Regulation of T-cell receptor signaling by the actin cytoskeleton and poroelastic cytoplasm

被引:24
|
作者
Beemiller, Peter [1 ]
Krummel, Matthew F. [1 ]
机构
[1] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94148 USA
关键词
T cells; T-cell receptors; signal transduction; IMMUNOLOGICAL SYNAPSE FORMATION; MYOSIN-II INHIBITOR; ANTIGEN RECEPTOR; DENDRITIC CELLS; PLASMA-MEMBRANE; CUTTING EDGE; LYMPH-NODES; RETROGRADE FLOW; IN-VIVO; F-ACTIN;
D O I
10.1111/imr.12120
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 actin cytoskeleton plays essential roles in modulating T-cell activation. Most models of T-cell receptor (TCR) triggering signalosome assembly and immune synapse formation invoke actin-dependent mechanisms. As T cells are constitutively motile cells, TCR triggering and signaling occur against a cytoskeletal backdrop that is constantly remodeling. While the interplay between actin dynamics and TCR signaling have been the focus of research for many years, much of the work in T cells has considered actin largely for its scaffolding' function. We examine the roles of the actin cytoskeleton in TCR signaling and immune synapse formation with an emphasis on how poroelasticity, an ensemble feature of actin dynamics with the cytosol, relates to how T cells respond to stimulation.
引用
收藏
页码:148 / 159
页数:12
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