MiR-183 impeded embryo implantation by regulating Hbegf and Lamc1 in mouse uterus

Dingren Cao1, Jingjie Liang1, Fuqiang Feng2

  • 1College of Animal Sciences, Zhejiang University, 866 Yuhangtang Road, Hangzhou 310058, PR China.

Theriogenology
|September 27, 2020
PubMed

Insights

MicroRNA-183 (miR-183) inhibits embryo implantation by suppressing endometrial cell migration and invasion. This finding offers insights into early pregnancy regulation and potential contraceptive development.

Area of Science:

  • Reproductive biology
  • Molecular genetics
  • Developmental biology

Background:

  • Embryo implantation is critical for successful pregnancy.
  • MicroRNAs (miRNAs) are key post-transcriptional regulators, but many roles in implantation remain unclear.
  • microRNA-183 (miR-183) expression varies in the mouse uterus during implantation.

Purpose of the Study:

  • To investigate the function of miR-183 in mouse embryo implantation.
  • To elucidate the molecular mechanisms by which miR-183 affects uterine receptivity.
  • To explore the potential of miR-183 as a target for early pregnancy interventions.

Main Methods:

  • Differential expression analysis of miR-183 in mouse uteri during implantation.
  • In vivo administration of miR-183 agomir to assess effects on implantation sites.
  • Localization studies of miR-183 in the uterine tissue.
  • In vitro gain and loss-of-function experiments in endometrial cell lines.
  • Identification of miR-183 target genes (Hbegf, Lamc1) using molecular binding assays.

Main Results:

  • miR-183 expression is altered in the uterus during embryo implantation.
  • Uterine miR-183 upregulation significantly reduces implantation site numbers.
  • miR-183 inhibits endometrial cell migration, invasion, and apoptosis in vitro.
  • miR-183 directly targets Heparin-Binding EGF-like growth factor (Hbegf) and Laminin gamma one (Lamc1).
  • Maternal factors primarily regulate the observed decrease in miR-183 during implantation.

Conclusions:

  • miR-183 acts as an inhibitor of embryo implantation.
  • The mechanism involves suppressing endometrial cell functions and targeting key implantation genes.
  • miR-183 represents a novel target for developing early pregnancy contraceptives.

Related Concept Videos