Kisspeptin signaling in astrocytes modulates the reproductive axis.
Torres. Encarnacion E; Pellegrino. Giuliana G; Granados-Rodríguez. Melissa M; Fuentes-Fayos. Antonio C AC; Velasco. Inmaculada I; Coutteau-Robles. Adrian A; Legrand. Amandine A; Shanabrough. Marya M; Perdices-Lopez. Cecilia C; Leon. Silvia S; Yeo. Shel H SH; Manchishi. Stephen M SM; Sánchez-Tapia. Maria J MJ; Navarro. Victor M VM; Pineda. Rafael R; Roa. Juan J; Naftolin. Frederick F; Argente. Jesús J; Luque. Raúl M RM; Chowen. Julie A JA; Horvath. Tamas L TL; Prevot. Vincent V; Sharif. Ariane A; Colledge. William H WH; Tena-Sempere. Manuel M; Romero-Ruiz. Antonio A
Key Findings
- Kisspeptin receptors (KISS1R) are present on astrocytes in mouse and human brain tissue.
- Activating these receptors changes astrocyte signaling pathways and alters genes involved in prostaglandin E2 production.
- Removing KISS1R from astrocytes disrupts normal hormone (LH) pulses and impairs reproductive responses to metabolic stress such as a high‑fat diet.
Practical Outcomes
- The study suggests kisspeptin’s effects on fertility and metabolism aren’t limited to neurons; astrocytes also play a role. While this doesn’t yet translate into a dosing protocol, it hints that targeting kisspeptin pathways could one day help modulate reproductive hormones or mitigate diet‑induced reproductive issues. For now, it’s mainly a mechanistic insight rather than a direct actionable strategy.
Summary
Scientists found that kisspeptin, a hormone known for controlling reproduction, also talks to brain support cells called astrocytes. This extra communication helps fine‑tune the release of reproductive hormones and changes how the body reacts to a high‑fat diet, especially in females.
Abstract
Reproduction is safeguarded by multiple, often cooperative, regulatory networks. Kisspeptin signaling, via KISS1R, plays a fundamental role in reproductive control, primarily by regulation of hypothalamic GnRH neurons. We disclose herein a pathway for direct kisspeptin actions in astrocytes that contributes to central reproductive modulation. Protein-protein interaction and ontology analyses of hypothalamic proteomic profiles after kisspeptin stimulation revealed that glial/astrocyte markers are regulated by kisspeptin in mice. This glial-kisspeptin pathway was validated by the demonstrated expression of Kiss1r in mouse astrocytes in vivo and astrocyte cultures from humans, rats, and mice, where kisspeptin activated canonical intracellular signaling-pathways. Cellular coexpression of Kiss1r with the astrocyte markers GFAP and S100-β occurred in different brain regions, with higher percentage in Kiss1- and GnRH-enriched areas. Conditional ablation of Kiss1r in GFAP-positive cells in the G-KiR-KO mouse altered gene expression of key factors in PGE2 synthesis in astrocytes and perturbed astrocyte-GnRH neuronal appositions, as well as LH responses to kisspeptin and LH pulsatility, as surrogate marker of GnRH secretion. G-KiR-KO mice also displayed changes in reproductive responses to metabolic stress induced by high-fat diet, affecting female pubertal onset, estrous cyclicity, and LH-secretory profiles. Our data unveil a nonneuronal pathway for kisspeptin actions in astrocytes, which cooperates in fine-tuning the reproductive axis and its responses to metabolic stress.
Study Information
pubmed
2024
2024-06-11T00:00:00.000Z
10.1172/jci172908