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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >Retinoic acid- and phorbol ester-induced neuronal differentiation down-regulates caveolin expression in GnRH neurons.
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Retinoic acid- and phorbol ester-induced neuronal differentiation down-regulates caveolin expression in GnRH neurons.

机译:维甲酸和佛波酯诱导的神经元分化下调GnRH神经元中的小窝蛋白表达。

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摘要

GN11 and GT1-7 are immortalized gonadotropin-releasing hormone-positive murine cell lines exhibiting the features of immature olfactory neurons and differentiated hypothalamic neurons, respectively. Using electron microscopy and biochemical assays (RT-PCR and immunoblotting) we determined the presence of numerous caveolae invaginations and of caveolin-1 and -2 mRNAs and proteins in GN11 cells, and their absence in GT1-7 cells. The lack of caveolins in GT1-7 cells might be due to the silencing of gene transcription caused by estrogen receptor alpha whose inhibitory activity in GN11 cells could be counter-balanced by co-expression of caveolin-permissive estrogen receptor beta. To test whether the unique expression of caveolins in GN11 cells is related to their immature state, we treated GN11 cells for 24-72 h with retinoic acid or phorbol ester. Both treatments led to neuronal differentiation of GN11 cells, as shown by emission of long neuritic processes, increased expression of growth cone-associated protein-43 and appearance of voltage-gated K+ and C2+ channel currents. Concurrently, caveolins 1 and 2, and estrogen receptor beta were down-regulated in differentiated GN11, whereas estrogen receptor alpha was unaffected by differentiation. We conclude that caveolin expression in GN11 neurons is down-regulated upon differentiation and up-regulated by estrogen receptor beta.
机译:GN11和GT1-7是永生的促性腺激素释放激素阳性小鼠细胞系,分别表现出不成熟的嗅觉神经元和分化的下丘脑神经元的特征。使用电子显微镜和生化分析(RT-PCR和免疫印迹),我们确定了GN11细胞中存在大量小窝内陷和小窝蛋白1和-2 mRNA和蛋白,而在GT1-7细胞中则不存在。 GT1-7细胞中空洞蛋白的缺乏可能是由于雌激素受体α导致基因转录沉默所致,其在GN11细胞中的抑制活性可能通过空洞性允许的空洞雌激素受体β的共表达来抵消。为了测试小窝蛋白在GN11细胞中的独特表达是否与它们的未成熟状态有关,我们用视黄酸或佛波酯处理了GN11细胞24-72小时。两种治疗均导致GN11细胞的神经元分化,如长神经突的释放,生长锥相关蛋白43的表达增加以及电压门控的K +和C2 +通道电流的出现所示。同时,在分化的GN11中小窝蛋白1和2,以及雌激素受体β被下调,而雌激素受体α不受分化的影响。我们得出的结论是,GN11神经元中的小窝蛋白表达在分化后被下调,并被雌激素受体β上调。

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