首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Regulation of dendritic spine density in cultured rat hippocampal neurons by steroid hormones.
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Regulation of dendritic spine density in cultured rat hippocampal neurons by steroid hormones.

机译:类固醇激素对培养的大鼠海马神经元中树突棘密度的调节。

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The effects of gonadal steroid hormones on dendritic spines were studied in hippocampal neurons that were dissociated and grown in culture for 2-3 weeks. Exposure to estradiol caused up to a twofold increase in dendritic spine density in these neurons. The effect of estradiol was stereospecific and blocked by the steroid antagonist tamoxifen. The estradiol-induced rise in spine density was blocked by the NMDA antagonist APV, but not by the AMPA/KA antagonist DNQX. The estradiol-induced rise in spine density was blocked by the serine/threonine kinase inhibitor H7, but not by the tyrosine kinase inhibitor genestein, and was partially mimicked by PMA, an activator of protein kinase C. Estradiol also caused an increase in the fluorescence intensity of synaptophysin-immunoreactive terminals, corresponding to presynaptic boutons. Finally, estradiol caused a rise in [Ca]i reactivity of the cultured neurons to topical application of glutamate. These studies are the first to examine receptor and second messenger regulation of dendritic spines, and they illustrate the viability of cultured neurons as a powerful test system to address issues related to the regulation of dendritic spine maturation.
机译:在分离并培养2-3周的海马神经元中研究了性腺类固醇激素对树突棘的影响。暴露于雌二醇可导致这些神经元的树突棘密度增加两倍。雌二醇的作用是立体定向的,并被类固醇拮抗剂他莫昔芬阻断。雌二醇诱导的脊柱密度升高被NMDA拮抗剂APV阻止,但未被AMPA / KA拮抗剂DNQX阻止。雌二醇诱导的脊柱密度升高被丝氨酸/苏氨酸激酶抑制剂H7阻止,但未被酪氨酸激酶抑制剂Genestein阻止,并且部分被蛋白激酶C的活化剂PMA模仿。雌二醇还引起荧光增强突触素免疫反应终末的强度,对应于突触前的按钮。最后,雌二醇引起培养的神经元对谷氨酸局部施用的[Ca]反应性升高。这些研究是首次检查树突棘的受体和第二信使调节,并且它们说明了培养的神经元作为解决与树突棘成熟的调节有关的问题的强大测试系统的可行性。

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