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Kisspeptin-GPR54 信号在小鼠的一氧化氮合成神经元中参与了下丘脑对排卵的控制。

Kisspeptin-GPR54 signaling in mouse NO-synthesizing neurons participates in the hypothalamic control of ovulation.

机构信息

Inserm, Jean-Pierre Aubert Research Center, U837, Development and Plasticity of the Postnatal Brain, Institut Fédératif de Recherche 114, France.

出版信息

J Neurosci. 2012 Jan 18;32(3):932-45. doi: 10.1523/JNEUROSCI.4765-11.2012.

Abstract

Reproduction is controlled in the brain by a neural network that drives the secretion of gonadotropin-releasing hormone (GnRH). Various permissive homeostatic signals must be integrated to achieve ovulation in mammals. However, the neural events controlling the timely activation of GnRH neurons are not completely understood. Here we show that kisspeptin, a potent activator of GnRH neuronal activity, directly communicates with neurons that synthesize the gaseous transmitter nitric oxide (NO) in the preoptic region to coordinate the progression of the ovarian cycle. Using a transgenic Gpr54-null IRES-LacZ knock-in mouse model, we demonstrate that neurons containing neuronal NO synthase (nNOS), which are morphologically associated with kisspeptin fibers, express the kisspeptin receptor GPR54 in the preoptic region, but not in the tuberal region of the hypothalamus. The activation of kisspeptin signaling in preoptic neurons promotes the activation of nNOS through its phosphorylation on serine 1412 via the AKT pathway and mimics the positive feedback effects of estrogens. Finally, we show that while NO release restrains the reproductive axis at stages of the ovarian cycle during which estrogens exert their inhibitory feedback, it is required for the kisspeptin-dependent preovulatory activation of GnRH neurons. Thus, interactions between kisspeptin and nNOS neurons may play a central role in regulating the hypothalamic-pituitary-gonadal axis in vivo.

摘要

生殖是由一个神经网络控制的,该网络驱动促性腺激素释放激素 (GnRH) 的分泌。各种允许的稳态信号必须整合在一起,才能在哺乳动物中实现排卵。然而,控制 GnRH 神经元适时激活的神经事件还不完全清楚。在这里,我们表明,促性腺激素释放激素神经元活性的有效激活剂 kisspeptin,直接与在视前区合成气态递质一氧化氮 (NO) 的神经元进行通讯,以协调卵巢周期的进展。使用 Gpr54 缺失型 IRES-LacZ 敲入小鼠模型,我们证明含有神经元型一氧化氮合酶 (nNOS) 的神经元,其形态与 kisspeptin 纤维相关,在视前区表达 kisspeptin 受体 GPR54,但不在下丘脑的结节区表达。视前神经元中 kisspeptin 信号的激活通过 AKT 途径促进 nNOS 上丝氨酸 1412 的磷酸化,从而模拟雌激素的正反馈效应。最后,我们表明,虽然在雌激素发挥抑制性反馈作用的卵巢周期阶段,NO 释放会抑制生殖轴,但它对于 kisspeptin 依赖性 GnRH 神经元的促排卵激活是必需的。因此,kisspeptin 和 nNOS 神经元之间的相互作用可能在体内调节下丘脑-垂体-性腺轴中发挥核心作用。

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