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首页> 外文期刊>The Journal of Steroid Biochemistry and Molecular Biology >Steroid hormones upregulate rat angiotensin II type 1A receptor gene: role of glucocorticoid responsive elements in rat angiotensin II type 1A promoter.
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Steroid hormones upregulate rat angiotensin II type 1A receptor gene: role of glucocorticoid responsive elements in rat angiotensin II type 1A promoter.

机译:类固醇激素上调大鼠血管紧张素II 1A型受体基因:糖皮质激素应答元件在大鼠血管紧张素II 1A型启动子中的作用。

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摘要

The transcription of the rat angiotensin II type 1A receptor gene is stimulated by glucocorticoids. To clarify the molecular mechanism for glucocorticoid action in rat vascular smooth muscle cells, we investigated the effects of dexamethasone on the promoter activity of the angiotensin II type 1A receptor by using promoter/luciferase reporter gene constructs and heterologous context constructs (containing the thymidine kinase promoter) in transfected vascular smooth muscle cells. There are three putative glucocorticoid responsive elements in the promoter. However, only one glucocorticoid responsive element was found to respond to dexamethasone (1 microM). The region was located at positions, -756 to -770 bp upstream of the transcription initiation site. A glucocorticoid antagonist, RU38486, completely blocked the induction by dexamethasone, suggesting that the glucocorticoid responsive element was functional through a specific glucocorticoid receptor. Compared with the angiotensin II type 1A receptor promoter, no effect by dexamethasone was observed in vascular smooth muscle cells transfected with the angiotensin II type 1B receptor promoter/luciferase reporter gene constructs. We concluded that the dexamethasone-induced increase in the transcription of the angiotensin II type 1A receptor gene occurred through the binding to GRE up the glucocorticoid-specific receptor.
机译:糖皮质激素刺激大鼠血管紧张素II 1A型受体基因的转录。为了阐明在大鼠血管平滑肌细胞中糖皮质激素作用的分子机制,我们通过使用启动子/荧光素酶报告基因基因构建体和异源环境构建体(包含胸苷激酶启动子)研究了地塞米松对血管紧张素II型1A受体启动子活性的影响。 )转染的血管平滑肌细胞中。启动子中存在三个假定的糖皮质激素响应元件。然而,仅发现一种糖皮质激素响应元件对地塞米松(1 microM)有响应。该区域位于转录起始位点上游-756至-770 bp的位置。糖皮质激素拮抗剂RU38486完全阻断了地塞米松的诱导作用,表明糖皮质激素反应元件通过特定的糖皮质激素受体起作用。与血管紧张素II 1A型受体启动子相比,在用血管紧张素II 1B型受体启动子/荧光素酶报告基因构建体转染的血管平滑肌细胞中未观察到地塞米松的作用。我们得出的结论是,地塞米松诱导的血管紧张素II型1A受体基因转录的增加是通过与GRE结合糖皮质激素特异性受体而发生的。

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