Fujii Hodaka
Department of Pathology, New York University School of Medicine, 550 First Avenue, MSB-126, New York, NY 10016, USA.
Biochem Biophys Res Commun. 2007 Mar 16;354(3):825-9. doi: 10.1016/j.bbrc.2007.01.067. Epub 2007 Jan 22.
Binding of interleukin-2 (IL-2) to its specific receptor induces activation of two members of Jak family protein tyrosine kinases, Jak1 and Jak3. An IL-2 receptor (IL-2R)-reconstituted NIH 3T3 fibroblast cell line proliferates in response to IL-2 only when hematopoietic lineage-specific Jak3 is ectopically expressed. However, the mechanism of Jak3-dependent proliferation in the fibroblast cell line is not known. Here, I showed that Jak3 expression is dispensable for IL-2-induced activation of Jak1 and Stat proteins and expression of nuclear proto-oncogenes in the IL-2R-reconstituted fibroblast cell line. Jak3 expression markedly enhanced these IL-2-induced signaling events. In contrast, Jak3 expression was essential for induction of cyclin genes involved in the G1-S transition. These data suggest a critical role of Jak3 in IL-2 signaling in the fibroblast cell line and may provide further insight into the cell type-specific mechanism of cytokine signaling.
白细胞介素-2(IL-2)与其特异性受体的结合可诱导Jak家族蛋白酪氨酸激酶的两个成员Jak1和Jak3的激活。只有当造血谱系特异性的Jak3异位表达时,IL-2受体(IL-2R)重构的NIH 3T3成纤维细胞系才会对IL-2产生增殖反应。然而,成纤维细胞系中Jak3依赖性增殖的机制尚不清楚。在此,我表明在IL-2R重构的成纤维细胞系中,Jak3的表达对于IL-2诱导的Jak1和Stat蛋白激活以及核原癌基因的表达并非必需。Jak3的表达显著增强了这些IL-2诱导的信号事件。相反,Jak3的表达对于诱导参与G1-S期转换的细胞周期蛋白基因至关重要。这些数据表明Jak3在成纤维细胞系的IL-2信号传导中起关键作用,并可能为细胞因子信号传导的细胞类型特异性机制提供进一步的见解。