Development and maturation of invariant NKT cells in the presence of lysosomal engulfment

被引:12
|
作者
Plati, Tiziana [1 ]
Visigalli, Ilaria [1 ]
Capotondo, Alessia [1 ,2 ]
Buono, Mario [3 ]
Naldini, Luigi [1 ,2 ]
Cosma, Maria Pia [3 ]
Biffi, Alessandra [1 ]
机构
[1] San Raffaele Telethon Inst Gene Therapy, San Raffaele Sci Inst, I-20132 Milan, Italy
[2] Univ Vita Salute San Raffaele, San Raffaele Sci Inst, Milan, Italy
[3] Telethon Inst Genet & Med, Naples, Italy
关键词
Invariant NKT cells; Lysosomal storage disorders; Selecting ligand; MULTIPLE SULFATASE DEFICIENCY; KILLER T-CELLS; ANTIGEN PRESENTATION; MOLECULAR-GENETICS; MOUSE MODEL; DISEASE; MICE; ISOGLOBOTRIHEXOSYLCERAMIDE; CD1D;
D O I
10.1002/eji.200939639
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A defect in invariant NKT (iNKT) cell selection was hypothesized in lysosomal storage disorders (LSD). Accumulation of glycosphingolipids (GSL) in LSD could influence lipid loading and/or presentation causing entrapment of endogenous ligand(s) within storage bodies or competition of the selecting ligand(s) by stored lipids for CD1d binding. However, when we analyzed the iNKT cell compartment in newly tested LSD animal models that accumulate GSL, glycoaminoglycans or both, we observed a defective iNKT cell selection only in animals affected by multiple sulfatase deficiency, in which a generalized aberrant T-cell development, rather than a pure iNKT defect, was present. Mice with single lysosomal enzyme deficiencies had normal iNKT cell development. Thus, GSL/glycoaminoglycans storage and lysosomal engulfment are not sufficient for affecting iNKT cell development. Rather, lipid ligand(s) or storage compounds, which are affected in those LSD lacking mature iNKT cells, might indeed be relevant for iNKT cell selection.
引用
收藏
页码:2748 / 2754
页数:7
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