Billadeau Daniel D, Burkhardt Janis K
Department of Immunology and Division of Oncology Research, Mayo Clinic College of Medicine, Rochester, MN 55905, USA.
Traffic. 2006 Nov;7(11):1451-60. doi: 10.1111/j.1600-0854.2006.00491.x. Epub 2006 Sep 19.
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 histocompatibility 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.
肌动蛋白细胞骨架动力学的重组在控制T淋巴细胞活化和效应器功能中起着关键作用。T细胞受体(TCR)与抗原呈递细胞上适当的主要组织相容性复合体 - 肽复合物相互作用会导致信号级联反应的激活,从而导致F - 肌动蛋白在细胞 - 细胞接触部位积累。这一事件是免疫突触(IS)形成和稳定所必需的,免疫突触是调节T细胞反应所必需的细胞结构。由于TCR参与后对肌动蛋白细胞骨架动力学的分析在很大程度上集中在Arp2/3调节因子WASp上,因为它被早期鉴定且与人类疾病有关。然而,最近的研究表明几种其他肌动蛋白调节蛋白也起着同样重要的作用。在这篇综述中,我们将重点关注不断增加的肌动蛋白调节蛋白,它们在免疫突触处协调肌动蛋白动力学。