Distinct Requirements for CD1d Intracellular Transport for Development of Vα14 iNKT Cells

被引:9
|
作者
Sille, Fenna C. M. [1 ,2 ,3 ]
Boxem, Mike [4 ]
Sprengers, Dave [2 ,3 ,5 ]
Veerapen, Natacha [6 ]
Besra, Gurdyal [6 ]
Boes, Marianne [1 ,2 ,3 ]
机构
[1] Wilhelmina Childrens Hosp, Univ Med Ctr Utrecht, Dept Pediat Immunol, Utrecht, Netherlands
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] Brigham & Womens Hosp, Dept Dermatol, Boston, MA 02115 USA
[4] Univ Utrecht, Dept Dev Biol, Utrecht, Netherlands
[5] Erasmus MC, Dept Gastroenterol & Hepatol, Rotterdam, Netherlands
[6] Univ Birmingham, Sch Biosci, Birmingham, W Midlands, England
来源
JOURNAL OF IMMUNOLOGY | 2009年 / 183卷 / 03期
基金
英国医学研究理事会; 英国惠康基金;
关键词
KILLER T-CELLS; CLASS-I MOLECULES; CD1D-RESTRICTED NKT CELLS; DENDRITIC CELLS; ALPHA-GALACTOSYLCERAMIDE; ANTIGEN PRESENTATION; CORTICAL THYMOCYTES; POSITIVE SELECTION; MICE; LINEAGE;
D O I
10.4049/jimmunol.0901354
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The positive selection of V alpha 14 invariant (i)NKT cells in mice requires CD1d-mediated Ag presentation by CD4(+)CD8(+) thymocytes. Maturation of newly selected iNKT cells continues in the periphery and also involves CD1d expression. CD1d molecules acquire Ags for presentation in endosomal compartments, to which CD1d molecules have access through an intrinsic CD1d-encoded tyrosine motif and by association with the class II MHC chaperone, invariant chain. In this study, we report the generation of mice in which all CD1d is replaced by CD1d-enhanced yellow fluorescent fusion protein (EYFP). CD1d-EYFP molecules are stable, present lipid Ags, and have near normal subcellular distribution. CD1d-EYFP molecules mediated positive selection of V alpha 14 iNKT cell precursors at decreased efficiency, caused a delay in their terminal maturation, and did not invoke V alpha 14 iNKT cell effector function as wild-type CD1d could. Using these mice, we show that the intrinsic CD1d-encoded sorting motif mediates thymic selection and activation of V alpha 14 iNKT cells by professional APCs, while for peripheral terminal differentiation the intrinsic CD1d sorting motif is dispensable. The Journal of Immunology, 2009, 183: 1780-1788.
引用
收藏
页码:1780 / 1788
页数:9
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