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蛋白激酶Cθ(PKCθ):T细胞生死的关键参与者。

Protein kinase C theta (PKCtheta): a key player in T cell life and death.

作者信息

Hayashi Keitaro, Altman Amnon

机构信息

Division of Cell Biology, La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, La Jolla, CA 92037, USA.

出版信息

Pharmacol Res. 2007 Jun;55(6):537-44. doi: 10.1016/j.phrs.2007.04.009. Epub 2007 May 1.

Abstract

Protein kinase C theta (PKCtheta) is a member of the novel, Ca(2+)-independent PKC subfamily, which plays an important and non-redundant role in several aspects of T cell biology. Much progress has been accomplished in understanding the function of PKCtheta in the immune system and its unique translocation to the immunological synapse in Ag-stimulated T lymphocytes. Biochemical and genetic approaches revealed that PKCtheta is required for the activation of mature T cells as well as for their survival. Mutation of the PKCtheta gene leads to impaired receptor-induced stimulation of the transcription factors AP-1, NF-kappaB and NFAT, which results in defective T cell activation, and to aberrant expression of apoptosis-related proteins, resulting in poor T cell survival. Furthermore, PKCtheta-deficient mice display defects in the differentiation of T helper subsets, particularly in Th2- and Th17-mediated inflammatory responses. Therefore, PKCtheta is a critical enzyme that regulates T cell function at multiple stages, and it represents an attractive drug target for allergic and autoimmune diseases.

摘要

蛋白激酶Cθ(PKCθ)是新型的、不依赖钙离子的蛋白激酶C亚家族的成员,它在T细胞生物学的多个方面发挥着重要且不可替代的作用。在理解PKCθ在免疫系统中的功能以及其在抗原刺激的T淋巴细胞中独特地易位至免疫突触方面已经取得了很大进展。生化和遗传学方法表明,PKCθ对于成熟T细胞的激活及其存活是必需的。PKCθ基因的突变导致受体诱导的转录因子AP-1、NF-κB和NFAT的刺激受损,这导致T细胞激活缺陷,并导致凋亡相关蛋白的异常表达,从而导致T细胞存活率低下。此外,缺乏PKCθ的小鼠在辅助性T细胞亚群的分化方面存在缺陷,特别是在Th2和Th17介导的炎症反应中。因此,PKCθ是一种在多个阶段调节T细胞功能的关键酶,它是过敏性和自身免疫性疾病有吸引力的药物靶点。

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