Suppr超能文献

由白细胞介素-2/白细胞介素-2受体β链相互作用介导的蛋白质磷酸化。

Protein phosphorylation mediated by IL-2/IL-2 receptor beta-chain interaction.

作者信息

Ishii T, Takeshita T, Numata N, Sugamura K

机构信息

Department of Bacteriology, Tohoku University School of Medicine, Sendai, Japan.

出版信息

J Immunol. 1988 Jul 1;141(1):174-9.

PMID:3132502
Abstract

We previously found that IL-2 rapidly induced protein phosphorylation of a 67-kDa (pp67) and four 63-kDa (pp63s) cellular proteins in various T cells. Here, we show that the IL-2-stimulated phosphorylation is mediated by the IL-2R beta-chain composed of the high affinity IL-2R, and induced by activation of Ca2+/phospholipid-dependent protein kinase C (PKC). The IL-2-stimulated phosphorylation was always observed in various T cell lines bearing high affinity IL-2R, but never observed in cells which express only low affinity IL-2R consisted of alpha-chain alone. When the expression of high affinity IL-2R was modified by anti-IL-2R mAb for reducing the affinity to 8- to 10-fold lower without affecting the sites of IL-2R, the effective dose of IL-2 on phosphorylation of pp67 increased 8 to 10 times. When cells were treated with pronase, approximately 95% sites of low affinity IL-2R were selectively decreased, but the IL-2 dose dependency for pp67 phosphorylation was little affected. These data exactly suggest that protein phosphorylation in response to IL-2 such as pp67 and pp63s, is mediated by high affinity but not low affinity IL-2R. Furthermore, the IL-2-stimulated phosphorylation of these proteins was also observed in MLA 144 cells which express only low affinity IL-2R consisting of beta-chain alone. In addition, various phorbol esters and tumor promoters, which activate PKC, were also demonstrated to induce the phosphorylation of a pp67 and pp63s in these T cell lines. Therefore, the present study suggests that IL-2/IL-2R beta-chain interaction triggers the phosphorylation of pp67 and pp63s, where the PKC may have an important role.

摘要

我们先前发现,白细胞介素-2(IL-2)可在多种T细胞中迅速诱导一种67 kDa(pp67)和四种63 kDa(pp63s)细胞蛋白的磷酸化。在此,我们表明,IL-2刺激的磷酸化是由高亲和力IL-2R的β链介导的,并由Ca2+/磷脂依赖性蛋白激酶C(PKC)的激活所诱导。在带有高亲和力IL-2R的多种T细胞系中总能观察到IL-2刺激的磷酸化,但在仅表达由α链单独组成的低亲和力IL-2R的细胞中从未观察到。当用抗IL-2R单克隆抗体修饰高亲和力IL-2R的表达,使其亲和力降低8至10倍而不影响IL-2R的位点时,IL-2对pp67磷酸化的有效剂量增加了8至10倍。当用链霉蛋白酶处理细胞时,低亲和力IL-2R约95%的位点被选择性减少,但IL-2对pp67磷酸化的剂量依赖性几乎未受影响。这些数据确切表明,对IL-2作出反应的蛋白磷酸化,如pp67和pp63s,是由高亲和力而非低亲和力IL-2R介导的。此外,在仅表达由β链单独组成的低亲和力IL-2R的MLA 144细胞中也观察到了这些蛋白的IL-2刺激的磷酸化。此外,各种激活PKC的佛波酯和肿瘤启动子也被证明可在这些T细胞系中诱导pp67和pp63s的磷酸化。因此,本研究表明,IL-2/IL-2Rβ链相互作用触发了pp67和pp63s的磷酸化,其中PKC可能起重要作用。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验