|  Help  |  About  |  Contact Us

Publication : The miR-126 regulates angiopoietin-1 signaling and vessel maturation by targeting p85β.

First Author  Sessa R Year  2012
Journal  Biochim Biophys Acta Volume  1823
Issue  10 Pages  1925-35
PubMed ID  22867989 Mgi Jnum  J:188146
Mgi Id  MGI:5439232 Doi  10.1016/j.bbamcr.2012.07.011
Citation  Sessa R, et al. (2012) The miR-126 regulates Angiopoietin-1 signaling and vessel maturation by targeting p85beta. Biochim Biophys Acta 1823(10):1925-35
abstractText  Blood vessel formation depends on the highly coordinated actions of a variety of angiogenic regulators. Vascular endothelial growth factor (VEGF) and Angiopoietin-1 (Ang-1) are both potent and essential proangiogenic factors with complementary roles in vascular development and function. Whereas VEGF is required for the formation of the initial vascular plexus, Ang-1 contributes to the stabilization and maturation of growing blood vessels. Here, we provide evidence of a novel microRNA (miRNA)-dependent molecular mechanism of Ang-1 signalling modulation aimed at stabilizing adult vasculature. MiRNAs are short non-coding RNA molecules that post-trascriptionally regulate gene expression by translational suppression or in some instances by cleavage of the respective mRNA target. Our data indicate that endothelial cells of mature vessels express high levels of miR-126, which primarily targets phosphoinositide-3-kinase regulatory subunit 2 (p85beta). Down-regulation of miR-126 and over-expression of p85beta in endothelial cells inhibit the biological functions of Ang-1. Additionally, knockdown of miR-126 in zebrafish resulted in vascular remodelling and maturation defects, reminiscent of the Ang-1 loss-of-function phenotype. Our findings suggest that miR-126-mediated phosphoinositide-3-kinase regulation, not only fine-tunes VEGF-signaling, but it strongly enhances the activities of Ang-1 on vessel stabilization and maturation.
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

2 Bio Entities

Trail: Publication

0 Expression