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Kisspeptin-10

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

Quick Stats
Studies 877
Trials 47
Score 2
2022 pubmed 12 citations

Kisspeptin-10 Promotes Progesterone Synthesis in Bovine Ovarian Granulosa Cells via Downregulation of microRNA-1246.

Guo. Lewei L; Xu. Haoran H; Li. Yajun Y; Liu. Hongyu H; Zhao. Jing J; Lu. Wenfa W; Wang. Jun J

Key Findings

  • Kisspeptin-10 treatment for 24 hours raises progesterone levels and the expression of the steroid‑making gene StAR in bovine granulosa cells.
  • UTR.",

Practical Outcomes

  • The study suggests kisspeptin‑10 can influence hormone production by targeting microRNA pathways, which might be of interest for future fertility or hormone‑balancing strategies. However, the work is limited to cow cells and does not provide dosage guidance or safety data for humans, so it’s not yet ready for direct self‑experimentation.

Summary

Researchers found that the peptide kisspeptin-10 can boost progesterone production in cow ovarian cells by lowering a tiny RNA molecule (miR‑1246) that normally blocks a key hormone‑making protein called StAR. When miR‑1246 is reduced, more cholesterol gets moved into the cells, leading to more progesterone.

Abstract

The objective of this study was to clarify the effect of kisspeptin-10 (kp-10) on the synthesis of progesterone (P4) in bovine granulosa cells (BGCs) and its mechanisms via microRNA 1246 (miR-1246). According to the results, we found that treating with kp-10 for 24 h could increase P4 level, the mRNA expression of the steroidogenesis-related gene <i>steroidogenic acute regulatory protein</i> (StAR), free cholesterol content, and decrease miR-1246 expression in BGCs. Overexpression of miR-1246 significantly inhibited P4 synthesis, StAR mRNA expression, and free cholesterol content in BGCs, whereas underexpression of miR-1246 significantly reversed this effect in BGCs. Additionally, overexpression of miR-1246 counteracted the accelerative effect of kp-10 on P4 synthesis, StAR mRNA expression, and free cholesterol content in BGCs. Conversely, underexpression of miR-1246 enhanced the accelerative effect of kp-10 on P4 synthesis, StAR mRNA expression, and free cholesterol content in BGCs. Meanwhile, results of dual-luciferase reporter assays indicated that miR-1246 targeted the 3'UTR of StAR in BGCs. These results demonstrated that kp-10 induced P4 synthesis in BGCs by promoting free cholesterol transport via regulating expression of miR-1246/StAR.

Study Information

Provider

pubmed

Year

2022

Date

2022-02-03T00:00:00.000Z

DOI

10.3390/genes13020298

Citations

12

References

45