Regulation of cytoskeletal dynamics at the immune synapse: New stars join the actin troupe

被引:59
作者
Billadeau, Daniel D.
Burkhardt, Janis K. [1 ]
机构
[1] Childrens Hosp Philadelphia, Dept Pathol & Lab Med, Philadelphia, PA 19104 USA
[2] Mayo Clin, Coll Med, Dept Immunol, Rochester, MN 55905 USA
[3] Mayo Clin, Coll Med, Div Oncol Res, Rochester, MN 55905 USA
[4] Univ Penn, Philadelphia, PA 19104 USA
关键词
actin; cofilin; HS1; immune synapse; signaling; T cell; VASP; WASp; WAVE; WIP;
D O I
10.1111/j.1600-0854.2006.00491.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Reorganization of actin cytoskeletal dynamics plays a critical role in controlling T-lymphocyte activation and effector functions. Interaction of T-cell receptors (TCR) with appropriate major histocompatability complex-peptide complexes on antigen-presenting cells results in the activation of signaling cascades, leading to the accumulation of F-actin at the cell-cell contact site. This event is required for the formation and stabilization of the immune synapse (IS), a cellular structure essential for the modulation of T-cell responses. Analysis of actin cytoskeletal dynamics following engagement of the TCR has largely focused on the Arp2/3 regulator, WASp, because of its early identification and its association with human disease. However, recent studies have shown equally important roles for several additional actin regulatory proteins. In this review, we turn the spotlight on the expanding cast of actin regulatory proteins, which co-ordinate actin dynamics at the IS.
引用
收藏
页码:1451 / 1460
页数:10
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