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免疫相互作用过程中微管组织中心方向的调控及肌动球蛋白细胞骨架重排

Regulation of microtubule-organizing center orientation and actomyosin cytoskeleton rearrangement during immune interactions.

作者信息

Sancho David, Vicente-Manzanares Miguel, Mittelbrunn María, Montoya María C, Gordón-Alonso Mónica, Serrador Juan M, Sánchez-Madrid Francisco

机构信息

Servicio de Inmunología, Hospital de la Princesa, Universidad Autónoma de Madrid, Madrid, Spain.

出版信息

Immunol Rev. 2002 Nov;189:84-97. doi: 10.1034/j.1600-065x.2002.18908.x.

Abstract

The reorganization of membrane, cytoskeletal and signaling molecules during immune interactions is critical for the generation of immune response. At the initiation of the T cell-antigen presenting cell (APC) interaction, antigen-independent weak adhesion forces allow the scanning of the APC surface by the T cell receptor for specific antigens. The stabilization of T cell-APC conjugates involves the segregation of membrane and intracellular signaling proteins, driven by reorganization of membrane microdomains and cytoskeletal changes. In early T cell-APC cognate interactions, the microtubular cytoskeleton undergoes drastic changes that lead to microtubule-organizing center (MTOC) reorientation to the vicinity of the cell-cell contact area. Recent data on the dynamics of MTOC redistribution and its influence in T cell-APC conjugate stabilization, together with the description of an increasing number of signaling molecules associated to this complex, underscore the key role of MTOC translocation in the T cell response. We focus on the mechanisms that control the early MTOC reorientation during T cell-APC interaction and the relevance of this process to T cell activation.

摘要

免疫相互作用过程中膜、细胞骨架和信号分子的重组对于免疫反应的产生至关重要。在T细胞与抗原呈递细胞(APC)相互作用开始时,抗原非依赖性的弱粘附力使T细胞受体能够扫描APC表面以寻找特定抗原。T细胞与APC结合物的稳定涉及膜和细胞内信号蛋白的分离,这是由膜微结构域的重组和细胞骨架变化驱动的。在早期T细胞与APC的同源相互作用中,微管细胞骨架会发生剧烈变化,导致微管组织中心(MTOC)重新定位到细胞-细胞接触区域附近。关于MTOC重新分布的动力学及其对T细胞与APC结合物稳定的影响的最新数据,以及与该复合物相关的越来越多信号分子的描述,都强调了MTOC易位在T细胞反应中的关键作用。我们关注控制T细胞与APC相互作用过程中早期MTOC重新定位的机制以及该过程与T细胞活化的相关性。

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