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维甲酸和佛波酯诱导的神经元分化下调促性腺激素释放激素(GnRH)神经元中的小窝蛋白表达。

Retinoic acid- and phorbol ester-induced neuronal differentiation down-regulates caveolin expression in GnRH neurons.

作者信息

D'Orlando Cristina, Guzzi Francesca, Gravati Marta, Biella Gerardo, Toselli Mauro, Meneveri Raffaella, Barisani Donatella, Parenti Marco

机构信息

Department of Experimental Medicine, University of Milano-Bicocca, Monza, Italy.

出版信息

J Neurochem. 2008 Mar;104(6):1577-87. doi: 10.1111/j.1471-4159.2007.05109.x. Epub 2007 Nov 5.

Abstract

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.

摘要

GN11和GT1 - 7是永生化的促性腺激素释放激素阳性小鼠细胞系,分别表现出未成熟嗅觉神经元和分化的下丘脑神经元的特征。通过电子显微镜和生化分析(逆转录聚合酶链反应和免疫印迹法),我们确定GN11细胞中存在大量小窝内陷以及小窝蛋白 - 1和 - 2的信使核糖核酸及蛋白质,而GT1 - 7细胞中则没有。GT1 - 7细胞中小窝蛋白的缺失可能是由于雌激素受体α导致的基因转录沉默,而在GN11细胞中,雌激素受体β的共表达可以抵消其抑制活性。为了测试GN11细胞中小窝蛋白的独特表达是否与其未成熟状态有关,我们用视黄酸或佛波酯处理GN11细胞24至72小时。两种处理均导致GN11细胞发生神经元分化,表现为长出长长的神经突、生长相关蛋白 - 43的表达增加以及电压门控钾离子和钙离子通道电流的出现。同时,在分化的GN11细胞中,小窝蛋白1和2以及雌激素受体β的表达下调,而雌激素受体α不受分化影响。我们得出结论,GN11神经元中的小窝蛋白表达在分化时下调,并由雌激素受体β上调。

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