Estrogen and Progesterone Integration in an in vitro Model of RP3V Kisspeptin Neurons

• DOI: 10.1159/000471878
• Publication Date: 2017-04-07T02:40:49Z
• Authors: Melinda A. Mittel...; Angela M. Wong; Paul E. Micevych
• Keywords: Estrogen positive feedback; 1.1 Normal biological development and functioning; Physiological; Clinical Sciences; Hypothalamus; Clinical sciences; Feedback; Progesterone receptor; Cell Line; Endocrinology & Metabolism; Mice; 03 medical and health sciences; Conditioned; Underpinning research; Receptors; Animals; Progesterone; ERα; Feedback, Physiological; Mitogen-Activated Protein Kinase 1; Neurons; Kisspeptins; 0303 health sciences; Mitogen-Activated Protein Kinase 3; Biomedical and Clinical Sciences; mPR; Contraception/Reproduction; Neurosciences; Estrogen Receptor alpha; Estrogens; Estrogen; MAPK; Coculture Techniques; Culture Media; ER alpha; src-Family Kinases; Reproductive Medicine; Astrocytes; Culture Media, Conditioned; Protein Biosynthesis; Biological psychology; Female; Receptors, Progesterone; Src

Positive feedback on gonadotropin release requires not only estrogen but also progesterone to activate neural circuits. In rodents, ovarian estradiol (E2) stimulates progesterone synthesis in hypothalamic astrocytes (neuroP), needed for the luteinizing hormone (LH) surge. Kisspeptin (kiss) neurons are the principal stimulators of gonadotropin-releasing hormone neurons, and disruption of kiss signaling abrogates the LH surge. Similarly, blocking steroid synthesis in the hypothalamus or deleting classical progesterone receptor (PGR) selectively in kiss neurons prevents the LH surge. These results suggest a synergistic action of E2 and progesterone in kiss neurons to affect gonadotropin release. The mHypoA51, immortalized kiss-expressing neuronal cell line derived from adult female mice, is a tractable model for examining integration of steroid signaling underlying estrogen positive feedback. Here, we report that kiss neurons in vitro integrate E2 and progesterone signaling to increase levels of kiss translation and release. mHypoA51 neurons expressed nonclassical membrane progesterone receptors (mPRα and mPRβ) and E2-inducible PGR, required for progesterone-augmentation of E2-induced kiss expression. With astrocyte-conditioned media or in mHypoA51-astrocyte co-culture, neuroP augmented stimulatory effects of E2 on kiss protein. Progesterone activation of classical, membrane-localized PGR led to activation of MAPK and Src kinases. Importantly, progesterone or Src activation induced release of kiss from E2-primed mHypoA51 neurons. Consistent with previous studies, the present results provide compelling evidence that the interaction of E2 and progesterone stimulates kiss expression and release. Further, these results demonstrate a mechanism though which peripheral E2 may prime kiss neurons to respond to neuroP, mediating estrogen positive feedback.