Actin cytoskeletal dynamics in T lymphocyte activation and migration

被引:143
作者
Samstag, Y [1 ]
Eibert, SM [1 ]
Klemke, M [1 ]
Wabnitz, GH [1 ]
机构
[1] Heidelberg Univ, Inst Immunol, D-69120 Heidelberg, Germany
关键词
costimulation; cofilin; L-plastin; enhanced actin polymerization; immunological synapse;
D O I
10.1189/jlb.0602272
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Dynamic rearrangements of the actin cytoskeleton are crucial for the function of numerous cellular elements including T lymphocytes. They are required for migration of T lymphocytes through the body to scan for the presence of antigens, as well as for the formation and stabilization of the immunological synapse at the interface between antigen-presenting cells and T lymphocytes. Supramolecular activation clusters within the immunological synapse play an important role for the initiation of T cell responses and for the execution of T cell effector functions. In addition to the T cell receptor/CD3 induced actin nucleation via Wasp/Arp2/3-activation, signals through accessory receptors of the T cell (i.e., costimulation) regulate actin cytoskeletal dynamics. In this regard, the actin-binding proteins cofilin and L-plastin represent prominent candidates linking accessory receptor stimulation to the rearrangement of the actin cytoskeleton. Cofilin enhances actin polymerization via its actin-severing activity, and as a longlasting effect, cofilin generates novel actin monomers through F-actin depolymerization. L-plastin stabilizes actin filament structures by means of its actin-bundling activity.
引用
收藏
页码:30 / 48
页数:19
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