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皮质类固醇对大鼠神经元中盐皮质激素受体基因的转录诱导作用。

Transcriptional induction of rat mineralocorticoid receptor gene in neurones by corticosteroids.

作者信息

Castrén M, Trapp T, Berninger B, Castrén E, Holsboer F

机构信息

Department of Neuroendocrinology, Max-Planck-Institute of Psychiatry, Munich, Germany.

出版信息

J Mol Endocrinol. 1995 Jun;14(3):285-93. doi: 10.1677/jme.0.0140285.

Abstract

We investigated the mechanisms by which corticosteroids regulate the expression of the mineralocorticoid receptor (MR) in neurones. Aldosterone and dexamethasone produced a dose-dependent increase of MR and mRNA levels in cultured primary hippocampal neurones. Transient transfection of neuroblastoma cells showed that corticosteroids directly activate the rat MR promoter, indicating that the steroid-induced increase in the MR mRNA concentration is at least partially transcriptional. Progressive 5' deletions of the MR promoter sequence revealed that the promoter induction cannot be assigned to a single element. An oligonucleotide comprising a consensus half-glucocorticoid responsive element located at -319 bp in the MR promoter stimulated the corticosteroid-induced activation of the heterologous promoter. Cloning three of these enhancers in tandem greatly potentiated the responses to glucocorticoids and mineralocorticoids, suggesting that although this element is a weak enhancer it can, in combination with other enhancer elements, induce MR gene expression by both types of corticosteroid receptors.

摘要

我们研究了皮质类固醇调节神经元中盐皮质激素受体(MR)表达的机制。醛固酮和地塞米松使原代培养海马神经元中的MR及mRNA水平呈剂量依赖性增加。神经母细胞瘤细胞的瞬时转染表明,皮质类固醇直接激活大鼠MR启动子,提示类固醇诱导的MR mRNA浓度增加至少部分是转录性的。MR启动子序列的逐步5'缺失显示,启动子诱导不能归因于单一元件。包含位于MR启动子-319 bp处的共有半糖皮质激素反应元件的寡核苷酸刺激了皮质类固醇诱导的异源启动子激活。将三个此类增强子串联克隆极大地增强了对糖皮质激素和盐皮质激素的反应,表明尽管该元件是一个弱增强子,但它可与其他增强子元件结合,通过两种类型的皮质类固醇受体诱导MR基因表达。

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