LAT displacement from lipid rafts as a molecular mechanism for the inhibition of T cell signaling by polyunsaturated fatty acids

被引:135
作者
Zeyda, M
Staffler, G
Horejsí, V
Waldhäusl, W
Stulnig, TM
机构
[1] Univ Vienna, Dept Internal Med 3, A-1090 Vienna, Austria
[2] Univ Vienna, Inst Immunol, A-1090 Vienna, Austria
[3] Acad Sci Czech Republ, Inst Mol Genet, CR-14220 Prague, Czech Republic
关键词
D O I
10.1074/jbc.M203343200
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
Polyunsaturated fatty acids (PUFAs) suppress immune responses and inhibit T cell activation through largely unknown mechanisms. The displacement of signaling proteins from membrane lipid rafts has recently been suggested as underlying PUFA-mediated T cell inhibition. We show here that PUFA treatment specifically interferes with T cell signal transduction by blocking tyrosine phosphorylation of LAT (linker for activation of T cells) and phospholipase Cgamma1. A significant fraction of IAT was displaced from rafts by PUFA treatment along with other signaling proteins. However, retaining LAT alone in lipid rafts effectively restored phospholipase Cgamma1/calcium. signaling in PUFA-treated T cells. These data reveal LAT displacement from lipid rafts as a molecular mechanism by which PUFAs inhibit T cell signaling and underline the predominant importance of ILAT localization in rafts for efficient T cell activation.
引用
收藏
页码:28418 / 28423
页数:6
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