首页> 美国卫生研究院文献>The Journal of Experimental Medicine >Interleukin 12 signaling in T helper type 1 (Th1) cells involves tyrosine phosphorylation of signal transducer and activator of transcription (Stat)3 and Stat4
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Interleukin 12 signaling in T helper type 1 (Th1) cells involves tyrosine phosphorylation of signal transducer and activator of transcription (Stat)3 and Stat4

机译:T辅助1型(Th1)细胞中的白介素12信号传导涉及信号转导子和转录激活子(Stat)3和Stat4的酪氨酸磷酸化

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摘要

Interleukin 12 (IL-12) initiates the differentiation of naive CD4+ T cells to T helper type 1 (Th1) cells critical for resistance to intracellular pathogens such as Leishmania major. To explore the basis of IL-12 action, we analyzed induction of nuclear factors in Th1 cells. IL-12 selectively induced nuclear DNA-binding complexes that contained Stat3 and Stat4, recently cloned members of the family of signal transducers and activators of transcription (STATs). While Stat3 participates in signaling for several other cytokines, Stat4 was not previously known to participate in the signaling pathway for any natural ligand. The selective activation of Stat4 provides a basis for unique actions of IL-12 on Th1 development. Thus, this study presents the first identification of the early events in IL-12 signaling in T cells and of ligand activation of Stat4.
机译:白细胞介素12(IL-12)引发幼稚CD4 + T细胞分化为T辅助1型(Th1)细胞,这些细胞对抵抗细胞内病原体(如利什曼原虫)至关重要。为了探索IL-12作用的基础,我们分析了Th1细胞中核因子的诱导。 IL-12选择性诱导包含Stat3和Stat4的核DNA结合复合物,它们是最近克隆的信号转导子和转录激活子(STATs)家族的成员。尽管Stat3参与其他几种细胞因子的信号传导,但以前未知Stat4参与任何天然配体的信号传导途径。 Stat4的选择性激活为IL-12对Th1发育的独特作用提供了基础。因此,本研究首次鉴定了T细胞中IL-12信号传导的早期事件以及Stat4的配体活化。

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