Kinetics of IL-10-induced gene expression in human macrophages

被引:22
作者
Antoniv, TT [1 ]
Park-Min, KH [1 ]
Ivashkiv, LB [1 ]
机构
[1] Cornell Univ, Weill Grad Sch Med Sci, Grad Program Immunol, New York, NY 10021 USA
基金
美国国家卫生研究院;
关键词
expression profiling; interleukin-10; macrophages; prostaglandin dehydrogenase;
D O I
10.1016/j.imbio.2005.05.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IL-10 is a strong inhibitor of macrophage (M Phi) activation and inflammatory cytokine and chemokine production. To gain insight into mechanisms by which IL-10 suppresses inflammation, we performed a kinetic analysis of IL-10-induced gene expression in primary human M(D. IL-10 induced rapid and transient expression of genes encoding transcription factors, followed by sustained elevation or suppression of gene expression. IL-10 suppressed basal expression of interferon-inducible genes, suggesting that IL-10 interrupts autocrine interferon-mediated priming. IL-10 induced the expression of prostaglandin dehydrogenase (PGDH), the major catabolic enzyme involved in prostaglandin degradation. Concomitant with PGDH expression, IL-10 'induced increased degradation of the inflammatory PGE(2) and suppressed PGE(2)-mediated effects on M Phi morphology and gene expression. These results identify catabolism of inflammatory PGs as a mechanism of IL-10 anti-inflammatory action. (C) 2005 Elsevier GmbH. All rights reserved.
引用
收藏
页码:87 / 95
页数:9
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