Potential role of microRNA-424 in regulating ERRγ to suppress trophoblast proliferation and invasion in fetal growth restriction

Placenta. 2019 Aug:83:57-62. doi: 10.1016/j.placenta.2019.07.001. Epub 2019 Jul 2.

Abstract

Background: Abnormal expression of estrogen-related receptor γ (ERRγ) protein is associated with fetal growth restriction (FGR). The upstream regulators of ERRγ are still unknown.

Objective: To evaluate the placental expression level of microRNA-424 (miR-424) and to demonstrate the relationship between miR-424 and FGR.

Methods: The expression levels of miR-424 were detected in FGR and control placentas. HTR-8/SVneo cells were transfected with mimics or inhibitors to increase or decrease the miR-424 expression level, respectively. The transwell and CCK-8 assays were used to determine trophoblast-derived cell line invasion and proliferation. The expression levels of miR-424, ERRγ, and 17 beta-hydroxysteroid dehydrogenase type 1 (HSD17B1) were detected by qRT-PCR and Western blotting. The relationship between miR-424, ERRγ, and HSD17B1 was determined by luciferase reporter assay.

Results: Compared to the normal pregnancy group, FGR placental tissues showed a significantly higher expression level of miR-424. The up-regulation of miR-424 decreased trophoblast-derived cell line invasion and proliferation. Down-regulation of miR-424 enhanced invasive and proliferative abilities of the cell lines. Over-expression of miR-424 reduced ERRγ protein levels and decreased both mRNA and protein levels of HSD17B1. Thus down-regulation of miR-424 induced protein expression of ERRγ and enhanced the mRNA and protein expressions of HSD17B1. MiR-424 probably mediated the expression of ERRγ via binding to sites other than mRNA 3'UTR.

Conclusion: MiR-424 may be associated with the pathogenesis of FGR by modulating trophoblast-derived cell line proliferation and invasion. MiR-424 may play a role in mediating the protein expressions of ERRγ and HSD17B1.

Keywords: ERRγ; Fetal growth restriction; HSD17B1; Placenta; miR-424.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Cell Line
  • Cell Movement / genetics
  • Cell Movement / physiology
  • Cell Proliferation / genetics
  • Cell Proliferation / physiology
  • Estradiol Dehydrogenases / metabolism
  • Female
  • Fetal Growth Retardation / genetics*
  • Fetal Growth Retardation / metabolism*
  • Fetal Growth Retardation / pathology
  • Humans
  • Infant, Newborn
  • Male
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism*
  • Placenta / metabolism
  • Pregnancy
  • Receptors, Estrogen / genetics
  • Receptors, Estrogen / metabolism*
  • Trophoblasts / metabolism*
  • Trophoblasts / pathology*
  • Young Adult

Substances

  • ESRRG protein, human
  • MIRN424 microrna, human
  • MicroRNAs
  • Receptors, Estrogen
  • Estradiol Dehydrogenases
  • HSD17B1 protein, human