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蛋白激酶C(θ)在T细胞活化中的作用

Protein kinase C(theta) in T cell activation.

作者信息

Isakov Noah, Altman Amnon

机构信息

Department of Microbiology and Immunology, Faculty of Health Sciences, and the Cancer Research Center, Ben Gurion University of the Negev, Beer Sheva 84105, Israel.

出版信息

Annu Rev Immunol. 2002;20:761-94. doi: 10.1146/annurev.immunol.20.100301.064807.

Abstract

The novel protein kinase C (PKC) isoform, PKC theta, is selectively expressed in T lymphocytes and is a sine qua non for T cell antigen receptor (TCR)-triggered activation of mature T cells. Productive engagement of T cells by antigen-presenting cells (APCs) results in recruitment of PKC theta to the T cell-APC contact area--the immunological synapse--where it interacts with several signaling molecules to induce activation signals essential for productive T cell activation and IL-2 production. The transcription factors NF-kappa B and AP-1 are the primary physiological targets of PKC theta, and efficient activation of these transcription factors by PKC theta requires integration of TCR and CD28 costimulatory signals. PKC theta cooperates with the protein Ser/Thr phosphatase, calcineurin, in transducing signals leading to activation of JNK, NFAT, and the IL-2 gene. PKC theta also promotes T cell cycle progression and regulates programmed T cell death. The exact mode of regulation and immediate downstream substrates of PKC theta are still largely unknown. Identification of these molecules and determination of their mode of operation with respect to the function of PKC theta will provide essential information on the mechanism of T cell activation. The selective expression of PKC theta in T cells and its essential role in mature T cell activation establish it as an attractive drug target for immunosuppression in transplantation and autoimmune diseases.

摘要

新型蛋白激酶C(PKC)同工型PKCθ在T淋巴细胞中选择性表达,是T细胞抗原受体(TCR)触发成熟T细胞活化所必需的。抗原呈递细胞(APC)与T细胞的有效结合导致PKCθ募集到T细胞-APC接触区域——免疫突触,在那里它与几种信号分子相互作用,以诱导对有效的T细胞活化和白细胞介素-2产生至关重要的活化信号。转录因子NF-κB和AP-1是PKCθ的主要生理靶点,PKCθ对这些转录因子的有效激活需要整合TCR和CD28共刺激信号。PKCθ与蛋白丝氨酸/苏氨酸磷酸酶钙调神经磷酸酶协同作用,转导导致JNK、NFAT和白细胞介素-2基因激活的信号。PKCθ还促进T细胞周期进程并调节程序性T细胞死亡。PKCθ的确切调节模式和直接下游底物在很大程度上仍然未知。鉴定这些分子并确定它们关于PKCθ功能的作用方式将提供有关T细胞活化机制的重要信息。PKCθ在T细胞中的选择性表达及其在成熟T细胞活化中的重要作用使其成为移植和自身免疫性疾病中免疫抑制的有吸引力的药物靶点。

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