Expression and function of kisspeptin during mouse decidualization

PLoS One. 2014 May 15;9(5):e97647. doi: 10.1371/journal.pone.0097647. eCollection 2014.

Abstract

Background: Plasma kisspeptin levels dramatically increased during the first trimester of human pregnancy, which is similar to pregnancy specific glycoprotein-human chorionic gonadotropin. However, its particular role in the implantation and decidualization has not been fully unraveled. Here, the study was conducted to investigate the expression and function of kisspeptin in mouse uterus during early pregnancy and decidualization.

Methodology/principal findings: Quantitative PCR results demonstrated that Kiss1 and GPR54 mRNA levels showed dynamic increase in the mouse uterus during early pregnancy and artificially induced decidualization in vivo. KISS-1 and GPR54 proteins were spatiotemporally expressed in decidualizing stromal cells in intact pregnant females, as well as in pseudopregnant mice undergoing artificially induced decidualization. In the ovariectomized mouse uterus, the expression of Kiss1 mRNA was upregulated after progesterone or/and estradiol treatment. Moreover, in a stromal cell culture model, the expression of Kiss1 and GPR54 mRNA gradually rise with the progression of stromal cell decidualization, whereas the attenuated expression of Kiss1 using small interfering RNA approaches significantly blocked the progression of stromal cell decidualization.

Conclusion: our results demonstrated that Kiss1/GPR54 system was involved in promoting uterine decidualization during early pregnancy in mice.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Decidua / metabolism*
  • Embryo Implantation
  • Female
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental*
  • Hormones / chemistry
  • Keratins / metabolism
  • Kisspeptins / metabolism*
  • Mice
  • Pregnancy
  • Pregnancy, Animal
  • RNA, Messenger / metabolism
  • Receptors, G-Protein-Coupled / metabolism
  • Receptors, Kisspeptin-1
  • Steroids / chemistry
  • Uterus / embryology
  • Vimentin / metabolism

Substances

  • Hormones
  • Kiss1 protein, mouse
  • Kiss1r protein, mouse
  • Kisspeptins
  • RNA, Messenger
  • Receptors, G-Protein-Coupled
  • Receptors, Kisspeptin-1
  • Steroids
  • Vimentin
  • Keratins

Grants and funding

This work was supported by the National Natural Science Foundation of China (31260248, 81270668, 30960118 and 30760071) and The 555 project of Jiangxi Province Gan Po Excellence and the Foundation of the Education Department of Jiangxi Province (GJJ12071). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.