Synergistic stimulation, by tumor necrosis factor-α and interferon-γ, of fractalkine expression in human astrocytes

被引:78
|
作者
Yoshida, H
Imaizumi, T
Fujimoto, K
Matsuo, N
Kimura, K
Cui, XF
Matsumiya, T
Tanji, K
Shibata, T
Tamo, W
Kumagai, M
Satoh, K
机构
[1] Hirosaki Univ, Sch Med, Inst Brain Sci, Dept Vasc Biol, Hirosaki, Aomori 0368562, Japan
[2] Hirosaki Univ, Sch Med, Dept Dent & Oral Surg, Hirosaki, Aomori 0368562, Japan
[3] Hirosaki Univ, Sch Med, Inst Brain Sci, Dept Mol Biol, Hirosaki, Aomori 0368562, Japan
关键词
fractalkine; CX3C; neurotactin; cytokines; astroglia; reverse transcription-polymerase chain reaction; enzyme-linked immunosorbent assay;
D O I
10.1016/S0304-3940(01)01699-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Fractalkine is a CX3C chemonkine that appears to be a neuron-to-microglia signal molecule in the central nervous system. We studied the expression of fractalkine in normal human astrocytes in culture, by using semi-quantitative reverse transcription-polymerase chain reaction and enzyme-linked immunosorbent assay. We found that tumor-necrosis factor alpha (TNF-alpha) and interferon-gamma (IFN-gamma) synergistically enhance the expression of fractalkine. The expression of both fractalkine mRNA and protein was increased in time- and concentration-dependent manners in the cells co-stimulated with TNF-alpha and IFN-gamma. Cycloheximide, an inhibitor of protein synthesis, and dexamethasone had no effect on the synergy of the stimulation of fractalkine expression. We conclude that normal human astrocytes produce fractalkine by costimulation with pro-inflammatory cytokines and it may serve as a potential signal for immune and inflammatory responses in the central nervous system. (C) 2001 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:132 / 136
页数:5
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