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Braz. j. med. biol. res ; 48(6): 486-492, 06/2015. tab, graf
Article in English | LILACS | ID: lil-748219

ABSTRACT

The objective of this study was to determine the expression of miR-483 and miR-483* and the relationship among them, their host gene (Igf2), and other cytokines in a murine model of renal fibrosis. The extent of renal fibrosis was visualized using Masson staining, and fibrosis was scored 3 days and 1 and 2 weeks after unilateral ureteral obstruction (UUO). Expression of miR-483, miR-483* and various cytokine mRNAs was detected by real-time polymerase chain reaction (PCR). Expression of miR-483 and miR-483* was significantly upregulated in the UUO model, particularly miR-483 expression was the greatest 2 weeks after surgery. Additionally, miR-483 and miR-483* expression negatively correlated with Bmp7 expression and positively correlated with Igf2, Tgfβ, Hgf, and Ctgf expression, as determined by Pearson's correlation analysis. Hgf expression significantly increased at 1 and 2 weeks after the surgery compared to the control group. This study showed that miR-483 and miR-483* expression was upregulated in a murine UUO model. These data suggest that miR-483 and miR-483* play a role in renal fibrosis and that miR-483* may interact with miR-483 in renal fibrosis. Thus, these miRNAs may play a role in the pathogenesis of renal fibrosis and coexpression of their host gene Igf2.


Subject(s)
Animals , Male , Mice , Gene Expression , Introns , Insulin-Like Growth Factor II/genetics , MicroRNAs , Ureteral Obstruction/genetics , Ureteral Obstruction/pathology , Blotting, Western , Cytokines/genetics , Disease Models, Animal , Fibrosis/genetics , Kidney/pathology , Real-Time Polymerase Chain Reaction , Time Factors
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