共 4 条
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.
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页码:78 / 88
页数:11
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