Early growth response-1 in cardiovascular pathobiology

被引:254
作者
Khachigian, LM [1 ]
机构
[1] Univ New S Wales, Dept Pathol, Ctr Vasc Res, Sydney, NSW 2052, Australia
[2] Prince Wales Hosp, Dept Haematol, Sydney, NSW, Australia
关键词
Egr-1; atherosclerosis; vascular injury; angiogenesis; ischemia and ischemia-reperfusion; allograft rejection; cardiac hypertrophy;
D O I
10.1161/01.RES.0000200177.53882.c3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The immediate-early gene product and zinc finger transcription factor early growth response (Egr)-1 plays a key master regulatory role in multiple cardiovascular pathological processes. This article reviews the amassing recent evidence implicating Egr-1 in atherosclerosis, intimal thickening after acute vascular injury, ischemic pathology, angiogenesis, allograft rejection, and cardiac hypertrophy.
引用
收藏
页码:186 / 191
页数:6
相关论文
共 86 条
[11]   Inhibition of the RelA(p65) NF-κB subunit by Egr-1 [J].
Chapman, NR ;
Perkins, ND .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (07) :4719-4725
[12]   Involvement of Egr-1/RelA synergy in distinguishing T cell activation from tumor necrosis factor-alpha-induced NF-kappa B1 transcription [J].
Cogswell, PC ;
Mayo, MW ;
Baldwin, AS .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 185 (03) :491-497
[13]   Angiotensin II (ATII)-inducible platelet-derived growth factor A-chain gene expression is p42/44 extracellular signal-regulated kinase-1/2 and Egr-1-dependent and mediated via the ATII type 1 but not type 2 receptor - Induction by ATII antagonized by nitric oxide [J].
Day, FL ;
Rafty, LA ;
Chesterman, CN ;
Khachigian, LM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (34) :23726-23733
[14]   Early growth response proteins (EGR) and nuclear factors of activated T cells (NFAT) form heterodimers and regulate proinflammatory cytokine gene expression [J].
Decker, EL ;
Nehmann, N ;
Kampen, E ;
Eibel, H ;
Zipfel, PF ;
Skerka, C .
NUCLEIC ACIDS RESEARCH, 2003, 31 (03) :911-921
[15]   The early growth response protein (EGR-1) regulates interleukin-2 transcription by synergistic interaction with the nuclear factor of activated T cells [J].
Decker, EL ;
Skerka, C ;
Zipfel, PF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (41) :26923-26930
[16]   FGF-1-induced platelet-derived growth factor-A chain gene expression in endothelial cells involves transcriptional activation by early growth response factor-1 [J].
Delbridge, GJ ;
Khachigian, LM .
CIRCULATION RESEARCH, 1997, 81 (02) :282-288
[17]   Elevated Egr-1 in human atherosclerotic cells transcriptionally represses the transforming growth factor-β type II receptor [J].
Du, BH ;
Fu, CZ ;
Kent, KC ;
Bush, H ;
Schulick, AH ;
Kreiger, K ;
Collins, T ;
McCaffrey, TA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (50) :39039-39047
[18]   Locked nucleic acid modified DNA enzymes targeting early growth response-1 inhibit human vascular smooth muscle cell growth [J].
Fahmy, RG ;
Khachigian, LM .
NUCLEIC ACIDS RESEARCH, 2004, 32 (07) :2281-2285
[19]   Transcription factor Egr-1 supports FGF-dependent angiogenesis during neovascularization and tumor growth [J].
Fahmy, RG ;
Dass, CR ;
Sun, LQ ;
Chesterman, CN ;
Khachigian, LM .
NATURE MEDICINE, 2003, 9 (08) :1026-1032
[20]   Egr-1 target genes in human endothelial cells identified by microarray analysis [J].
Fu, MG ;
Zhu, XJ ;
Zhang, JF ;
Liang, J ;
Lin, YM ;
Zhao, LN ;
Ehrengruber, MU ;
Chen, YQE .
GENE, 2003, 315 :33-41