Hayashi Keitaro, Altman Amnon
Division of Cell Biology, La Jolla Institute for Allergy and Immunology, 9420 Athena Circle, La Jolla, CA 92037, USA.
Pharmacol Res. 2007 Jun;55(6):537-44. doi: 10.1016/j.phrs.2007.04.009. Epub 2007 May 1.
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.
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。