TRPC3 mediates T-cell receptor-dependent calcium entry in human T-lymphocytes

被引:108
|
作者
Philipp, S
Strauss, B
Hirnet, D
Wissenbach, U
Méry, L
Flockerzi, V
Hoth, M
机构
[1] Univ Saarland, Inst Expt & Klin Pharmakol & Toxikol, D-66421 Homburg, Germany
[2] Univ Saarland, Inst Physiol, D-66421 Homburg, Germany
关键词
D O I
10.1074/jbc.M304044200
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
Stimulation of the T-cell receptor (TCR) activates Ca2+ entry across the plasma membrane, which is a key triggering event for the T-cell-associated immune response. We show that TRPC3 channels are important for the TCR-dependent Ca2+ entry pathway. The TRPC3 gene was found to be damaged in human T-cell mutants defective in Ca2+ influx. Mutations of the TRPC3 gene were accompanied by changes of TRPC3 gene expression. Introduction of the complete human TRPC3 cDNA into those mutants rescued Ca2+ currents as well as TCR-dependent Ca2+ signals. Our data provide the initial step toward understanding the molecular nature of endogenous Ca2+ channels participating in T-cell activation and put forward TRPC3 as a new target for modulating the immune response.
引用
收藏
页码:26629 / 26638
页数:10
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