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
相关论文
共 21 条
[1]   Evidence for a link between sphingolipid metabolism and expression of CD1d and MHC-class II: monocytes from Gaucher disease patients as a model [J].
Balreira, A ;
Lacerda, L ;
Miranda, CS ;
Arosa, FA .
BRITISH JOURNAL OF HAEMATOLOGY, 2005, 129 (05) :667-676
[2]   Multiple defects in antigen presentation and T cell development by mice expressing cytoplasmic tail-truncated CDId [J].
Chiu, YH ;
Park, SH ;
Benlagha, K ;
Forestier, C ;
Jayawardena-Wolf, J ;
Savage, PB ;
Teyton, L ;
Bendelac, A .
NATURE IMMUNOLOGY, 2002, 3 (01) :55-60
[3]   The multiple sulfatase deficiency gene encodes an essential and limiting factor for the activity of sulfatases [J].
Cosma, MP ;
Pepe, S ;
Annunziata, I ;
Newbold, RF ;
Grompe, M ;
Parenti, G ;
Ballabio, A .
CELL, 2003, 113 (04) :445-456
[4]   Multiple sulfatase deficiency is caused by mutations in the gene encoding the human Cα-formylglycine generating enzyme [J].
Dierks, T ;
Schmidt, B ;
Borissenko, LV ;
Peng, JH ;
Preusser, A ;
Mariappan, M ;
von Figura, K .
CELL, 2003, 113 (04) :435-444
[5]   Impaired selection of invariant natural killer T cells in diverse mouse models of glycosphingolipid lysosomal storage diseases [J].
Gadola, Stephan D. ;
Silk, Jonathan D. ;
Jeans, Aruna ;
Illarionov, Petr A. ;
Salio, Mariolina ;
Besra, Gurdyal S. ;
Dwek, Raymond ;
Butters, Terry D. ;
Platt, Frances M. ;
Cerundolo, Vincenzo .
JOURNAL OF EXPERIMENTAL MEDICINE, 2006, 203 (10) :2293-2303
[6]   Autonomic denervation of lymphoid organs leads to epigenetic immune atrophy in a mouse model of Krabbe disease [J].
Galbiati, Francesca ;
Basso, Veronica ;
Cantuti, Ludovico ;
Givogri, Maria Irene ;
Lopez-Rosas, Aurora ;
Perez, Nicolas ;
Vasu, Chenthamarakshan ;
Cao, Hongmei ;
van Breemen, Richard ;
Mondino, Anna ;
Bongarzone, Ernesto R. .
JOURNAL OF NEUROSCIENCE, 2007, 27 (50) :13730-13738
[7]   MOLECULAR-GENETICS OF METACHROMATIC LEUKODYSTROPHY [J].
GIESELMANN, V ;
POLTEN, A ;
KREYSING, J ;
KAPPLER, J ;
FLUHARTY, A ;
VONFIGURA, K .
DEVELOPMENTAL NEUROSCIENCE, 1991, 13 (4-5) :222-227
[8]   Control points in NKT-cell development [J].
Godfrey, Dale I. ;
Berzins, Stuart P. .
NATURE REVIEWS IMMUNOLOGY, 2007, 7 (07) :505-518
[9]   Phenotype of arylsulfatase A-deficient mice: Relationship to human metachromatic leukodystrophy [J].
Hess, B ;
Saftig, P ;
Hartmann, D ;
Coenen, R ;
LullmannRauch, R ;
Goebel, HH ;
Evers, M ;
vonFigura, K ;
DHooge, R ;
Nagels, G ;
DeDeyn, P ;
Peters, C ;
Gieselmann, V .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14821-14826
[10]   Thymocyte expression of cathepsin L is essential for NKT cell development [J].
Honey, K ;
Benlagha, K ;
Beers, C ;
Forbush, K ;
Teyton, L ;
Kleijmeer, MJ ;
Rudensky, AY ;
Bendelac, A .
NATURE IMMUNOLOGY, 2002, 3 (11) :1069-1074