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Kisspeptin-10

KP-10, Metastin (45-54), Kisspeptin-10 (human), KiSS-1

Quick Stats
Studies 877
Trials 47
Score 1
2024 pubmed

The role of placental kisspeptin in trophoblast invasion and migration: an assessment in <i>Kiss1r</i> knockout mice, BeWo cell lines and human term placenta.

Panting. E N EN; Weight. J H JH; Sartori. J A JA; Coall. D A DA; Smith. J T JT

Key Findings

  • Mice lacking the kisspeptin receptor had higher levels of the invasion‑related gene Mmp2 in the placenta, but no change in fetal or placental weight.
  • Human placental cells (BeWo) produce kisspeptin, especially in the syncytiotrophoblast layer, and adding kisspeptin reduces the migration ability of cytotrophoblast‑like cells.
  • KISS1 gene expression in human placentas correlates positively with maternal BMI, though overall KISS1/KISS1R levels are similar between term and pre‑term births.

Practical Outcomes

  • For most biohackers, this research doesn’t translate into a usable supplement or protocol. It suggests kisspeptin influences cell invasion in the placenta, but there’s no evidence it affects adult metabolism, body composition, or performance. Until more human data emerge, there’s no actionable step to take with kisspeptin‑10 for longevity or health optimization.

Summary

The study shows that kisspeptin, a hormone usually linked to reproduction, can slow down the movement of certain placenta cells in mice and human cell models. It doesn't change fetal or placental size, but it does affect genes tied to cell invasion and is linked to the mother's body weight.

Abstract

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.

Study Information

Provider

pubmed

Year

2024

DOI

10.1071/rd23230