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

J Biosci. 2017 Dec;42(4):575-584. doi: 10.1007/s12038-017-9709-2.

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 30'-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.

MeSH terms

  • Cell Line
  • Cell Movement / drug effects*
  • Cell Proliferation / drug effects*
  • Cyclin-Dependent Kinase 2 / genetics
  • Cyclin-Dependent Kinase 2 / metabolism
  • Cyclin-Dependent Kinase 4 / genetics
  • Cyclin-Dependent Kinase 4 / metabolism
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects*
  • Epithelial Cells / metabolism
  • Epithelial-Mesenchymal Transition / drug effects
  • Fibronectins / genetics
  • Fibronectins / metabolism
  • Gene Expression Regulation
  • Humans
  • Lens, Crystalline / cytology
  • Lens, Crystalline / drug effects
  • Lens, Crystalline / metabolism
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Molecular Mimicry
  • Oligonucleotides / genetics
  • Oligonucleotides / metabolism
  • Phosphorylation
  • Plasmids / chemistry
  • Plasmids / metabolism
  • Signal Transduction
  • Smad2 Protein / agonists
  • Smad2 Protein / genetics*
  • Smad2 Protein / metabolism
  • Transfection
  • Transforming Growth Factor beta2 / antagonists & inhibitors
  • Transforming Growth Factor beta2 / genetics
  • Transforming Growth Factor beta2 / metabolism
  • Transforming Growth Factor beta2 / pharmacology*

Substances

  • Fibronectins
  • MIRN486 microRNA, human
  • MicroRNAs
  • Oligonucleotides
  • SMAD2 protein, human
  • Smad2 Protein
  • TGFB2 protein, human
  • Transforming Growth Factor beta2
  • CDK2 protein, human
  • CDK4 protein, human
  • Cyclin-Dependent Kinase 2
  • Cyclin-Dependent Kinase 4