MiR-9 regulates the post-transcriptional level of VEGF165a by targeting SRPK-1 in ARPE-19 cells

Graefes Arch Clin Exp Ophthalmol. 2014 Sep;252(9):1369-76. doi: 10.1007/s00417-014-2698-z. Epub 2014 Jul 10.

Abstract

Purpose: To investigate the effect of the overexpression of miRNA-9 to the ratio of pro- and anti-angiogenic isoforms of vascular endothelial growth factor (VEGF) in human retinal pigment cells (ARPE-19).

Methods: Oxidative stress was induced to ARPE-19 cells by 4-hydroxynonenal (4-HNE), tert-butyl hydroperoxide (t-BH), and hypoxia chamber with 1% O₂. Expression patterns of miRNAs were validated by qPCR. Relative mRNA levels of VEGF and PEDF were measured by semi-quantitative PCR. After the transfection of miR-9 mimic and inhibitor, transcriptional levels of VEGF165a, VEGF 165b, and SRPK-1 were measured by qPCR.

Results: We demonstrated that miR-9 expression is decreased in ARPE-19 human retinal pigment cells under hypoxic stress induced by 4-HNE, a lipid peroxidation end-product. We observed that miR-9 mimic transfection of ARPE-19 inhibited one of its targets, serine-arginine protein kinase-1 (SRPK-1), modulating the transcriptional level of VEGF165b. Transfection of miR-9 reduced the alternative splicing of VEGF165a mRNA in ARPE-19 cells under hypoxic conditions, suggesting that miR-mediated regulation of alternative splicing could be a potential therapeutic target in neovascular pathologies.

Conclusions: Hypoxic stress decreased the miR-9 level in ARPE-19 cells, which increased the transcriptional level of SRPK-1, resulting in alternative splicing shift to pro-angiogenic isoforms of VEGF165 in human retinal pigment epithelial cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aldehydes / toxicity
  • Cell Line
  • Dose-Response Relationship, Drug
  • Eye Proteins / genetics
  • Gene Expression Regulation / physiology*
  • Humans
  • Immunoblotting
  • MicroRNAs / genetics*
  • Nerve Growth Factors / genetics
  • Oxidative Stress*
  • Protein Serine-Threonine Kinases / genetics*
  • RNA, Messenger / genetics
  • Real-Time Polymerase Chain Reaction
  • Retinal Pigment Epithelium / drug effects
  • Retinal Pigment Epithelium / metabolism*
  • Serpins / genetics
  • Transfection
  • Vascular Endothelial Growth Factor A / genetics*
  • tert-Butylhydroperoxide / toxicity

Substances

  • Aldehydes
  • Eye Proteins
  • MIRN92 microRNA, human
  • MicroRNAs
  • Nerve Growth Factors
  • RNA, Messenger
  • Serpins
  • VEGFA protein, human
  • Vascular Endothelial Growth Factor A
  • pigment epithelium-derived factor
  • tert-Butylhydroperoxide
  • SRPK1 protein, human
  • Protein Serine-Threonine Kinases
  • 4-hydroxy-2-nonenal