Department of Neurobiology, David Geffen School of Medicine at UCLA, Los Angeles, Los Angeles, CA 90095, USA.
Department of OBGYN and Reproductive Sciences, University of California, San Diego, La Jolla, CA 92093, USA.
Endocrinology. 2021 Nov 1;162(11). doi: 10.1210/endocr/bqab161.
Kisspeptin, encoded by Kiss1, stimulates gonadotropin-releasing hormone neurons to govern reproduction. In female rodents, estrogen-sensitive kisspeptin neurons in the rostral anteroventral periventricular (AVPV) hypothalamus are thought to mediate estradiol (E2)-induced positive feedback induction of the preovulatory luteinizing hormone (LH) surge. AVPV kisspeptin neurons coexpress estrogen and progesterone receptors (PGRs) and are activated during the LH surge. While E2 effects on kisspeptin neurons have been well studied, progesterone's regulation of kisspeptin neurons is less understood. Using transgenic mice lacking PGR exclusively in kisspeptin cells (termed KissPRKOs), we previously demonstrated that progesterone action specifically in kisspeptin cells is essential for ovulation and normal fertility. Unlike control females, KissPRKO females did not generate proper LH surges, indicating that PGR signaling in kisspeptin cells is required for positive feedback. However, because PGR was knocked out from all kisspeptin neurons in the brain, that study was unable to determine the specific kisspeptin population mediating PGR action on the LH surge. Here, we used targeted Cre-mediated adeno-associated virus (AAV) technology to reintroduce PGR selectively into AVPV kisspeptin neurons of adult KissPRKO females, and tested whether this rescues occurrence of the LH surge. We found that targeted upregulation of PGR in kisspeptin neurons exclusively in the AVPV is sufficient to restore proper E2-induced LH surges in KissPRKO females, suggesting that this specific kisspeptin population is a key target of the necessary progesterone action for the surge. These findings further highlight the critical importance of progesterone signaling, along with E2 signaling, in the positive feedback induction of LH surges and ovulation.
Kisspeptin 由 Kiss1 编码,可刺激促性腺激素释放激素神经元以控制生殖。在雌性啮齿动物中,认为额前腹侧室旁核(AVPV)下丘脑中的雌激素敏感 kisspeptin 神经元介导雌二醇(E2)诱导的促黄体生成素(LH)峰前的正反馈诱导。AVPV kisspeptin 神经元共同表达雌激素和孕激素受体(PGRs),并在 LH 峰期间被激活。虽然已经对 E2 对 kisspeptin 神经元的作用进行了广泛研究,但孕激素对 kisspeptin 神经元的调节作用知之甚少。我们之前使用缺乏 kisspeptin 细胞中 PGR 的转基因小鼠(称为 KissPRKOs)表明,kisspeptin 细胞中孕激素的特定作用对于排卵和正常生育能力是必不可少的。与对照雌性不同,KissPRKO 雌性不会产生适当的 LH 峰,表明 kisspeptin 细胞中的 PGR 信号对于正反馈是必需的。然而,由于 PGR 从大脑中的所有 kisspeptin 神经元中被敲除,因此该研究无法确定介导 PGR 对 LH 峰作用的特定 kisspeptin 群体。在这里,我们使用靶向 Cre 介导的腺相关病毒(AAV)技术选择性地将 PGR 重新引入成年 KissPRKO 雌性的 AVPV kisspeptin 神经元,并测试了这是否可以挽救 LH 峰的发生。我们发现,仅在 AVPV 中 kisspeptin 神经元中靶向上调 PGR 足以恢复 KissPRKO 雌性中适当的 E2 诱导的 LH 峰,这表明该特定的 kisspeptin 群体是 LH 峰和排卵的正反馈诱导所必需的孕激素作用的关键靶标。这些发现进一步强调了孕激素信号与 E2 信号在 LH 峰和排卵的正反馈诱导中的重要性。