MicroRNA-486-5p suppresses TGF-β2-induced proliferation, invasion and epithelial–mesenchymal transition of lens epithelial cells by targeting Smad2

B Liu, J Sun, X Lei, Z Zhu, C Pei, L Qin - Journal of biosciences, 2017 - Springer
B Liu, J Sun, X Lei, Z Zhu, C Pei, L Qin
Journal of biosciences, 2017Springer
The pathological development of lens epithelial cells (LECs) leads to posterior capsular
opacification (PCO). This study was undertaken to investigate the effects of microRNA-486-
5p (miR-486-5p) on TGF-β 2-induced proliferation, invasion and epithelial-mesenchymal
transition (EMT) in the lens epithelial cell line SRA01/04, and to explore the underlying
molecular mechanisms. The expression of miR-486-5p in TGF-β 2-induced SRA01/04 cells
was down-regulated, and the expression of Smad2, p-Smad2 and p-Smad3 was up …
Abstract
The pathological development of lens epithelial cells (LECs) leads to posterior capsular opacification (PCO). This study was undertaken to investigate the effects of microRNA-486-5p (miR-486-5p) on TGF-β2-induced proliferation, invasion and epithelial-mesenchymal transition (EMT) in the lens epithelial cell line SRA01/04, and to explore the underlying molecular mechanisms. The expression of miR-486-5p in TGF-β2-induced SRA01/04 cells was down-regulated, and the expression of Smad2, p-Smad2 and p-Smad3 was up-regulated. A dual-luciferase reporter assay revealed that miR-486-5p directly targets the 3′-UTR of Smad2. MiR-486-5p mimic transfection markedly down-regulated the expression levels of Smad2, thus inhibiting the expression of p-Smad2 and p-Smad3. MiR-486-5p overexpression in SRA01/04 cells markedly suppressed TGF-β2-induced proliferation and invasion, inhibited protein expression of CDK2 and CDK4, down-regulated fibronectin, α-SMA and vimentin and up-regulated E-cadherin; these effects were partly reversed by Smad2 overexpression. In short, these data show that miR-486-5p overexpression can inhibit TGF-β2-induced proliferation, invasion and EMT in SRA01/04 cells by repressing Smad2/Smad3 signalling, implying that miR-486-5p may be an effective target to interfere in the progression of PCO.
Springer