Japanese encephalitis virus up-regulates expression of macrophage migration inhibitory factor (MTF) mRNA in the mouse brain

被引:31
作者
Suzuki, T
Ogata, A
Tashiro, K
Nagashima, K
Tamura, M
Yasui, K
Nishihira, J [1 ]
机构
[1] Hokkaido Univ, Sch Med, Cent Res Inst, Sapporo, Hokkaido 060, Japan
[2] Hokkaido Univ, Sch Med, Dept Neurol, Sapporo, Hokkaido 060, Japan
[3] Hokkaido Univ, Sch Med, Dept Pathol, Sapporo, Hokkaido 060, Japan
[4] Hokkaido Univ, Div Biophys, Res Inst Elect Sci, Sapporo, Hokkaido 060, Japan
[5] Tokyo Metropolitan Inst Neurosci, Dept Microbiol & Immunol, Tokyo, Japan
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENE STRUCTURE AND EXPRESSION | 2000年 / 1517卷 / 01期
关键词
cytokine; Japanese encephalitis virus; macrophage migration inhibitory factor; neuron; tumor necrosis factor-alpha;
D O I
10.1016/S0167-4781(00)00262-1
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
Macrophage migration inhibitory factor (MIF) is known as a proinflammatory cytokine, glucocorticoid-induced immunomodulator, and pituitary hormone, and contributes to broad-spectrum immune and inflammatory response. To investigate the expression of MIF in the central nervous system in an event of viral infection, we evaluated MIF mRNA expression in the mouse brain infected with Japanese encephalitis virus (JEV). In situ hybridization revealed that MIF mRNA expression was significantly up-regulated in the whole brain by intracranial JEV inoculation at 2 days post-inoculation (d.p.i.). Neurons as well as glial cells expressed MIF transcripts in which some of these cells were co-labeled by double staining for JEV antigens and MIF mRNA. At 4 d.p.i., when typical symptoms of encephalitis were observed, JEV antigen-positive cells were much increased in parallel with enhanced MIF mRNA, consistent with the results of Northern blot analysis. Reverse transcription-polymerase chain reaction showed that MIF mRNA was minimally changed at 1 d.p.i, in comparison with that at 0 d.p.i., but markedly up-regulated after 2 d.p.i. and sustained up to 4 d.p.i, On the other hand, a significant increase of tumor necrosis factor (TNF)-alpha mRNA was observed after only 3 d.p.i. These data suggest the possibility that MIF is involved in virus-induced encephalitis with regard to not only immune responses in the early stage, but also the exacerbation of inflammation in concert with TNF-alpha in the late stages. This is the first evidence demonstrating that MIF is up-regulated in the case of virus-induced encephalitis, which should contribute to the further understanding of the pathological mechanism of JEV-induced encephalitis. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:100 / 106
页数:7
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