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Rolle der CXCL12 Rezeptoren CXCR4 und CXCR7 in der Atherosklerose und vaskulären Zellhomöostase

Subject Area Cardiology, Angiology
Term from 2007 to 2015
Project identifier Deutsche Forschungsgemeinschaft (DFG) - Project number 29385330
 
Final Report Year 2015

Final Report Abstract

This project has yielded several landmark findings. First of all, the general importance of CXCR4 in protecting against atherosclerosis was demonstrated in a mouse model and this could be related to controlling the homeostasis of neutrophil numbers and function. Next, the differential and cell-specific contributions of CXCR4 on vascular progenitor cells to arterial regeneration could be revealed. Whereas CXCR4 promotes recovery of resident endothelial cells and recruitment of early angiogenic outgrowth cells after arterial injury to limit neointima formation, CXCL12 can drive recruitment of smooth muscle progenitor cells to promote neointima formation as seen in transplant vasculopathy but also the stabilization of primary atherosclerosis. Finally, we have characterized protective effects of the alternative CXCL12 receptor CXCR7 in limiting lesion formation and hyperlipidemia for the first time and have identified a dual complementary pair of endothelial microRNAs for atheroprotection, with miR-126-5p sustaining the proliferative reserve of resident endothelial cells, and miR-126-3p when delivered by apoptotic microparticles inducing auto-regulatory CXCL12 expression to recruit angiogenic cells and thereby promote protective endothelial regeneration. The latter work has been cited about 450-times since 2010, representing a true breakthrough finding.

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