Neurotrophins and the anti-inflammatory agents interleukin-4 (IL-4), IL-10, IL-11 and transforming growth factor-β1 (TGF-β1) down-regulate T cell costimulatory molecules B7 and CD40 on cultured rat microglia

被引:101
作者
Wei, RT [1 ]
Jonakait, GM [1 ]
机构
[1] Rutgers State Univ, Dept Biol Sci, Newark, NJ 07102 USA
关键词
B7-1; B7-2; CD40; costimulation; GM-CSF; interferon-gamma; TGF-beta; 1; NGF;
D O I
10.1016/S0165-5728(98)00248-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Microglia are essential for T cell activation in the CNS. Since T cell activation requires costimulation by B7 and/or CD40, we examined the regulation by cytokines of B7-1, B7-2 and CD40 mRNA expression in cultured rat microglia in serum-foe medium. All three ligands are expressed constitutively, but are profoundly up-regulated by granulocyte-macrophage colony-stimulating factor (GEL I-CSF). By contrast, interferon-gamma raises only B7-2 and CD30 mRNA, and the B7-2 increase is inhibited by IL-10. IL-4, transforming growth factor-beta 1, and nerve growth factor (NGF) repress GM-CSF-induced B7-2 and CD40, but not B7-1. NGF also down-regulates its own high-affinity trkA receptor. IL-11, unrecognized for its effect on antigen presentation, represses GM-CSF-induced B7-2. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:8 / 18
页数:11
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