Differences in the ligand specificity between CD1d-restricted T cells with limited and diverse T-cell receptor repertoire

被引:0
|
作者
Makowska, A
Kawano, T
Taniguchi, M
Cardell, S
机构
[1] Univ Lund, Dept Cell & Mol Biol, Immunol Sect, S-22362 Lund, Sweden
[2] Chiba Univ, Grad Sch Med, Dept Mol Immunol, Chuo Ku, Chiba 260, Japan
关键词
D O I
暂无
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 natural killer (NK) T-lymphocyte population consists of two subsets utilizing a diverse and restricted T-cell receptor (TCR) repertoire, respectively. Both populations have been shown to include autoreactive cells. NKT cells carrying restricted V alpha 14(AV14S1)J alpha 281/V beta 8.2(BV8S2A1) TCR have been shown to recognize alpha-galactosylceramide (alpha GalCer) presented in the context of murine CD1d. In this study we screened a set of murine CD1d-autoreactive T-cell hybridomas with diverse TCR for their reactivity with several glycosylated variants of ceramide, including alpha GalCer. These hybridomas showed a different pattern of reactivity to CD1d-expressing antigen-presenting cells (APC) and were not reactive with any of the tested variants of ceramide. A second set of hybridomas had been selected for expression of V alpha 14 and V beta 8.2 TCR chains. These cells responded to alpha GalCer presented on CD1d, but were only weakly reactive to syngeneic splenocytes or CD1d-transfected cells. Their fine specificity in the response to glycosylation variants of ceramide demonstrated a homogenous reactivity pattern, including reactivity to alpha-galactosylsphingosine, the variant of alpha GalCer with truncated fatty acyl chain. These findings underline the differences in ligand specificity between the two subsets of CD1d-restricted NKT cells, and demonstrate a similarity in reactivity among the hybridomas using the V alpha 14-J alpha 281/V beta 8.2 TCR.
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页码:71 / 79
页数:9
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