Agonist-induced T cell receptor down-regulation: Molecular requirements and dissociation from T cell activation

被引:59
|
作者
Salio, M
Valitutti, S
Lanzavecchia, A
机构
[1] Basel Institute for Immunology, Basel
[2] Basel Institute for Immunology, CH-4005, Basel
关键词
T lymphocyte; T cell receptor down-regulation; protein tyrosine kinase inhibitor;
D O I
10.1002/eji.1830270726
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T cell receptor (TCR) down-regulation is a consequence of specific receptor engagement and plays an important role in modulating the T cell response. We have investigated the role of protein kinase C (PKC) and protein tyrosine kinases (PTK) in the induction of TCR down-regulation. We report that the mutation of S126 in the CD3-gamma chain that is known to inhibit phorbol-12-myristate 13-acetate-induced TCR down-regulation does not affect down-regulation induced by a specific agonist. In addition, agonist-induced TCR down-regulation is not affected by blockade or depletion of PKC, neither by blockade or lack of PTK, while the same treatments efficiently interfere with T cell activation. These results demonstrate that TCR down-regulation is induced by early events which follow specific engagement by an agonist and can be dissociated from those required for full T cell activation.
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页码:1769 / 1773
页数:5
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