Interaction between kisspeptin and adenylate cyclase-activating polypeptide 1 on the expression of pituitary gonadotropin subunits: a study using mouse pituitary lbetaT2 cells.
Mijiddorj. Tselmeg T; Kanasaki. Haruhiko H; Oride. Aki A; Hara. Tomomi T; Sukhbaatar. Unurjargal U; Tumurbaatar. Tuvshintugs T; Kyo. Satoru S
Key Findings
- Kisspeptin-10 increases promoter activity of LH and FSH subunit genes in pituitary cells, comparable to GnRH.
- Co‑stimulation with ADCYAP1 further amplifies the expression of these gonadotropin subunits.
- Kisspein-10 up‑regulates its own receptor (Adcyap1r), potentially enhancing its signaling capacity.
Practical Outcomes
- For biohackers, this suggests kisspeptin could be a tool to influence reproductive hormones without relying solely on GnRH pathways, but the evidence is limited to mouse cells in a dish. No dosage, safety, or human efficacy data are provided, so any real‑world protocol would be speculative at this stage.
Summary
The study shows that kisspeptin-10 can directly boost the production of hormone subunits that make up LH and FSH in mouse pituitary cells, acting similarly to GnRH. When combined with another peptide, ADCYAP1, the effect is even stronger. Kisspeptin also raises the levels of its own receptor, suggesting a feedback loop.
Abstract
We examined direct effect of kisspeptin on pituitary gonadotrophs. Kisspeptin-10 (KP10) significantly increased the promoter activities of the gonadotropin subunits, common alpha-glycoprotein (Cga), luteinizing hormone beta (Lhb), and follicle-stimulatinghormone beta (Fshb) in LbetaT2 cells overexpressing kisspeptin receptor (Kiss1r). KP10 and gonadotropin-releasing hormone (GnRH) increased gonadotropin subunit levels to similar degrees and combined treatment with GnRH and KP10 did not potentiate their individual effects. Adenylate cyclase-activating polypeptide 1 (ADCYAP1) also stimulates all three gonadotropin subunits. When cells were stimulated with both KP10 and ADCYAP1, expression of gonadotropin subunits was further increased compared to KP10 or ADCYAP1 alone. KP10 and GnRH dramatically increased serum response element (Sre) promoter levels but only slightly increased cAMP response element (Cre) promoter levels. Combined stimulation with KP10 and GnRH further increased Sre promoter levels. In contrast, ADCYAP1 slightly increased Sre promoter expression but did not modify the effect of KP10. However, ADCYAP1 increased Cre promoter to greater levels than KP10 alone, and combined treatment with KP10 and ADCYAP1 further increased Cre promoter expression. KP10 increased the expression of ADCYAP1 type I receptor (Adcyap1r) and the basal activity of the Cga promoter was increased at a higher Adcyap1r transfection level. The KP10-induced fold increase in all three gonadotropin subunit promoters was not altered by transfection with a higher amount of Adcyap1r vector. Our findings using model cells show that distinct signaling activation by ADCYAP1 potentiates the action of KP10. We also found that KP10 increases Adcyap1r expression.
Study Information
pubmed
2017
2017-05-01T00:00:00.000Z
10.1093/biolre/iox030
9
45