School of Human Sciences, The University of Western Australia, Perth, WA 6009, Australia.
School of Medical and Health Sciences, Edith Cowan University, Joondalup, WA 6027, Australia.
Reprod Fertil Dev. 2024 Jul;36. doi: 10.1071/RD23230.
Context There is mounting evidence implicating kisspeptin signalling in placental development and function. Aims This study aimed to elucidate kisspeptin's role in trophoblast invasion and migration using three experimental models. Methods First, we examined the mouse fetus and placenta in a kisspeptin receptor (Kiss1r) knockout (KO) model. Fetal/placental weights and gene expression (quantitative polymerase chain reaction) were assessed. Second, we determined kisspeptin effects on a human trophoblast (BeWo) cell line in vitro . Third, we examined KISS1 and KISS1R gene expression in human placenta from term and pre-term pregnancies. Key results No difference was found in fetal or placental weight between Kiss1r KO and wildtype mice. However, expression of the trophoblast invasion marker, Mmp2 mRNA, was greater in the placental labyrinth zone of Kiss1r KO mice. BeWo cell models of villus cytotrophoblast and syncytiotrophoblast cells exhibited kisspeptin protein expression, with greater expression in syncytiotrophoblast, consistent with KISS1 mRNA. Kisspeptin treatment inhibited the migratory potential of cytotrophoblast-like cells. Finally, while no difference was seen in KISS1 and KISS1R mRNA between term and pre-term placentas, we saw a difference in the relative expression of each gene pre-term. We also observed a positive correlation between KISS1 expression and maternal body mass index. Conclusions Our results indicate that kisspeptin may inhibit trophoblast invasion. Implications Further investigation is required to clarify specific regulatory mechanisms.
越来越多的证据表明,kisspeptin 信号在胎盘发育和功能中起作用。
本研究旨在利用三种实验模型阐明 kisspeptin 在滋养细胞侵袭和迁移中的作用。
首先,我们检查了 kisspeptin 受体(Kiss1r)敲除(KO)模型中的小鼠胎儿和胎盘。评估胎儿/胎盘重量和基因表达(定量聚合酶链反应)。其次,我们确定了 kisspeptin 对人滋养细胞(BeWo)细胞系的体外作用。第三,我们检查了来自足月和早产妊娠的人胎盘中的 KISS1 和 KISS1R 基因表达。
在 Kiss1r KO 和野生型小鼠之间,胎儿或胎盘重量没有差异。然而,在 Kiss1r KO 小鼠的胎盘绒毛区,滋养细胞侵袭标志物 Mmp2 mRNA 的表达更高。绒毛滋养细胞和合体滋养细胞的 BeWo 细胞模型表现出 kisspeptin 蛋白表达,合体滋养细胞中的表达更高,与 KISS1 mRNA 一致。Kisspeptin 处理抑制了滋养细胞样细胞的迁移潜力。最后,虽然在足月和早产胎盘中,KISS1 和 KISS1R mRNA 之间没有差异,但我们看到了每个基因在早产时的相对表达差异。我们还观察到 KISS1 表达与母体体重指数之间存在正相关。
我们的结果表明,kisspeptin 可能抑制滋养细胞侵袭。
需要进一步研究以阐明特定的调节机制。