Following direct CD40 activation, human primary microglial cells produce IL-12 p40 but not bioactive IL-12 p70

被引:9
|
作者
de Herve, MGD
Delfraissy, JF
Taoufik, Y
机构
[1] Univ Paris 11, Lab Virus Neurone & Immun, Paris, France
[2] Univ Paris 11, Immunol Lab, Paris, France
[3] CHU Bicetre, Le Kremlin Bicetre, France
关键词
microglial cells; CD40; IL-12;
D O I
10.1006/cyto.2000.0855
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
There is accumulating evidence that interleukin 12 (IL-12) is involved in the pathogenesis of multiple sclerosis, In the periphery, this cytokine is produced by antigen-presenting cells (APCs) following interaction with activated T cells, CD40 ligation plays a crucial role in this production. Microglial cells are thought to play a major role in antigen presentation in the central nervous system. In this work, we examined IL-12 production by human primary microglial cells after CD40 ligation, These cells expressed CD40 and MHC class II following interferon-gamma activation. IL-12 p40 mRNA and protein, but not bioactive IL-12 p70, were detected in response to direct CD40 activation. Microglial cells co-cultured with activated allogenic CD4+ T lymphocytes also produced IL-12 p40 but not IL-12 p70, This IL-12 p40 production was inhibited by anti-CD40 ligand, Altogether, these results suggest that CD40-CD40-ligand interaction provides a signal that triggers IL-12 p40 expression. However, other interaction(s) may be required during antigen presentation for bioactive heterodimeric IL-12 p70 to be produced by microglial cells. (C) 2001 Academic Press.
引用
收藏
页码:88 / 96
页数:9
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