IL-10 down-regulates human microglial IL-8 by inhibition of NF-κB activation

被引:41
|
作者
Ehrlich, LC
Hu, SX
Peterson, PK
Chao, CC
机构
[1] Minneapolis Med Res Fdn, Inst Brain & Immune Disorders, Minneapolis, MN 55404 USA
[2] Univ Minnesota, Sch Med, Minneapolis, MN 55404 USA
关键词
IL-8; IL-10; inflammation; microglia; transcription factors;
D O I
10.1097/00001756-199806010-00010
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
IN the present study, we tested the hypothesis that interleukin (IL)-10 down-regulates human microglial cell IL-8 release by inhibiting activation of nuclear factor kappa B (NF-kappa B). Immunohistochemical staining demonstrated that IL-10 markedly suppressed lipopolysaccharide (LPS)- and IL-1 beta-stimulated IL-8 expression. NF-kappa B involvement was suggested by the finding that pyrrolidinedithiocarbamate, a known inhibitor elf NF-kappa B activation, blocked LPS- and IL-1 beta-induced IL-8 production. Consistent with our hypothesis, IL-10 treatment of LPS- and IL-1 beta-stimulated microglia was associated with a marked decrease in NF-kappa B translocation from the cytoplasm to the nucleus. (C) 1998 Rapid Science Ltd.
引用
收藏
页码:1723 / 1726
页数:4
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