Receptor tyrosine kinase Tie-1 overexpression in endothelial cells upregulates adhesion molecules

被引:27
作者
Chan, Barden [1 ,2 ]
Yuan, Hai-Tao [2 ]
Karumanchi, S. Ananth [2 ]
Sukhatme, Vikas P. [1 ]
机构
[1] Harvard Univ, Sch Med, Div Interdisciplinary Med & Biotechnol, Dept Med,Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Div Nephrol, Dept Med,Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
关键词
atherosclerosis; adhesion molecules; Tie-1;
D O I
10.1016/j.bbrc.2008.04.091
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tie-1 is an endothelial specific cell surface protein whose biology remains poorly understood. Using an overexpression system in vitro, we examined whether Tie-1 activity in endothelial cells in vitro would elicit a proinflammatory response. We found that when overexpressed in endothelial cells in vitro, Tie-1 is tyrosine-phosphorylated. We also showed that Tie-1 upregulates VCAM-1, E-selectin, and ICAM-1, partly through a p38-dependent mechanism. Interestingly, upregulation of VCAM-1 and E-selectin by Tie-1 is significantly higher in human aortic endothelial cells than in human umbilical vein endothelial cells. Additionally, attachment of cells of monocytic lineage to endothelial cells is also enhanced by Tie-1 expression. Collectively, our data show that Tie-1 has a proinflammatory property and may play a role in the endothelial inflammatory diseases such as atherosclerosis. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:475 / 479
页数:5
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