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Extracellular Vesicles Mediate Communication between Endothelial and Vascular Smooth Muscle Cells
Authors:Marie Fontaine,Sté  phanie Herkenne,Olivier Ek,Alicia Paquot,Amandine Boeckx,Cé  cile Paques,Olivier Nivelles,Marc Thiry,Ingrid Struman
Affiliation:1.Laboratory of Molecular Angiogenesis, GIGA Research Center, University of Liège, B34, 1 Avenue de l’Hôpital, 4000 Liège, Belgium; (M.F.); (S.H.); (O.E.); (A.P.); (A.B.); (C.P.); (O.N.);2.Laboratory of Cell and Tissues Biology, GIGA Research Center, University of Liège, 1 Avenue de l’Hôpital, 4000 Liège, Belgium;
Abstract:The recruitment of pericytes and vascular smooth muscle cells (SMCs) that enwrap endothelial cells (ECs) is a crucial process for vascular maturation and stabilization. Communication between these two cell types is crucial during vascular development and in maintaining vessel homeostasis. Extracellular vesicles (EVs) have emerged as a new communication tool involving the exchange of microRNAs between cells. In the present study, we searched for microRNAs that could be transferred via EVs from ECs to SMCs and vice versa. Thanks to a microRNA profiling experiment, we found that two microRNAs are more exported in each cell type in coculture experiments: while miR-539 is more secreted by ECs, miR-582 is more present in EVs from SMCs. Functional assays revealed that both microRNAs can modulate both cell-type phenotypes. We further identified miR-539 and miR-582 targets, in agreement with their respective cell functions. The results obtained in vivo in the neovascularization model suggest that miR-539 and miR-582 might cooperate to trigger the process of blood vessel coverage by smooth muscle cells in a mature plexus. Taken together, these results are the first to highlight the role of miR-539 and miR-582 in angiogenesis and communication between ECs and SMCs.
Keywords:microRNA   extracellular vesicle   exosome   angiogenesis   miR-539   miR-582
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