Keegan A D, Johnston J A, Tortolani P J, McReynolds L J, Kinzer C, O'Shea J J, Paul W E
Laboratory of Immunology, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Proc Natl Acad Sci U S A. 1995 Aug 15;92(17):7681-5. doi: 10.1073/pnas.92.17.7681.
The cytokines interleukin (IL) 4 and IL-13 induce many of the same biological responses, including class switching to IgE and induction of major histocompatibility complex class II antigens and CD23 on human B cells. It has recently been shown that IL-4 induces the tyrosine phosphorylation of a 170-kDa protein, a substrate called 4PS, and of the Janus kinase (JAK) family members JAK1 and JAK3. Because IL-13 has many functional effects similar to those of IL-4, we compared the ability of IL-4 and IL-13 to activate these signaling molecules in the human multifactor-dependent cell line TF-1. In this report we demonstrate that both IL-4 and IL-13 induced the tyrosine phosphorylation of 4PS and JAK1. Interestingly, although IL-4 induced the tyrosine phosphorylation of JAK3, we did not detect JAK3 phosphorylation in response to IL-13. These data suggest that IL-4 and IL-13 signal in similar ways via the activation of JAK1 and 4PS. However, our data further indicate that there are significant differences because IL-13 does not activate JAK3.
细胞因子白细胞介素(IL)-4和IL-13可诱导许多相同的生物学反应,包括向IgE的类别转换以及诱导人B细胞上的主要组织相容性复合体II类抗原和CD23。最近有研究表明,IL-4可诱导一种170 kDa蛋白(称为4PS的底物)以及Janus激酶(JAK)家族成员JAK1和JAK3的酪氨酸磷酸化。由于IL-13具有许多与IL-4相似的功能效应,我们比较了IL-4和IL-13在人多因子依赖性细胞系TF-1中激活这些信号分子的能力。在本报告中,我们证明IL-4和IL-13均可诱导4PS和JAK1的酪氨酸磷酸化。有趣的是,尽管IL-4可诱导JAK3的酪氨酸磷酸化,但我们未检测到IL-13诱导的JAK3磷酸化。这些数据表明,IL-4和IL-13通过激活JAK1和4PS以相似的方式发出信号。然而,我们的数据进一步表明存在显著差异,因为IL-13不会激活JAK3。