Lck and the nature of the T cell receptor trigger

被引:43
作者
Davis, Simon J. [1 ,2 ]
van der Merwe, P. Anton [3 ]
机构
[1] Univ Oxford, Oxford Radcliffe Hosp, Nuffield Dept Clin Med, Oxford OX3 9DS, England
[2] Univ Oxford, Oxford Radcliffe Hosp, Med Res Council Human Immunol Unit, Weatherall Inst Mol Med, Oxford OX3 9DS, England
[3] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
TYROSINE-PROTEIN-KINASE; SEGREGATION MODEL; STRUCTURAL BASIS; CD45; ACTIVATION; TCR; COMPLEX; PHOSPHATASES; RECOGNITION; CD2;
D O I
10.1016/j.it.2010.11.003
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Exactly how ligand binding 'triggers' T cell receptor (TCR) phosphorylation is unclear. It has been proposed that ligand engagement by the TCR somehow activates the Src kinase Lck, which in turn phosphorylates the receptor. Recent data, however, suggest instead that a significant fraction of the Lck in resting T cells is already activated and that the proportion of active Lck does not change during the early stages of T cell activation. We argue that, caveats notwithstanding, these new observations offer support for the 'kinetic-segregation' model of TCR triggering, which involves spatial reorganization of signalling proteins upon ligand binding and requires a fraction of Lck to be active in resting T cells.
引用
收藏
页码:1 / 5
页数:5
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