胎盘kisspeptin在滋养层侵入和迁移中的作用:Kiss1r基因敲除小鼠、BeWo细胞系和人类足月胎盘的评估。

IF 2.1
E N Panting, J H Weight, J A Sartori, D A Coall, J T Smith
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引用次数: 0

摘要

背景 越来越多的证据表明,吻合素信号与胎盘的发育和功能有关。目的 本研究旨在利用三种实验模型阐明吻肽在滋养细胞侵袭和迁移中的作用。方法 首先,我们在kisspeptin受体(Kiss1r)敲除(KO)模型中检测了小鼠胎儿和胎盘。评估了胎儿/胎盘重量和基因表达(定量聚合酶链反应)。其次,我们在体外测定了Kisspeptin对人类滋养细胞(BeWo)细胞系的影响。第三,我们检测了足月妊娠和早产妊娠人类胎盘中 KISS1 和 KISS1R 基因的表达。主要结果 Kiss1r KO 小鼠和野生型小鼠的胎儿或胎盘重量没有差异。然而,Kiss1r KO小鼠胎盘迷宫区滋养层侵入标记物Mmp2 mRNA的表达量更高。绒毛细胞滋养层细胞和合胞滋养层细胞的BeWo细胞模型显示了Kisspeptin蛋白的表达,其中合胞滋养层细胞的表达量更大,这与KISS1 mRNA一致。Kisspeptin 处理抑制了类细胞的迁移潜力。最后,虽然KISS1和KISS1R mRNA在足月胎盘和早产胎盘中没有差异,但我们发现每个基因在早产胎盘中的相对表达量存在差异。我们还观察到 KISS1 表达与母体体重指数呈正相关。结论 我们的研究结果表明,kisspeptin 可抑制滋养细胞的侵入。启示 需要进一步研究以明确具体的调控机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of placental kisspeptin in trophoblast invasion and migration: an assessment in Kiss1r knockout mice, BeWo cell lines and human term placenta.

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.

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