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

被引:61
|
作者
Sancho, D [1 ]
Vicente-Manzanares, M [1 ]
Mittelbrunn, M [1 ]
Montoya, MC [1 ]
Gordón-Alonso, M [1 ]
Serrador, JM [1 ]
Sánchez-Madrid, F [1 ]
机构
[1] Univ Autonoma Madrid, Hosp Princesa, Serv Inmunol, Madrid 28006, Spain
关键词
D O I
10.1034/j.1600-065X.2002.18908.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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.
引用
收藏
页码:84 / 97
页数:14
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