miR‐126‐3p Promotes Matrix‐Dependent Perivascular Cell Attachment, Migration and Intercellular Interaction

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, determin...

Full description

Saved in:
Bibliographic Details
Published inStem cells (Dayton, Ohio) Vol. 34; no. 5; pp. 1297 - 1309
Main Authors Pitzler, Lena, Auler, Markus, Probst, Kristina, Frie, Christian, Bergmeier, Vera, Holzer, Tatjana, Belluoccio, Daniele, van den Bergen, Jocelyn, Etich, Julia, Ehlen, Harald, Zhou, Zhigang, Bielke, Wolfgang, Pöschl, Ernst, Paulsson, Mats, Brachvogel, Bent
Format Journal Article
LanguageEnglish
Published United States Oxford University Press 01.05.2016
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary: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
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:1066-5099
1549-4918
DOI:10.1002/stem.2308