Lipid binding orientation within CD1d affects recognition of Borrelia burgorferi antigens by NKT cells

被引:79
作者
Wang, Jing [1 ]
Li, Yali [1 ]
Kinjo, Yuki [2 ]
Mac, Thien-Thi [1 ]
Gibson, Darren [3 ]
Painter, Gavin F. [3 ]
Kronenberg, Mitchell [2 ]
Zajonc, Dirk M. [1 ]
机构
[1] La Jolla Inst Allergy & Immunol, Div Cell Biol, La Jolla, CA 92037 USA
[2] La Jolla Inst Allergy & Immunol, Div Dev Immunol, La Jolla, CA 92037 USA
[3] Ind Res Ltd, Carbohydrate Chem Team, Lower Hutt 6008, New Zealand
关键词
microbial glycolipids; immune evasion; lyme disease; KILLER T-CELLS; ALPHA-GALACTOSYLCERAMIDE; CRYSTAL-STRUCTURE; STRUCTURAL BASIS; HIGH-AFFINITY; MOUSE CD1D; GLYCOLIPIDS; ACTIVATION; RECEPTOR; COMPLEX;
D O I
10.1073/pnas.0909479107
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Invariant natural killer T cells (iNKT cells) respond to CD1d-presented glycolipids from Borrelia burgdorferi, the causative agent of Lyme disease. Although mouse and human iNKT cells respond to different antigens based on subtle differences in their fatty acids, the mechanism by which fatty acid structuredeterminesantigenicpotency is not well understood. Here we show that the mouse and human CD1d present glycolipids having different fatty acids, based in part upon a difference at a single amino acid position that is involved in positioning the sugar epitope. CD1d also can bind nonantigenic lipids, however, but unexpectedly, mouse CD1d orients the two aliphatic chains of a nonantigenic lipid rotated 180 degrees, causing a dramatic repositioning of the exposed sugar. Therefore, our data reveal the biochemical basis for the high degree of antigenic specificity of iNKT cells for certain fatty acids, and they suggest how microbes could alter fatty acid biosynthesis as an immune evasion mechanism.
引用
收藏
页码:1535 / 1540
页数:6
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