Transcriptome analysis of aldosterone-regulated genes in human vascular endothelial cell lines stably expressing mineralocorticoid receptor

被引:22
作者
Sekizawa, Naoko [1 ]
Yoshimoto, Takanobu [1 ]
Hayakawa, Eri [1 ]
Suzuki, Noriko [1 ]
Sugiyama, Toru [1 ]
Hirata, Yukio [1 ]
机构
[1] Tokyo Med & Dent Univ, Dept Clin & Mol Endocrinol, Grad Sch, Bunkyo Ku, Tokyo 1138513, Japan
关键词
Aldosterone; Mineralocorticoid receptor; Endothelial cell; Gene expression; CARDIOVASCULAR-SYSTEM; IN-VITRO; ANGIOGENESIS; HYPERTENSION; GENERATION; INCREASES; ADHESION; HORMONE; NETWORK; PATHWAY;
D O I
10.1016/j.mce.2011.05.029
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A series of studies have demonstrated that endothelial cell is one of the target tissues of aldosterone. Here, we have conducted a transcriptome analysis of aldosterone-inducible genes in human endothelial cell lines stably expressing human mineralocorticoid receptor (MR) by retroviral system (MR-EAhy). We found that aldosterone in physiologic concentrations robustly induced MR-dependent transcriptional response in MR-EAhy. By DNA microarray analysis, we validated 12 aldosterone-up-regulated genes among which at least seven were concomitantly associated with increased protein expression. We also found five aldosterone-down-regulated genes. Among 11 aldosterone-up-regulated genes tested, mRNA expressions of three (ESM1, SNF1LK, ANGPTL4) were significantly up-regulated in aortic tissue from aldosterone-induced hypertensive rats compared to those from control rats, suggesting their potential pathophysiologic significance in vivo. In conclusion, using MR stably expressed human endothelial cell lines, we identified a variety of aldosterone-inducible genes, suggesting their possible roles in the development and/or the protection for aldosterone-induced vascular injury. (C) 2011 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:78 / 88
页数:11
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