Asymmetric ligand recognition by the activating natural killer cell receptor NKG2D, a symmetric homodimer

被引:48
作者
Strong, RK [1 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
关键词
natural killer cell receptors; NKG2D; MICA; RAE-1; reecptor-ligand recognition; structural immunology;
D O I
10.1016/S0161-5890(02)00032-9
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Natural killer (NK) cells function through a diverse array of cell-surface natural killer receptors (NCRs). NCRs specific for classical and non-classical MHC class I proteins, expressed in complex patterns of inhibitors and activating isoforms on overlapping. but distinct. subsets of NK cells, play an important role in immunosurveillance against cells that have reduced MHC class I expression as a result of infection or transformation. Another NCR. NKG2D. is an activating NCR first identified on NK cells, but subsequently found on macrophages and a variety of T cell types. NKG2D ligands in rodents include the MHC class I-like proteins RAE-1 and H60 and, in humans, ULBPs and the cell stress-inducible proteins MICA and MICB. NKG2D-MICA and -RAE-1 recognition events have been implicated in anti-viral and -tumor immune responses. Crystallographic analyses of NKG2D-MICA and -RAE-1 complexes reveal an unusual mode of recognition that apparently tolerates a surprising degree of ligand plasticity while generating affinities that are among the strongest TCR- or NCR-ligand affinities. thus, far described. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
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页码:1029 / 1037
页数:9
相关论文
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