Weiner R I, Wetsel W, Goldsmith P, Martinez de la Escalera G, Windle J, Padula C, Choi A, Negro-Vilar A, Mellon P
Reproductive Endocrinology Center, University of California, San Francisco 94143.
Front Neuroendocrinol. 1992 Apr;13(2):95-119.
Gonadotropin-releasing hormone (GnRH) cell lines were developed by genetically targeted tumorigenesis in transgenic mice. The cell lines designated GT1 cells have a neuronal phenotype, express neuronal but not glial markers and express the GnRH gene at high levels. The GnRH prohormone is processed in the cells to multiple molecular forms including biologically active GnRH and GnRH-associated peptide. Basal secretion of GnRH from the cells is regulated in part by fast Na+ channels necessary for propagated action potentials. In many instances, basal GnRH release is pulsatile with an interpulse frequency similar to that seen in castrated rodents, suggesting that GnRH neurons are the pulse generator and are capable of synchronizing their secretion in vitro. The secretion of GnRH is stimulated by depolarization and by the neurotransmitter norepinephrine. In related studies we have demonstrated that expression of Simian virus 40 T antigen in GnRH neurons of transgenic mice leads to hypothalamic hypogonadism due to the inability of GnRH nerve terminals to organize in the median eminence. These findings support the use of genetically-directed tumorigenesis to establish highly differentiated GnRH neuronal cell lines that are a valuable model to study the cell biology and regulation of the neurons.
促性腺激素释放激素(GnRH)细胞系是通过转基因小鼠中的基因靶向肿瘤发生而建立的。命名为GT1细胞的细胞系具有神经元表型,表达神经元标志物而非胶质细胞标志物,并高水平表达GnRH基因。GnRH前体激素在细胞中被加工成多种分子形式,包括生物活性GnRH和GnRH相关肽。细胞中GnRH的基础分泌部分受传播动作电位所需的快速Na+通道调节。在许多情况下,基础GnRH释放呈脉冲式,脉冲间期频率与去势啮齿动物相似,这表明GnRH神经元是脉冲发生器,并且能够在体外同步其分泌。GnRH的分泌受去极化和神经递质去甲肾上腺素刺激。在相关研究中,我们已经证明,转基因小鼠GnRH神经元中猿猴病毒40 T抗原的表达会导致下丘脑性腺功能减退,原因是GnRH神经末梢无法在正中隆起中组织起来。这些发现支持利用基因导向的肿瘤发生来建立高度分化的GnRH神经元细胞系,这是研究神经元细胞生物学和调节的有价值模型。