MicroRNA-155 inhibits migration of trophoblast cells and contributes to the pathogenesis of severe preeclampsia by regulating endothelial nitric oxide synthase

Mol Med Rep. 2014 Jul;10(1):550-4. doi: 10.3892/mmr.2014.2214. Epub 2014 May 6.

Abstract

The aim of the present study was to characterize the role of microRNA (miR)-155 in the pathogenesis of severe preeclampsia (PE). A total of 19 severe preeclampsic and 22 normal placentas were collected to measure miR-155 and endothelial nitric oxide synthase (eNOS) expression using quantitative (q)PCR and western blot analysis. The results demonstrated a significant increase in the levels of miR-155 and decreased eNOS expression in the severe preeclampsic placentas, as compared with the normal controls. In order to examine the function of miR-155 in the human placenta, the HTR8/Svneo cell line was transiently transfected with an miR-155 mimic or its inhibitor, anti-miR-155. It was confirmed that miR-155 may suppress the expression of eNOS in HTR-8/SVneo cells. Furthermore, a transwell insert invasion assay demonstrated that miR-155 inhibited cell invasion in trophoblast cells, and the effect was rescued by over expression of eNOS. The present study revealed that miR-155 has a negative regulatory role in the migratory behavior of HTR-8/SVneo cells via modulating eNOS.

MeSH terms

  • Adult
  • Cell Line
  • Cell Movement
  • Female
  • Humans
  • MicroRNAs / antagonists & inhibitors
  • MicroRNAs / metabolism*
  • Nitric Oxide Synthase Type III / antagonists & inhibitors
  • Nitric Oxide Synthase Type III / genetics
  • Nitric Oxide Synthase Type III / metabolism*
  • Oligonucleotides, Antisense / metabolism
  • Placenta / enzymology
  • Placenta / metabolism
  • Pre-Eclampsia / enzymology
  • Pre-Eclampsia / genetics
  • Pre-Eclampsia / pathology*
  • Pregnancy
  • RNA Interference
  • RNA, Small Interfering / metabolism
  • Trophoblasts / cytology
  • Up-Regulation

Substances

  • MIRN155 microRNA, human
  • MicroRNAs
  • Oligonucleotides, Antisense
  • RNA, Small Interfering
  • NOS3 protein, human
  • Nitric Oxide Synthase Type III