Kirberg J, Baron A, Jakob S, Rolink A, Karjalainen K, von Boehmer H
Basel Institute for Immunology, Switzerland.
J Exp Med. 1994 Jul 1;180(1):25-34. doi: 10.1084/jem.180.1.25.
We describe mice that express a transgenic T cell receptor alpha/beta (TCR-alpha/beta) specific for peptide 111-119 from influenza hemagglutinin presented by I-Ed class II major histocompatibility complex (MHC) molecules. The transgenic TCR is expressed on CD4+8- as well as CD4-8+ mature T cells even in mice that are deficient in rearrangement or do not express endogenous TCR-alpha genes. The CD4-8+ T cells require I-Ed class II MHC molecules for positive selection and can be activated to proliferate and to kill by I-Ed molecules presenting the relevant peptide. Full maturation of these cells, however, also requires the presence of class I MHC molecules. The results are compatible with the notion that T cell maturation requires multiple receptor-ligand interactions and establish an exception to the rule that class II-restricted TCRs are exclusively expressed by mature CD4+8- cells.
我们描述了这样的小鼠,其表达一种转基因α/β型T细胞受体(TCR-α/β),该受体对由Ⅱ类主要组织相容性复合体(MHC)分子I-E d呈递的流感血凝素肽111 - 119具有特异性。即使在缺乏重排或不表达内源性TCR-α基因的小鼠中,转基因TCR也在CD4 + 8 -以及CD4 - 8 +成熟T细胞上表达。CD4 - 8 + T细胞需要I-E dⅡ类MHC分子进行阳性选择,并且可以被呈递相关肽的I-E d分子激活而增殖并杀伤。然而,这些细胞的完全成熟也需要Ⅰ类MHC分子的存在。这些结果与T细胞成熟需要多种受体 - 配体相互作用的观点相符,并为Ⅱ类限制性TCR仅由成熟CD4 + 8 -细胞表达这一规则建立了一个例外。