Kauffman Alexander S, Park Jin Ho, McPhie-Lalmansingh Anika A, Gottsch Michelle L, Bodo Cristian, Hohmann John G, Pavlova Maria N, Rohde Alex D, Clifton Donald K, Steiner Robert A, Rissman Emilie F
Department of Biochemistry and Molecular Genetics, University of Virginia, Charlottesville, Virginia 22908, USA.
J Neurosci. 2007 Aug 15;27(33):8826-35. doi: 10.1523/JNEUROSCI.2099-07.2007.
GPR54 is a G-protein-coupled receptor, which binds kisspeptins and is widely expressed throughout the brain. Kisspeptin-GPR54 signaling has been implicated in the regulation of pubertal and adulthood gonadotropin-releasing hormone (GnRH) secretion, and mutations or deletions of GPR54 cause hypogonadotropic hypogonadism in humans and mice. Other reproductive roles for kisspeptin-GPR54 signaling, including the regulation of developmental GnRH secretion or sexual behavior in adults, have not yet been explored. Using adult wild-type (WT) and GPR54 knock-out (KO) mice, we first tested whether kisspeptin-GPR54 signaling is necessary for male and female sexual behaviors. We found that hormone-replaced gonadectomized GPR54 KO males and females displayed appropriate gender-specific adult sexual behaviors. Next, we examined whether GPR54 signaling is required for proper display of olfactory-mediated partner preference behavior. Testosterone-treated WT males preferred stimulus females rather than males, whereas similarly treated WT females and GPR54 KO males showed no preference for either sex. Because olfactory preference is sexually dimorphic and organized during development by androgens, we assessed whether GPR54 signaling is essential for sexual differentiation of other sexually dimorphic traits. Interestingly, adult testosterone-treated GPR54 KO males displayed "female-like" numbers of tyrosine hydroxylase-immunoreactive and Kiss1 mRNA-containing neurons in the anteroventral periventricular nucleus and likewise possessed fewer motoneurons in the spino-bulbocavernosus nucleus than did WT males. Our findings indicate that kisspeptin-GPR54 signaling is not required for male or female copulatory behavior, provided there is appropriate adulthood hormone replacement. However, GPR54 is necessary for proper male-like development of several sexually dimorphic traits, likely by regulating GnRH-mediated androgen secretion during "critical windows" in perinatal development.
GPR54是一种G蛋白偶联受体,它能结合 kisspeptins,在整个大脑中广泛表达。Kisspeptin - GPR54信号通路与青春期及成年期促性腺激素释放激素(GnRH)分泌的调节有关,GPR54的突变或缺失会导致人类和小鼠出现低促性腺激素性性腺功能减退。Kisspeptin - GPR54信号通路的其他生殖作用,包括对成年期发育过程中GnRH分泌的调节或性行为的调控,尚未得到探索。我们使用成年野生型(WT)和GPR54基因敲除(KO)小鼠,首先测试了kisspeptin - GPR54信号通路对于雄性和雌性性行为是否必要。我们发现,经激素替代的去势GPR54 KO雄性和雌性表现出适当的性别特异性成年性行为。接下来,我们研究了GPR54信号通路对于嗅觉介导的伴侣偏好行为的正确表现是否必要。经睾酮处理的WT雄性偏好刺激雌性而非雄性,而同样处理的WT雌性和GPR54 KO雄性对两种性别均无偏好。由于嗅觉偏好具有性别二态性,且在发育过程中由雄激素组织形成,我们评估了GPR54信号通路对于其他性别二态性特征的性分化是否至关重要。有趣的是,成年经睾酮处理的GPR54 KO雄性在室旁核前腹侧中酪氨酸羟化酶免疫反应阳性和含Kiss1 mRNA的神经元数量呈现“雌性样”,并且与WT雄性相比,其球海绵体核中的运动神经元数量也更少。我们的研究结果表明,如果有适当的成年期激素替代,kisspeptin - GPR54信号通路对于雄性或雌性交配行为并非必需。然而,GPR54对于几种性别二态性特征的正常雄性样发育是必要的,这可能是通过在围产期发育的“关键窗口”期间调节GnRH介导的雄激素分泌来实现的。