CALTHERO
Comparative Study And Mechanisms Of Calcification Heterogeneity In Atherosclerotic Plaques
| Coordinatore | UNIVERSITE DE NANTES
Organization address
address: QUAI DE TOURVILLE 1 contact info |
| Nazionalità Coordinatore | France [FR] |
| Totale costo | 194˙046 € |
| EC contributo | 194˙046 € |
| 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-IIF |
| Funding Scheme | MC-IIF |
| Anno di inizio | 2014 |
| Periodo (anno-mese-giorno) | 2014-07-01 - 2016-06-30 |
Partecipanti
| # | ||||
|---|---|---|---|---|
| 1 |
UNIVERSITE DE NANTES
Organization address
address: QUAI DE TOURVILLE 1 contact info |
FR (NANTES CEDEX 1) | coordinator | 194˙046.60 |
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Obiettivo del progetto (Objective)
'Arterial calcifications, like those seen in patients with atherosclerosis, contribute to morbidity and are predictors of premature death. Despite exposure to the same cardiovascular risk factors, previous studies have demonstrated the concept of the heterogeneity of atheroma according to the arterial beds. These differences have a major clinical impact on the occurrence of cardiovascular events (embolism, thrombosis, dissection, restenosis), and recurrence of the disease. The host laboratory recently showed that plaque heterogeneity was notably associated with a difference in calcification burden. Further classification distinguished amorphous from cartilage or even bone structures in the affected vasculature. This process remains poorly understood. This project aims to identify cellular and molecular mechanisms involved in the arterial calcification heterogeneity, by first fully characterizing the lesions in various vascular beds and by associating specific features of the plaque with calcification content. I will also test in vitro the contribution of endothelial cells (EC) and pericytes in vascular cells mineralization and calcification. In particular, I will assess the ability of EC and pericytes to alter macrophage and smooth muscle cell differentiation towards an osteoblast-like cell phenotype. The role of specific molecular pathways (RANK/RANL/OPG...) will be also tested functionally. To further analyze this process in vivo, I will generate double KO mice developing accelerated calcification in lesions and use in vivo fluorescence imaging to monitor plaque formation and calcification over time. Finally, I will assess the predictive clinical impact of the nature of the plaque on intra-stent restenosis in patients following OCT and serial duplex ultrasound imaging. Altogether, this project should greatly contribute to the characterization of the molecular basis of arterial calcification and the difference in bone metabolism in various vascular beds.'