 34934031145
Fax: 34934039702

 Nazionalità Coordinatore Spain [ES]
 Totale costo 254˙474 €
 EC contributo 254˙474 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2013-IOF
 Funding Scheme MC-IOF
 Anno di inizio 2014
 Periodo (anno-mese-giorno) 2014-10-01   -   2017-09-30

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    FUNDACIO INSTITUT DE BIOENGINYERIA DE CATALUNYA

 Organization address address: CARRER BALDIRI REIXAC PLANTA 2A 10-12
city: BARCELONA
postcode: 8028

contact info
Titolo: Prof.
Nome: Josep
Cognome: Samitier
Email: send email
Telefono: 34934031145
Fax: 34934039702

ES (BARCELONA) coordinator 254˙474.10

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

stem    vasculogenesis    cells    model    guidance    microfluidics    network    chemical    matrix    engineering    coupled    mechanical    host    cancer    cell    tissue   

 Obiettivo del progetto (Objective)

'Cell migration is the core of myriad of phenomena in health and disease. Physical forces exerted during collective cellular motion trigger structural adaptations and signaling events that are of paramount importance in tissue engineering, stem cell differentiation and cancer. A spectacular example of coordinated movements towards a useful endpoint is vasculogenesis, the formation 'de novo' of a network of vessels and capillaries from dispersed endothelial cells. In tissue engineering, precise control of the process of vasculogenesis is essential to create 3D tissue constructs with a proper nutrient and oxygen availability. Such control will only be possible with a deep understanding of cell-cell and cell-matrix mechanical interactions, and biochemical guidance of migrating cells during early 3D vasculogenesis. Providing a theoretical model, experimentally validated, of such multicellular self-organization would highly help in modulating the final architecture of the vascular network. In this project microfluidic experiments are proposed to engineer vasculogenesis within 3D gel matrices, mimicking the native cell environment. The expertise of the outgoing host on microfluidics will ensure the experimental control of chemical and mechanical factors coupled with image acquisition. A continuum-discrete multiscale model, tuned to reproduce mechano-chemical guidance of collectives of cells will be developed in parallel. Measurements of cell-matrix tractions in 3D will be performed at the European host for further mechanical characterization. Traction measurements will be coupled with microfluidics to provide in vitro observations at a high spatiotemporal resolution and extensively validate the in silico model. While advancing the control of 3D vasculogenesis, the project will generate precious knowledge and innovative methodologies that will benefit European research on stem cell mechanobiology during tissue regeneration and in the future, cancer research.'

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