趋化因子
效应器
细胞因子
SOCS3
生物
细胞生物学
炎症
受体
基因
内生
信号转导
基因表达
车站3
免疫学
分子生物学
内分泌学
生物化学
作者
Roland Lang,Divyen H. Patel,John J. Morris,Robert Rutschman,Peter J. Murray
出处
期刊:Journal of Immunology
[American Association of Immunologists]
日期:2002-09-01
卷期号:169 (5): 2253-2263
被引量:612
标识
DOI:10.4049/jimmunol.169.5.2253
摘要
IL-10 regulates inflammation by reducing cytokine and chemokine production from activated macrophages. We performed microarray experiments to identify possible effector molecules of IL-10 and to investigate the global effect of IL-10 on the transcriptional response induced in LPS-activated macrophages. To exclude background effects of endogenous IL-10, macrophages from IL-10-deficient mice were used. IL-10 up-regulated expression of a small number of genes (26 and 37 after 45 min and 3 h, respectively), including newly identified and previously documented targets such as suppressor of cytokine signaling-3 and IL-1 receptor antagonist. However, the activation program triggered by LPS was profoundly affected by IL-10. IL-10 repressed 62 and further increased 15 of 259 LPS-induced genes. For all genes examined, the effects of IL-10 were determined to be STAT3-dependent. These results suggest that IL-10 regulates STAT3-dependent pathways that selectively target a broad component of LPS-induced genes at the mRNA level.
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