A critical role for the T cell receptor α-chain connecting peptide domain in positive selection of CD1-independent NKT cells

被引:0
|
作者
Capone, M
Troesch, M
Eberl, G
Hausmann, B
Palmer, E
MacDonald, HR
机构
[1] Univ Lausanne, Ludwig Inst Canc Res, Lausanne Branch, CH-1066 Epalinges, Switzerland
[2] Basel Inst Immunol, Basel, Switzerland
关键词
NKT cell; TCR transgenic mouse; MHC class II; alpha-connecting peptide;
D O I
10.1002/1521-4141(200106)31:6<1867::AID-IMMU1867>3.0.CO;2-B
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Natural killer T (NKT) cells are a subset of mature alpha beta TCR+ cells that co-express NK lineage markers. Whereas most NKT cells express a canonical V alpha 14/V beta8.2 TCR and are selected by CD1d, a minority of NKT cells express a diverse TCR repertoire and develop independently of CD1d. Little is known about the selection requirements of CD1d-independent NKT cells. We show here that NKT cells develop in RAG-deficient mice expressing an MHC class II-restricted transgenic TCR (V alpha2/V beta8.1) but only under conditions that lead to negative selection of conventional T cells. Moreover development of NKT cells in these mice is absolutely dependent upon an intact TCR alpha -chain connecting peptide domain, which is required for positive selection of conventional T cells via recruitment of the ERK signaling pathway. Collectively our data demonstrate that NKT cells can develop as a result of high avidity TCR/MHC class II interactions and suggest that common signaling pathways are involved in the positive selection of CD1d-independent NKT cells and conventional T cells.
引用
收藏
页码:1867 / 1875
页数:9
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