The pregnant mouse uterus exhibits a functional kisspeptin/KISS1R signaling system on the day of embryo implantation

TL;DR

This study shows that the mouse uterus has a functional kisspeptin signaling system on the day of embryo implantation, which may help regulate this process.

Contribution

The study experimentally confirms the functionality of the KP/KISS1R signaling system in the pregnant mouse uterus on D4.

Findings

Kisspeptin triggers p38 and ERK1/2 phosphorylation in the pregnant mouse uterus via KISS1R.

The kisspeptin response is specific to the pregnant uterus on D4 of pregnancy.

The uterus of Kiss1 null mice still expresses functional KISS1R molecules.

Abstract

Expression of kisspeptin (protein) and Kiss1r (mRNA) was recently documented in the mouse uterus on D4 of pregnancy (the day of embryo implantation) suggesting that the uterine-based kisspeptin (KP)/kisspeptin receptor (KISS1R) signaling system regulates embryo implantation. Despite this important suggestion, it was never demonstrated that the uterus actually exhibits a functional KP/KISS1R signaling system on D4 of pregnancy. Thus, the goal of this study was to determine whether a functional KP/KISS1R signaling system exists in the mouse uterus on D4 of pregnancy.

Since kisspeptin/KISS1R signaling triggers the phosphorylation of the mitogen-activated protein kinases p38 and ERK1/2, through immunohistochemical analyses, we determined whether exogenously administered kisspeptin could trigger p38 and ERK1/2 phosphorylation in the uterus on D4 of pregnancy. The results clearly demonstrated that kisspeptin could and that its effects were mediated via KISS1R. Additionally, the robust kisspeptin-triggered response was observed in the pregnant uterus only. Finally, it was demonstrated that on D4 of pregnancy the Kiss1 null uterus expresses functional KISS1R molecules capable of mediating the effects of kisspeptin.

These results lead us to conclude that on D4 of pregnancy, the mouse uterus expresses a functional KP/KISS1R signaling system strengthening the possibility that this signaling system regulates embryo implantation. These findings strengthen the rationale for determining whether such a functional system exists in the uterus of the human female and if so, what role it might play in human pregnancy.

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