Expression of functional GPR35 in human iNKT cells

被引:98
作者
Fallarini, Silvia [1 ]
Magliulo, Laura [1 ]
Paoletti, Tiziana [1 ]
de Lalla, Claudia [2 ]
Lombardi, Grazia [1 ]
机构
[1] Univ Piemonte Orientale Amedeo Avogadro, Dipartimento Sci Chim Alimentari Farmaceut & Farm, I-28100 Novara, Italy
[2] Ist Sci San Raffaele, Canc Immunotherapy & Gene Therapy Program, Expt Immunol Unit, DIBIT, I-20132 Milan, Italy
关键词
GPR35; Human iNKT cells; Cytokines; Kynurenic acid; INVARIANT NKT CELLS; PROTEIN-COUPLED RECEPTOR; KILLER T-CELLS; KYNURENINE PATHWAY; IFN-GAMMA; ACID; DIFFERENTIATION; IDENTIFICATION; METABOLISM; MODULATION;
D O I
10.1016/j.bbrc.2010.06.091
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The aim of this study was to examine the expression of G protein-coupled receptor (GPR)35 in human invariant natural killer T (iNKT) cells and to determine the functional effects induced by selective activation of this receptor. RT-PCR analysis showed that both human iNKT cells and resting PBMC expressed GPR35: GPR35 protein resulted mostly localized in the plasma membrane, while it internalized in punctate intracellular structures following specific receptor activation (Western blot and immunofluorescence/confocal microscopy analysis). The specific activation of GPR35 by selective receptor agonists kynurenic acid (KYNA)] or 1,4-dihydro-5-(2-propoxyphenyl)-7H-1,2,3-triazolo 14,5-d]pyrimidine-7-one (zaprinast)] functionally correlated with a significant reduction in IL-4 release from alpha-galactosylceramide (alpha-GalCer)-activated human iNKT cells, and this effect resulted mediated by pertussis toxin (PTX)-sensitive Gi/o proteins. In conclusion, our results demonstrate that human iNKT cells express GPR35 functionally active in reducing IL-4 release. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:420 / 425
页数:6
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