Jacobson N G, Szabo S J, Weber-Nordt R M, Zhong Z, Schreiber R D, Darnell J E, Murphy K M
Department of Pathology, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
J Exp Med. 1995 May 1;181(5):1755-62. doi: 10.1084/jem.181.5.1755.
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.
白细胞介素12(IL - 12)启动初始CD4 + T细胞向1型辅助性T细胞(Th1)分化,这对于抵抗细胞内病原体如硕大利什曼原虫至关重要。为了探究IL - 12作用的基础,我们分析了Th1细胞中核因子的诱导情况。IL - 12选择性地诱导了包含Stat3和Stat4的核DNA结合复合物,Stat3和Stat4是信号转导子和转录激活子(STATs)家族最近克隆的成员。虽然Stat3参与其他几种细胞因子的信号传导,但此前并不知道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的配体激活情况。