Tebo J M, Kim H S, Gao J, Armstrong D A, Hamilton T A
Department of Immunology, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA.
Blood. 1998 Dec 15;92(12):4742-9.
Interleukin-10 (IL-10) selectively inhibited lipopolysaccharide (LPS)-induced chemoattractant cytokine gene expression: levels of IP-10 mRNA were markedly suppressed in IL-10-treated mouse peritoneal macrophages, whereas the expression of the RANTES mRNA was only modestly reduced. IL-10 inhibited IP-10 mRNA accumulation by reducing IP-10 gene transcription as demonstrated by nuclear run-on analysis. Interestingly, the ability of IL-10 to inhibit expression of IP-10 was dependent on the inducing stimulus; IL-10 did not suppress interferon gamma (IFNgamma)- or IFNbeta-stimulated IP-10 transcription or mRNA accumulation. These results suggested that IL-10 might act indirectly to suppress IP-10 expression by inhibiting LPS-induced class I IFN production. This hypothesis was supported by the following observations. First, LPS-induced IP-10 mRNA expression was blocked in cells cotreated with cycloheximide. Second, IL-10 inhibited the production of IFN/beta-mediated antiviral activity. Finally, the IL-10-mediated suppression of LPS-stimulated IP-10 production could be rescued by cotreatment with IFNbeta.
白细胞介素-10(IL-10)选择性抑制脂多糖(LPS)诱导的趋化因子细胞因子基因表达:在经IL-10处理的小鼠腹腔巨噬细胞中,IP-10 mRNA水平显著受到抑制,而RANTES mRNA的表达仅略有降低。如通过核转录分析所证实,IL-10通过减少IP-10基因转录来抑制IP-10 mRNA的积累。有趣的是,IL-10抑制IP-10表达的能力取决于诱导刺激;IL-10并不抑制干扰素γ(IFNγ)或干扰素β(IFNβ)刺激的IP-10转录或mRNA积累。这些结果表明,IL-10可能通过抑制LPS诱导的I类干扰素产生来间接抑制IP-10表达。以下观察结果支持了这一假设。首先,在用环己酰亚胺共同处理的细胞中,LPS诱导的IP-10 mRNA表达受到阻断。其次,IL-10抑制IFN/β介导的抗病毒活性的产生。最后,通过与IFNβ共同处理,可以挽救IL-10介导的对LPS刺激的IP-10产生的抑制作用。