Centre for Neuroendocrinology, Departments of Physiology, University of Otago, Dunedin 9054, New Zealand.
Front Neuroendocrinol. 2010 Jul;31(3):259-69. doi: 10.1016/j.yfrne.2010.05.005. Epub 2010 Jun 2.
The gonadotropin-releasing hormone (GnRH) neurons represent the key output cells of the neuronal network controlling fertility. Intracellular calcium ion concentration (Ca(2+)) is likely to be a key signaling tool used by GnRH neurons to regulate and co-ordinate multiple cell processes. This review examines the dynamics and control of Ca(2+) in GT1 cells, embryonic GnRH neurons in the nasal placode culture, and adult GnRH neurons in the acute brain slice preparation. GnRH neurons at all stages of development display spontaneous Ca(2+) transients driven, primarily, by their burst firing. However, the intracellular mechanisms generating Ca(2+) transients, and the control of Ca(2+) by neurotransmitters, varies markedly across the different developmental stages. The functional roles of Ca(2+) transients are beginning to be unraveled with one key action being that of regulating the dynamics of GnRH neuron burst firing.
促性腺激素释放激素 (GnRH) 神经元是控制生育能力的神经元网络的关键输出细胞。细胞内钙离子浓度 (Ca(2+)) 很可能是 GnRH 神经元用来调节和协调多种细胞过程的关键信号工具。本综述检查了 GT1 细胞、鼻基板培养中的胚胎 GnRH 神经元和急性脑切片制备中的成年 GnRH 神经元中 Ca(2+) 的动力学和控制。在发育的所有阶段,GnRH 神经元都显示出由其爆发放电驱动的自发 Ca(2+) 瞬变。然而,产生 Ca(2+) 瞬变的细胞内机制以及神经递质对 Ca(2+) 的控制在不同的发育阶段有很大的差异。Ca(2+) 瞬变的功能作用开始被揭示,其中一个关键作用是调节 GnRH 神经元爆发放电的动力学。