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Interaction of sex chromosome complement, gonadal hormones and neuronal steroid synthesis on the sexual differentiation of mammalian neurons

机译:性染色体补体,性腺激素和神经元类固醇合成对哺乳动物神经元的性分化的相互作用

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Female mouse hippocampal and hypothalamic neurons growing in vitro show a faster development of neurites than male mouse neurons. This sex difference in neuritogenesis is determined by higher expression levels of the neuritogenic factor neurogenin 3 in female neurons. Experiments with the four core genotype mouse model, in which XX and XY animals with male gonads and XX and XY animals with female gonads are generated, indicate that higher levels of neurogenin 3 in developing neurons are determined by the presence of the XX chromosome complement. Female XX neurons express higher levels of estrogen receptors than male XY neurons. In female XX neurons, neuronal derived estradiol increases neurogenin 3 expression and neuritogenesis. In contrast, neuronal-derived estradiol is not able to upregulate neurogenin 3 in male XY neurons, resulting in decreased neuritogenesis compared to female neurons. However, exogenous testosterone increases neurogenin 3 expression and neuritogenesis in male XY neurons. These findings suggest that sex differences in neuronal development are determined by the interaction of sex chromosomes, neuronal derived estradiol and gonadal hormones.
机译:体外生长的雌性小鼠海马和下丘脑神经元显得比男鼠神经元更快速地发展。神经发生的这种性别差异是通过雌性神经元中神经源性因子神经原因3的较高表达水平确定的。用四种核心基因型小鼠模型进行实验,其中产生具有雄性腺和XX和XY动物的XX和XY动物,表明通过XX染色体互补的存在来确定XX发育神经元中的高水平神经元素3。雌性XX神经元表达比男性XY神经元更高水平的雌激素受体。在雌性XX神经元中,神经元衍生的雌二醇增加神经原素3表达和神经发生。相反,神经元衍生的雌二醇不能在雄性XY神经元中上调神经原素3,导致与雌性神经元相比的神经发生减少。然而,外源性睾酮增加了雄性XY神经元的神经原因3表达和神经发生。这些发现表明,神经元发展的性差异由性染色体,神经元衍生的雌二醇和雌二醇激素的相互作用决定。

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