Forming a Complex with MHC Class I Molecules Interferes with Mouse CD1d Functional Expression

被引:3
作者
Gourapura, Renukaradhya J. [1 ]
Khan, Masood A. [1 ]
Gallo, Richard M. [1 ]
Shaji, Daniel [1 ]
Liu, Jianyun [1 ]
Brutkiewicz, Randy R. [1 ]
机构
[1] Indiana Univ Sch Med, Dept Microbiol & Immunol, Indianapolis, IN 46202 USA
来源
PLOS ONE | 2013年 / 8卷 / 08期
关键词
CD1D-MEDIATED ANTIGEN PRESENTATION; T-CELL RECOGNITION; SURFACE; INHIBITION; RECEPTORS; BINDING; MICE; LY49; GLYCOLIPIDS; TRAFFICKING;
D O I
10.1371/journal.pone.0072867
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
CD1d molecules are structurally similar to MHC class I, but present lipid antigens as opposed to peptides. Here, we show that MHC class I molecules physically associate with (and regulate the functional expression of) mouse CD1d on the surface of cells. Low pH (3.0) acid stripping of MHC class I molecules resulted in increased surface expression of murine CD1d on antigen presenting cells as well as augmented CD1d-mediated antigen presentation to NKT cells. Consistent with the above results, TAP1-/- mice were found to have a higher percentage of type I NKT cells as compared to wild type mice. Moreover, bone marrow-derived dendritic cells from TAP1-/- mice showed increased antigen presentation by CD1d compared to wild type mice. Together, these results suggest that MHC class I molecules can regulate NKT cell function, in part, by masking CD1d.
引用
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页数:11
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