Interferon-γ stimulates the expression of CX3CL1/fractalkine in cultured human endothelial cells

被引:52
作者
Imaizumi, T
Matsumiya, T
Fujimoto, K
Okamoto, K
Cui, XF
Ohtaki, U
Yoshida, H
Satoh, K
机构
[1] Hirosaki Univ, Sch Med, Inst Brain Sci, Dept Vasc Surg, Hirosaki, Aomori 0368562, Japan
[2] Hirosaki Univ, Sch Med, Dept Dent & Oral Surg, Hirosaki, Aomori 0368562, Japan
关键词
fractalkine; endothelial cells; interferon-gamma;
D O I
10.1620/tjem.192.127
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
CX3CL1/Fractalkine, a CX3C chemokine, is a potent agonist for the chemotaxis and adhesion of monocytes and lymphocytes. It was first identified as a membrane protein in endothelial cells activated with IL-1 or TNF-alpha. We have found the enhanced expression of fractalkine in human umbilical vein endothelial cells stimulated with interferon-gamma (IFN-gamma). Pretreatment of the cells with cycloheximide did not inhibit the expression of fractalkine mRNA. The majority of fractalkine protein was found in the cell lysate, and an antibody-blocking experiment disclosed that fractalkine contributes to the adhesion of mononuclear cells to endothelial monolayers stimulated with IFN-gamma. Vascular endothelial cells produce fractalkine in response to IFN-gamma, and this may play an important role in immune responses by eliciting a traffic of mononuclear cells through the vascular wall. (C) 2000 Tohoku University Medical Press.
引用
收藏
页码:127 / 139
页数:13
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