Role of ephrin B2 in human retinal endothelial cell proliferation and migration

被引:63
|
作者
Steinle, JJ
Meininger, CJ
Chowdhury, U
Wu, GY
Granger, HJ
机构
[1] Texas A&M Univ, Coll Med, Syst Hlth Sci Ctr, Cardiovasc Res Inst, Temple, TX 76504 USA
[2] Texas A&M Univ, Coll Med, Syst Hlth Sci Ctr, Dept Med Physiol, Temple, TX 76504 USA
[3] Texas A&M Univ, Dept Anim Sci, College Stn, TX 77843 USA
关键词
retina; endothelial cell; angiogenesis; matrix metalloproteinase; eye; blood vessel;
D O I
10.1016/S0898-6568(03)00072-X
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
This study was designed to determine the presence of Eph B4 or ephrin B2 in human retinal endothelial cells (REC) and their signal transduction. Human retinal endothelial cells were stimulated with an Eph B4/Fc chimera and probed for phosphorylation of phosphatidylinositol-3-kinase (PI3K), Sre, and mitogen-activated protein kinase (MAPK) pathways. Proliferation and migration were investigated after Eph B4/Fc stimulation in the presence of various pathway inhibitors. Human retinal endothelial cells express ephrin B2, with little expression of Eph B4. Treatment with EphB4/Fc chimera resulted in activation of PI3K, Src, and MAPK pathways. Eph B4-stimulated endothelial cell proliferation was mediated via PI3K, nitric oxide synthase, and extracellular signal-regulated kinase 1/2 (ERK1/2). Blockade of Src-PI3K pathways produced significant attenuation of Eph B4/Fc-stimulated migration. These results demonstrate for the first time that ephrin B2 is present in human retinal endothelial cells. Additionally, it appears that vascular growth may be modulated in the retina through activation of the PI3K pathway and its downstream components. (C) 2003 Elsevier Science Inc, All rights reserved.
引用
收藏
页码:1011 / 1017
页数:7
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