Egr-1 target genes in human endothelial cells identified by microarray analysis

被引:135
作者
Fu, MG
Zhu, XJ
Zhang, JF
Liang, J
Lin, YM
Zhao, LN
Ehrengruber, MU
Chen, YQE
机构
[1] Morehouse Sch Med, Cardiovasc Res Inst, Dept Biochem, Atlanta, GA 30310 USA
[2] Peking Univ, Hlth Sci Ctr, Cardiovasc Res Inst, Beijing 100083, Peoples R China
[3] Univ Zurich, Brain Res Inst, CH-8057 Zurich, Switzerland
关键词
transcription; functional genomics; gene expression; vascular injury;
D O I
10.1016/S0378-1119(03)00730-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Early growth response factor 1 (Egr-1) is a key transcriptional factor to mediate gene expression after vascular injury. To better understand the role of Egr-1 in vasculature, we globally profiled Egr-1 target genes in human endothelial cells using adenoviral gene transfer and Affymetrix oligonucleotide-based microarray technology. More than 300 genes regulated by greater than or equal to 3-fold with Egr-1 overexpression were identified and, partially, confirmed by Northern and Western blotting, including genes for transcriptional regulators, signaling proteins, cell cycle regulatory proteins, growth factors, and cytokines. Among them, thymus-expressed chemokine (TECK) and IP-30 were dramatically induced by Egr-1, but TNFalpha-related apoptosis inducing ligand (TRAIL) was significantly repressed by Egr-1, suggesting that Egr-1 is a key mediator of inflammation and apoptosis in vascular cells. These data provide novel Egr-1 target genes and contribute to the understanding of the role of Egr-1 in vasculature. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:33 / 41
页数:9
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