Characterization of the ovalbumin-specific TCR transgenic line OT-I: MHC elements for positive and negative selection

被引:234
作者
Clarke, SRM
Barnden, M
Kurts, C
Carbone, FR
Miller, JF
Heath, WR
机构
[1] Royal Melbourne Hosp, Div Immunol, Walter & Eliza Hall Inst, Melbourne, Vic 3050, Australia
[2] Alfred Hosp, Monash Med Sch, Dept Pathol & Immunol, Prahran, Vic 3181, Australia
[3] Queensland Inst Med Res, Cooperat Res Ctr Vaccine Technol, Herston, Qld 4006, Australia
关键词
CD8(+) T lymphocyte; cytotoxic T lymphocyte; ovalbumin; thymus; transgenic T cell receptor;
D O I
10.1046/j.1440-1711.2000.00889.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The present report provides the first extensive characterization of the OT-I TCR transgenic line, which produces MHC class I-restricted, ovalbumin-specific, CD8(+) T cells (OT-I cells). These cells an shown to be positively selected in vivo in H-2(b) C57BL/6 mice and in bm5 mice, which express the K-bm5 mutant molecule. In contrast, OT-I cells were not selected by mutant K-b molecules in bm1,bm3, bm8, bm10, bm11 or bm23 mice. Interestingly, however, when positive selection was examined in vitro in foetal thymic organ culture (FTOC), bm1 and bm8 were still poorly selective, but the bm3 haplotype now selected as efficiently as B6. The ability to select in vitro correlated with the capacity to present the ovalbumin (OVA) peptide to OT-I cells, as measured by induction of an OVA-specific proliferative response. These results suggest that a lower affinity TCR:MMC interaction may be necessary for positive selection in FTOC compared with selection in situ.
引用
收藏
页码:110 / 117
页数:8
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