Kauffman Alexander S
Department of Physiology & Biophysics, Health Sciences Building, Box 357290, University of Washington, Seattle, WA 98195, United States.
Peptides. 2009 Jan;30(1):83-93. doi: 10.1016/j.peptides.2008.06.014. Epub 2008 Jul 3.
The nervous system (both central and peripheral) is anatomically and physiologically differentiated between the sexes, ranging from gender-based differences in the cerebral cortex to motoneuron number in the spinal cord. Although genetic factors may play a role in the development of some sexually differentiated traits, most identified sex differences in the brain and behavior are produced under the influence of perinatal sex steroid signaling. In many species, the ability to display an estrogen-induced luteinizing hormone (LH) surge is sexually differentiated, yet the specific neural population(s) that allows females but not males to display such estrogen-mediated "positive feedback" has remained elusive. Recently, the Kiss1/kisspeptin system has been implicated in generating the sexually dimorphic circuitry underlying the LH surge. Specifically, Kiss1 gene expression and kisspeptin protein levels in the anteroventral periventricular (AVPV) nucleus of the hypothalamus are sexually differentiated, with females displaying higher levels than males, even under identical hormonal conditions as adults. These findings, in conjunction with accumulating evidence implicating kisspeptins as potent secretagogues of gonadotropin-releasing hormone (GnRH), suggest that the sex-specific display of the LH surge (positive feedback) reflects sexual differentiation of AVPV Kiss1 neurons. In addition, developmental kisspeptin signaling via its receptor GPR54 appears to be critical in males for the proper sexual differentiation of a variety of sexually dimorphic traits, ranging from complex social behavior to specific forebrain and spinal cord neuronal populations. This review discusses the recent data, and their implications, regarding the bi-directional relationship between the Kiss1 system and the process of sexual differentiation.
神经系统(包括中枢神经系统和外周神经系统)在解剖学和生理学上存在性别差异,范围从大脑皮层基于性别的差异到脊髓运动神经元数量的差异。尽管遗传因素可能在某些性别分化特征的发育中起作用,但在大脑和行为中确定的大多数性别差异是在围产期性类固醇信号的影响下产生的。在许多物种中,显示雌激素诱导的促黄体生成素(LH)激增的能力存在性别差异,然而,允许雌性而非雄性表现出这种雌激素介导的“正反馈”的特定神经群体仍然难以捉摸。最近,Kiss1/ kisspeptin系统被认为与产生LH激增背后的性别二态性神经回路有关。具体而言,下丘脑腹侧室旁前部(AVPV)核中的Kiss1基因表达和kisspeptin蛋白水平存在性别差异,即使在成年后处于相同激素条件下,雌性的水平也高于雄性。这些发现,连同越来越多的证据表明kisspeptins是促性腺激素释放激素(GnRH)的有效促分泌素,表明LH激增(正反馈)的性别特异性表现反映了AVPV Kiss1神经元的性别分化。此外,发育过程中通过其受体GPR54的kisspeptin信号传导,对于雄性各种性别二态性特征的正确性别分化似乎至关重要,这些特征从复杂的社会行为到特定的前脑和脊髓神经元群体不等。本综述讨论了关于Kiss1系统与性别分化过程之间双向关系的最新数据及其意义。