miR-320 Regulates Glucose-Induced Gene Expression in Diabetes
Author(s) -
Biao Feng,
Subrata Chakrabarti
Publication year - 2012
Publication title -
isrn endocrinology
Language(s) - English
Resource type - Journals
eISSN - 2090-4649
pISSN - 2090-4630
DOI - 10.5402/2012/549875
Subject(s) - umbilical vein , transfection , fibronectin , microrna , vascular endothelial growth factor , microbiology and biotechnology , extracellular matrix , gene expression , chemistry , mapk/erk pathway , downregulation and upregulation , vascular endothelial growth factor a , gene , biology , endocrinology , vegf receptors , cancer research , biochemistry , signal transduction , in vitro
miRNAs play an important role in several biological processes. Here, we investigated miR-320 in glucose-induced augmented production of vasoactive factors and extracellular matrix (ECM) proteins. High glucose exposure decreased the expression of microRNA 320 (miR-320) but increased the expression of endothelin 1 (ET-1), vascular endothelial growth factor (VEGF), and fibronectin (FN) in human umbilical vein endothelial cells (HUVECs). Transfection of miR-320 mimics restored ET-1, VEGF and FN mRNA, and protein expression in HUVECs treated with high glucose. Furthermore, miR-320 mimic transfection reduced glucose-induced augmented production of ERK1/2. Data from this study indicates that miR-320 negatively regulates expression of ET-1, VEGF, and FN through ERK 1/2. Identification of such novel glucose-induced mechanism regulating gene expression may offer a new strategy for the treatment of diabetic complications.
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