Implications for invariant natural killer T cell ligands due to the restricted presence of isoglobotrihexosylceramide in mammals

被引:124
作者
Speak, Anneliese O.
Salio, Mariolina
Neville, David C. A.
Fontaine, Josette
Priestman, David A.
Platt, Nick
Heare, Tanya
Butters, Terry D.
Dwek, Raymond A.
Trottein, Francois
Exley, Mark A.
Cerundolo, Vincenzo
Platt, Frances M.
机构
[1] Univ Oxford, Dept Pharmacol, Oxford OX1 3QT, England
[2] John Radcliffe Hosp, Weatherall Inst Mol Med, Tumor Immunol Grp, Oxford OX3 9DS, England
[3] Univ Oxford, Dept Biochem, Inst Glycobiol, Oxford OX1 3QU, England
[4] Inst Pasteur, INSERM, U547, F-59019 Lille, France
[5] Univ Southampton, Sch Biol Sci, Southampton SO16 7PX, Hants, England
[6] Harvard Univ, Beth Israel Deaconess Med Ctr, Sch Med, Div Haematol & Oncol, Boston, MA 02215 USA
基金
英国医学研究理事会;
关键词
glycosphingolipid; thymus; CD1d; lipid presentation;
D O I
10.1073/pnas.0607285104
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
Development of invariant natural killer T (iNKT) cells requires the presentation of lipid ligand(s) by CD1d molecules in the thymus. The glycosphingolipid (GSL) isoglobotrihexosylceramide (iGb3) has been proposed as the natural iNKT cell-selecting ligand in the thymus and to be involved in peripheral activation of iNKT cells by dendritic cells (DCs). However, there is no direct biochemical evidence for the presence of iGb3 in mouse or human thymus or DCs. Using a highly sensitive HPLC assay, the only tissue where iGb3 could be detected in mouse was the dorsal root ganglion (DRG). iGb3 was not detected in other mouse or any human tissues analyzed, including thymus and DCs. Even in mutant mice that store isoglobo-series GSLs in the DRG, we were still unable to detect these GSLs in the thymus. iGb3 is therefore unlikely to be a physiologically relevant iNKT cell-selecting ligand in mouse and humans. A detailed study is now warranted to better understand the nature of iNKT cell-selecting ligand(s) in vivo.
引用
收藏
页码:5971 / 5976
页数:6
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