Receptor Signaling Clusters in the Immune Synapse

被引:170
作者
Dustin, Michael L. [1 ,2 ]
Groves, Jay T. [3 ,4 ]
机构
[1] NYU, Sch Med, Skirball Inst Biomol Med, Program Mol Pathogenesis, New York, NY 10016 USA
[2] NYU, Sch Med, Dept Pathol, New York, NY 10016 USA
[3] Univ Calif Berkeley, Dept Chem, Howard Hughes Med Inst, Berkeley, CA 94720 USA
[4] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Phys Biosci Div, Berkeley, CA 94720 USA
来源
ANNUAL REVIEW OF BIOPHYSICS, VOL 41 | 2012年 / 41卷
关键词
cytoskeleton; signal transduction; spatial mutation; T-CELL-ACTIVATION; SUPPORTED PLANAR BILAYERS; ANTIGEN-PRESENTING CELL; KINASE-C-THETA; IMMUNOLOGICAL SYNAPSE; CUTTING EDGE; PEPTIDE COMPLEXES; DENDRITIC CELLS; MINIMAL NUMBER; LIPID-BILAYERS;
D O I
10.1146/annurev-biophys-042910-155238
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Signaling processes between various immune cells involve large-scale spatial reorganization of receptors and signaling molecules within the cell-cell junction. These structures, now collectively referred to as immune synapses, interleave physical and mechanical processes with the cascades of chemical reactions that constitute signal transduction systems. Molecular level clustering, spatial exclusion, and long-range directed transport are all emerging as key regulatory mechanisms. The study of these processes is drawing researchers from physical sciences to join the effort and represents a rapidly growing branch of biophysical chemistry. Recent advances in physical and quantitative analyses of signaling within the immune synapses are reviewed here.
引用
收藏
页码:543 / 556
页数:14
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