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T细胞命运与功能:蛋白激酶C-θ及其他

T-cell fate and function: PKC-theta and beyond.

作者信息

Marsland Benjamin J, Kopf Manfred

机构信息

Institute of Integrative Biology, Molecular Biomedicine, Swiss Federal Institute of Technology ETH, CH-8952 Zurich, Switzerland.

出版信息

Trends Immunol. 2008 Apr;29(4):179-85. doi: 10.1016/j.it.2008.01.005. Epub 2008 Mar 6.

Abstract

The serine/threonine-specific protein kinase C-theta (PKC-theta) is a core component of the immunological synapse that was shown in vitro to play a central role in the activation of T cells after T cell receptor (TCR) and co-stimulatory molecule engagement. In recent years, a series of in vivo studies have shown that the situation is far more complex; specifically, PKC-theta signaling is differentially required for Th1, Th2, Th17 and CD8+ cytotoxic T-cell responses. These studies highlight the combination of signals that directly regulate T-cell differentiation and effector responses. In this review, we highlight recent in vivo studies investigating PKC-theta function and discuss this in the context of how the integration of extrinsic signals determines T cell fate and function.

摘要

丝氨酸/苏氨酸特异性蛋白激酶C-θ(PKC-θ)是免疫突触的核心组成部分,体外研究表明,在T细胞受体(TCR)和共刺激分子结合后,PKC-θ在T细胞激活中起核心作用。近年来,一系列体内研究表明情况要复杂得多;具体而言,Th1、Th2、Th17和CD8+细胞毒性T细胞反应对PKC-θ信号的需求各不相同。这些研究突出了直接调节T细胞分化和效应反应的信号组合。在本综述中,我们重点介绍了最近研究PKC-θ功能的体内研究,并在外部信号整合如何决定T细胞命运和功能的背景下进行了讨论。

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