Takeda K, Tanaka T, Shi W, Matsumoto M, Minami M, Kashiwamura S, Nakanishi K, Yoshida N, Kishimoto T, Akira S
Institute for Molecular and Cellular Biology, Osaka University, Japan.
Nature. 1996 Apr 18;380(6575):627-30. doi: 10.1038/380627a0.
Interleukin-4 (IL-4) is a pleiotropic lymphokine which plays an important role in the immune system. IL-4 activates two distinct signalling pathways through tyrosine phosphorylation of Stat6, a signal transducer and activator of transcription, and of a 170K protein called 4PS. To investigate the functional role of Stat6 in IL-4 signalling, we generated mice deficient in Stat6 by gene targeting. We report here that in the mutant mice, expression of CD23 and major histocompatibility complex (MHC) class II in resting B cells was not enhanced in response to IL-4. IL-4 induced B-cell proliferation costimulated by anti-IgM antibody was abolished. The T-cell proliferative response was also notably reduced. Furthermore, production of Th2 cytokines from T cells as well as IgE and IgG1 responses after nematode infection were profoundly reduced. These findings agreed with those obtained in IL-4 deficient mice or using antibodies to IL-4 and the IL-4 receptor. We conclude that Stat6 plays a central role in exerting IL-4 mediated biological responses.
白细胞介素-4(IL-4)是一种多效性淋巴因子,在免疫系统中发挥重要作用。IL-4通过信号转导及转录激活因子Stat6和一种名为4PS的170K蛋白的酪氨酸磷酸化激活两条不同的信号通路。为研究Stat6在IL-4信号传导中的功能作用,我们通过基因打靶产生了Stat6缺陷型小鼠。我们在此报告,在突变小鼠中,静息B细胞中CD23和主要组织相容性复合体(MHC)II类分子的表达不会因IL-4而增强。IL-4诱导的由抗IgM抗体共刺激的B细胞增殖被消除。T细胞增殖反应也显著降低。此外,线虫感染后T细胞产生的Th2细胞因子以及IgE和IgG1反应也大幅减少。这些发现与在IL-4缺陷型小鼠中或使用抗IL-4和IL-4受体抗体所获得的结果一致。我们得出结论,Stat6在发挥IL-4介导的生物学反应中起核心作用。