Vγ9/Vδ2 T cell activation induced by bacterial low molecular mass compounds depends on the 1-deoxy-D-xylulose 5-phosphate pathway of isoprenoid biosynthesis

被引:78
作者
Jomaa, H
Feurle, J
Lühs, K
Kunzmann, V
Tony, HP
Herderich, M
Wilhelm, M
机构
[1] Univ Wurzburg, Med Poliklin, D-97070 Wurzburg, Germany
[2] Univ Wurzburg, Lehrstuhl Lebensmittelchem, D-97074 Wurzburg, Germany
来源
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY | 1999年 / 25卷 / 04期
关键词
gamma delta T cells; isoprenoid biosynthesis; isopentenyl diphosphate;
D O I
10.1016/S0928-8244(99)00110-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Isopentenyl diphosphate (IPP), an important precursor of isoprenoid biosynthesis in prokaryotic and eukaryotic organisms, has been shown to activate V gamma 9/V delta 2 T cells, the major subset of human gamma delta T cells. The biosynthesis of IPP has been first described as the acetate/mevalonate pathway. Recently, 1-deoxy-D-xylulose 5-phosphate (DOXP) and 2-C-methyl-D-erythritol 4-phosphate have been shown to be key metabolites in the DOXP pathway also leading to the formation of IPP in some eubacteria such as Escherichia coli. Here we report that the low molecular mass fraction of extracts from bacteria using the DOXP pathway induces V gamma 9/V delta 2 T cell activation, while analogous preparations from bacteria using the classical mevalonate pathway fail to do so. Addition of 1-deoxy-D-xylulose potentiates the ability of E. coli extracts to activate V gamma 9/V delta 2 T cells. As the amounts of IPP present in the bacterial preparations are not sufficient to induce significant V gamma 9/V delta 2 T cell activation, our data suggest that compounds other than IPP associated with the DOXP pathway are responsible for V gamma 9/V delta 2 T cell activation. (C) 1999 Federation of European Microbiological Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:371 / 378
页数:8
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