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微管组织中心极性和免疫突触:蛋白激酶 C 及其他。

Microtubule-organizing center polarity and the immunological synapse: protein kinase C and beyond.

机构信息

Immunology Program, Memorial Sloan-Kettering Cancer Center , New York, NY, USA.

出版信息

Front Immunol. 2012 Jul 31;3:235. doi: 10.3389/fimmu.2012.00235. eCollection 2012.

Abstract

Cytoskeletal polarization is crucial for many aspects of immune function, ranging from neutrophil migration to the sampling of gut flora by intestinal dendritic cells. It also plays a key role during lymphocyte cell-cell interactions, the most conspicuous of which is perhaps the immunological synapse (IS) formed between a T cell and an antigen-presenting cell (APC). IS formation is associated with the reorientation of the T cell's microtubule-organizing center (MTOC) to a position just beneath the cell-cell interface. This cytoskeletal remodeling event aligns secretory organelles inside the T cell with the IS, enabling the directional release of cytokines and cytolytic factors toward the APC. MTOC polarization is therefore crucial for maintaining the specificity of a T cell's secretory and cytotoxic responses. It has been known for some time that T cell receptor (TCR) stimulation activates the MTOC polarization response. It has been difficult, however, to identify the machinery that couples early TCR signaling to cytoskeletal remodeling. Over the past few years, considerable progress has been made in this area. This review will present an overview of recent advances, touching on both the mechanisms that drive MTOC polarization and the effector responses that require it. Particular attention will be paid to both novel and atypical members of the protein kinase C family, which are now known to play important roles in both the establishment and the maintenance of the polarized state.

摘要

细胞骨架的极化对于免疫功能的许多方面都至关重要,从中性粒细胞的迁移到肠道树突状细胞对肠道菌群的采样。它在淋巴细胞细胞间相互作用中也起着关键作用,其中最明显的可能是 T 细胞和抗原呈递细胞 (APC) 之间形成的免疫突触 (IS)。IS 的形成与 T 细胞的微管组织中心 (MTOC) 重新定向到细胞-细胞界面下方的位置有关。这种细胞骨架重塑事件使 T 细胞内的分泌细胞器与 IS 对齐,从而使细胞因子和细胞毒性因子朝着 APC 定向释放。因此,MTOC 极化对于维持 T 细胞分泌和细胞毒性反应的特异性至关重要。一段时间以来,人们已经知道 T 细胞受体 (TCR) 刺激会激活 MTOC 极化反应。然而,很难确定将早期 TCR 信号与细胞骨架重塑偶联的机制。在过去的几年中,在这一领域取得了相当大的进展。本文将综述这方面的最新进展,涉及驱动 MTOC 极化的机制以及需要它的效应反应。特别关注蛋白激酶 C 家族的新成员和非典型成员,它们现在已知在极化状态的建立和维持中都起着重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94e6/3459186/d720375ac830/fimmu-03-00235-g001.jpg

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