MiR-143 and rat embryo implantation

Biochim Biophys Acta. 2015 Apr;1850(4):708-21. doi: 10.1016/j.bbagen.2014.11.023. Epub 2014 Dec 5.

Abstract

Background: To study the role of miR-143 during embryo implantation in rat.

Methods: MiR-143 expression in rat early pregnancy was detected by Northern blot. The relation between miR-143 and Lifr predicted and confirmed by bioinformatics method, dual-luciferase activity assay, Western blot and immunohistochemistry. The role of miR-143 was detected by MTS, Edu and ranswell chamber assays.

Results: The expression level of miR-143 on gestation day 5-8 (g.d. 5-8) was higher than on g.d. 3-4 in uteri of pregnant rat. MiR-143 was mainly localized in the superficial stroma/primary decidual zone, luminal and glandular epithelia. The expression of miR-143 was not significantly influenced by pseudopregnancy, but the activation of delayed implantation and experimentally induced decidualization significantly promoted miR-143 expression. Over-expression of miR-143 in human endometrial stromal cells (ESCs) inhibited cell proliferation, migration and invasion. Knockdown of miR-143 promoted cell proliferation and invasion. The results of recombinant luciferase reporters showed that miR-143 could bind to the 3¢-untranslated region (UTR) of leukemia inhibitory factor receptor (Lifr) to inhibit Lifr translation.

Conclusions: Uterine miR-143 may be involved in the successful pregnancy, especially during the process of blastocyst implantation through regulating Lifr.

General significance: This study may have the potential to provide new insights into the understanding of miR-143 function during embryo implantation.

Keywords: Embryo implantation; Lifr; Rat; Uterus; miR-143.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Movement
  • Cell Proliferation
  • Embryo Implantation*
  • Estradiol / pharmacology
  • Female
  • Humans
  • MicroRNAs / analysis
  • MicroRNAs / physiology*
  • Pregnancy
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, OSM-LIF / genetics
  • Uterus / metabolism

Substances

  • MIRN143 microRNA, rat
  • MicroRNAs
  • Receptors, OSM-LIF
  • Estradiol