Rho GTPase-mediated pathways in mature CD4+ T cells

被引:27
作者
Pernis, Alessandra B. [1 ]
机构
[1] Columbia Univ, Dept Med, New York, NY 10032 USA
关键词
Systemic Lupus Erythematosus (SLE); Guanine nucleotide exchange factor (GEF); Rho GTPase activating protein (GAP); Rho GDP-dissociation inhibitor (RhoGDI); IRF-4 Binding Protein (IBP); NUCLEOTIDE-EXCHANGE FACTOR; INDUCED APOPTOSIS; PKC-THETA; ACTIVATION; RAC; PROTEINS; TCR; LYMPHOCYTES; CYTOSKELETON; RESPONSES;
D O I
10.1016/j.autrev.2008.07.044
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Effective immune responses require the appropriate activation and differentiation of peripheral CD4(+) T cells. These processes need to be followed by the timely elimination of the responding T cells in order to restore T cell homeostasis. Defects in the appropriate regulation of T cell activation, expansion, and survival underlie the pathogenesis of many autoimmune disorders including SLE. The molecular machinery employed by T cells to properly control these processes and prevent the onset of autoimmunity has not been fully elucidated. Rho GTPases (which include the Rac, Cdc42, and Rho subfamilies) are molecular switches that control a wide range of cellular processes. Their fundamental role in biology is due to their ability to regulate both cytoskeletal dynamics and a large number of signal transduction pathways. Activation of Rho GTPases is now recognized as a key event in the coordination of immune responses and, particularly, in the activation of T cells. In this review, we will first provide an overview of the role of Rho GTPase-mediated pathways in mature CD4(+) T cells and then we will discuss recent studies, which suggest that deregulation of these pathways may play a role in the pathogenesis of SLE. (c) 2008 Published by Elsevier B.V.
引用
收藏
页码:199 / 203
页数:5
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