EOBOTE

Study of Endothelial and Osteoclastic cells cooperation for Bone Tissue Engineering applications

 Coordinatore UNIVERSITE DE BORDEAUX 

 Organization address address: PLACE PEY BERLAND 35
city: BORDEAUX
postcode: 33000

contact info
Titolo: Ms.
Nome: Véronique
Cognome: Debord-Lazaro
Email: send email
Telefono: +33 5 57571557
Fax: +33 5 57571557

 Nazionalità Coordinatore France [FR]
 Totale costo 75˙000 €
 EC contributo 75˙000 €
 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-2011-CIG
 Funding Scheme MC-CIG
 Anno di inizio 2011
 Periodo (anno-mese-giorno) 2011-08-01   -   2014-07-31

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    UNIVERSITE DE BORDEAUX

 Organization address address: PLACE PEY BERLAND 35
city: BORDEAUX
postcode: 33000

contact info
Titolo: Ms.
Nome: Véronique
Cognome: Debord-Lazaro
Email: send email
Telefono: +33 5 57571557
Fax: +33 5 57571557

FR (BORDEAUX) coordinator 0.00
2    UNIVERSITE VICTOR SEGALEN BORDEAUX II

 Organization address address: RUE LEO SAIGNAT 146
city: BORDEAUX CEDEX
postcode: 33076

contact info
Titolo: Ms.
Nome: Véronique
Cognome: Debord-Lazaro
Email: send email
Telefono: +33 5 57571557
Fax: +33 5 57571557

FR (BORDEAUX CEDEX) participant 75˙000.00

Mappa


 Word cloud

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

endothelial    vascularisation    risk    cells    clinical    disorders    osteoclastic    autograft    materials    substitutes    tissue    bone    regeneration    synthetic    osteoporosis    cell    treatment    resorption   

 Obiettivo del progetto (Objective)

'Bone diseases like osteoporosis and osteoarthritis are affecting an increasing number of people worldwide. The short- and long-term consequences are an increasing risk of fractures, total joint replacement and bone grafting. Current treatments of osteoporosis are based on inhibition of bone resorption and at best preserve bone volume but do not improve bone formation together with a high risk of complications like an osteonecrosis of the jaw. Furthermore, in clinical cases of bone loss or during osteoarticular prostheses surgeries, bone autograft remains the ‘gold standard’ for surgeon as bone substitutes or bone filler, respectively. In fact, despite the good clinical results of calcium phosphate materials in the same applications and their advantages over bone autograft, their lack of biological properties is still a major drawback. These examples clearly demonstrate the actual limits of the current clinical solutions in the field of treatment of bone disorders and bone tissue regeneration. A key factor for bone repair is the creation of the vascular network allowing optimal cell colonization and mineralized tissue formation. Recent studies have shown the crucial role of cells responsible of bone resorption (osteoclastic cells) in the initiation bone remodeling but also in the recruitment of blood vessel forming cell (endothelial cells). Taking together, this data can explain major issues caused by bisphosphonates as well as the limited application of synthetic materials for the treatment of bone defect. Thus a better knowledge of the communication between cells would highlight the mechanisms of the vascularisation process. This project aims to characterize the specific interactions between osteoclastic and endothelial cells in order to provide a new route both for the treatment of bone healing disorders and for the functionalization of synthetic bone substitutes. We believe that this strategy will accelerate vascularisation and improve bone tissue regeneration.'

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