miRNA-149 targets PARP-2 in endometrial epithelial and stromal cells to regulate the trophoblast attachment process

Mol Hum Reprod. 2021 May 29;27(6):gaab039. doi: 10.1093/molehr/gaab039.

Abstract

Embryo implantation is a highly complex process involving many regulatory factors, including several micro RNAs (miRNAs/miRs). One miRNA present in the stromal cells of normal endometrium is miR-149, which targets poly (ADP-ribose) polymerase 2 (PARP-2), a gene involved in endometrial receptivity for trophoblast implantation. However, the precise role of miR-149 in the endometrial receptivity during blastocyst implantation is still unknown. We studied miR-149-dependent PARP-2 regulation during trophoblast attachment to endometrial epithelial cells. Using FISH, we found that miR-149 is expressed in mouse endometrial epithelial and stromal cells at implantation and inter-implantation sites. Endometrial receptivity for embryo implantation and attachment is inhibited by the upregulation of miR-149 in the endometrium. Our RT-PCR analysis revealed downregulation of miR-149 in the implantation region of the uterus during the receptive stage (Day 5, 0500 h, p.c.) in the mouse. Under in-vitro conditions, miR-149 overexpression in human endometrial epithelial cells (hEECs) abrogated the human trophoblastic cells spheroid and mouse blastocyst attachment. Subsequently, miR-149 also regulates transformed human endometrial stromal cell (T-hESCs) decidualization by downregulating PARP-2 and upregulating caspase-8 proteins. Overexpression of miR-149 in hEECs and downregulated PARP-2 protein expression, reconfirming that PARP-2 is a downstream target of miR-149 in endometrial cells as well. miR-149 is also able to alter the expression of caspase-8, another PARP-2 regulator. In conclusion, our data indicate that miR-149 is one of the regulators of endometrial receptivity and decidualization for trophoblast implantation, and it exerts the effects by acting on the downstream targets PARP-2 and caspase-8.

Keywords: caspase-8; fluorescence in-situ hybridization (FISH); human endometria epithelial cells (hEEC); human trophoblast cells (hTBLC); micro-RNA (miR)-149; poly(ADP-ribose) polymerase-2 (PARP-2); transformed human endometrial epithelial cells (T-hESC); trophoblast attachment; window of endometrial receptivity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3' Untranslated Regions / genetics
  • Animals
  • Apoptosis
  • Base Sequence
  • Binding Sites
  • Biomarkers
  • Caspase 8 / biosynthesis
  • Caspase 8 / genetics
  • Coculture Techniques
  • Computer Simulation
  • Embryo Implantation / physiology*
  • Endometrium / cytology
  • Endometrium / metabolism*
  • Epithelial Cells / metabolism*
  • Female
  • Mice
  • MicroRNAs / genetics*
  • MicroRNAs / metabolism
  • Poly(ADP-ribose) Polymerases / biosynthesis
  • Poly(ADP-ribose) Polymerases / genetics*
  • Pregnancy
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Stromal Cells / metabolism*
  • Trophoblasts / physiology*

Substances

  • 3' Untranslated Regions
  • Biomarkers
  • MIRN149 microRNA, human
  • MIRN149 microRNA, mouse
  • MicroRNAs
  • RNA, Messenger
  • PARP2 protein, human
  • Poly(ADP-ribose) Polymerases
  • Parp2 protein, mouse
  • CASP8 protein, human
  • Casp8 protein, mouse
  • Caspase 8