| Literature DB >> 26934179 |
Lena Pitzler1,2, Markus Auler1,2, Kristina Probst1,2, Christian Frie1,2, Vera Bergmeier1,2, Tatjana Holzer1,2, Daniele Belluoccio3,4, Jocelyn van den Bergen3,5, Julia Etich1,2, Harald Ehlen1,2, Zhigang Zhou6, Wolfgang Bielke7, Ernst Pöschl6, Mats Paulsson2,8,9, Bent Brachvogel1,2.
Abstract
microRNAs (miRNAs) can regulate the interplay between perivascular cells (PVC) and endothelial cells (EC) during angiogenesis, but the relevant PVC-specific miRNAs are not yet defined. Here, we identified miR-126-3p and miR-146a to be exclusively upregulated in PVC upon interaction with EC, determined their influence on the PVC phenotype and elucidate their molecular mechanisms of action. Specifically the increase of miR-126-3p strongly promoted the motility of PVC on the basement membrane-like composite and stabilized networks of EC. Subsequent miRNA target analysis showed that miR-126-3p inhibits SPRED1 and PLK2 expression, induces ERK1/2 phosphorylation and stimulates TLR3 expression to modulate cell-cell and cell-matrix contacts of PVC. Gain of expression experiments in vivo demonstrated that miR-126-3p stimulates PVC coverage of newly formed vessels and transform immature into mature, less permeable vessels. In conclusion we showed that miR-126-3p regulates matrix-dependent PVC migration and intercellular interaction to modulate vascular integrity. Stem Cells 2016;34:1297-1309.Entities:
Keywords: Angiogenesis; Perivascular cells; Plk2; Spred1; Tlr3; miR-126-3p; miRNA
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Year: 2016 PMID: 26934179 DOI: 10.1002/stem.2308
Source DB: PubMed Journal: Stem Cells ISSN: 1066-5099 Impact factor: 6.277