Theiler's virus infection induces the expression of cyclooxygenase-2 in murine astrocytes:: inhibition by the anti-inflammatory cytokines interleukin-4 and interleukin-10

被引:26
作者
Molina-Holgado, E
Arévalo-Martín, A
Ortiz, S
Vela, JM
Guaza, C
机构
[1] CSIC, Inst Cajal, Dept Plasticidad Neural, E-28002 Madrid, Spain
[2] Univ Autonoma Barcelona, Fac Med, Dept Biol Cellular Fisiol & Immunol, Unidat Histol, E-08193 Barcelona, Spain
关键词
Theiler's murine encephalomyelitis virus; prostaglandins; cycloxygenase-2; anti-inflammatory cytokines; murine astrocytes;
D O I
10.1016/S0304-3940(02)00209-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Theiler's murine encephalomyelitis virus (TMEV) causes an acute encephalomyelitis followed by a persistent infection of the central nervous system (CNS) resulting in a chronic inflammation and axonal demyelination in susceptible strains of mice. The pathogenesis of TMEV-induced demyelinating disease remains unknown, but infection of brain glial cells is a critical factor for virus persistence in the CNS. In the present study we investigated the effects of the anti-inflammatory cytokines interleukin-4 (IL-4) and interleukin-10 (IL-10) on the production of inflammatory mediators, such as prostaglandins, after infection of primary astroglial SJL/J murine cultures with TMEV. This infection resulted in a time-dependent transcription of the gene encoding cyclooxygenase-2 (COX-2) and an increased production of prostaglandin E2 (PGE(2)). Both, IL-4 but mainly, IL-10 (1 and 10 ng/ml) decreased the TMEV-induced expression of COX-2 as well as the synthesis of PGE(2). Interestingly, treatment with IL-10 completely abrogated COX-2 induction. The molecular mechanisms involved in the regulation of COX-2 expression by TMEV are unknown, but the effects of anti-inflammatory cytokines may involve the inhibition of the transcription factor nuclear factor B-K activity and lead to strategies capable of interrupting the inflammatory cascade triggered by TMEV in brain glial cells. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:237 / 241
页数:5
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