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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >Inducible Expression of Stat4 in Dendritic Cells and Macrophages and Its Critical Role in Innate and Adaptive Immune Responses
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Inducible Expression of Stat4 in Dendritic Cells and Macrophages and Its Critical Role in Innate and Adaptive Immune Responses

机译:Stat4在树突状细胞和巨噬细胞中的诱导表达及其在先天和适应性免疫应答中的关键作用

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Autocrine activation of A PC by IL-12 has recently been revealed; we demonstrate here that inducible expression of Stat4 in A PC is central to this process. Stat4 is induced in dendritic cells (DC) in a maturation-dependent manner and in macrophages in an activation-dependent manner. Stat4 levels directly correlate with IL-12-dependent IFN-y production by A PC as well as IFN-y production by DC during Ag presentation. The Th2 cytokines IL-4 and IL-10 suppress Stat4 induction in DC and macrophages when present during maturation and activation, respectively, diminishing IFN-y production. In contrast, IL-4 has no effect on Stat4 levels in mature DC and actually augments IFN-y production by DC during Ag presentation, indicating that IL-4 acts differently in a spatiotemporal manner. The functional importance of Stat4 is evident in Stat4 -1- DC and macrophages, which fail to produce IFN-y. Furthermore, Stat4-1- macrophages are defective in NO production in response to IL-12 and are susceptible to Toxoplasma. Autocrine IL-12 signaling is required for high-Ievel IFN-y production by A PC at critical stages in both innate and adaptive immunity, and the control of Stat4 expression is likely an important regulator of this process.
机译:最近发现IL-12能自分泌激活A PC。我们在这里证明了Stat4在PC中的可诱导表达是该过程的关键。 Stat4在树突状细胞(DC)中以成熟依赖方式被诱导,在巨噬细胞中以活化依赖方式被诱导。 Stat4水平与Ag提呈过程中APC产生的IL-12依赖性IFN-y以及DC产生的IFN-y直接相关。当在成熟和激活过程中存在时,Th2细胞因子IL-4和IL-10分别抑制DC和巨噬细胞中的Stat4诱导,从而减少IFN-γ的产生。相反,IL-4对成熟DC中的Stat4水平没有影响,并且实际上在Ag呈递过程中通过DC增强了IFN-γ的产生,表明IL-4的时空行为有所不同。 Stat4的功能重要性在Stat4 -1- DC和巨噬细胞中很明显,它们无法产生IFN-γ。此外,Stat4-1-巨噬细胞在响应IL-12的NO产生中有缺陷,并且对弓形虫敏感。 APC在先天免疫和适应性免疫的关键阶段,高分泌IFN-γ均需要自分泌IL-12信号传导,而Stat4表达的控制可能是该过程的重要调节剂。

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