Huang Ching-Yu, Kanagawa Osami
Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO 63110, USA.
Eur J Immunol. 2004 Jun;34(6):1532-41. doi: 10.1002/eji.200424870.
CD4(-)CD8(-) thymocytes expressing a transgenic T cell receptor (TCR) alpha chain have decreased capacity to give rise to CD4(+)CD8(+) thymocytes when compared with wild-type thymocytes. This inefficient CD4(-)CD8(-) to CD4(+)CD8(+) maturation is mediated by the transgenic TCR alpha chain pairing with endogenous TCR beta chain but not with endogenous TCR gamma chain. Comparison between TCR alpha chain-transgenic mice with or without a functional pre-TCR alpha (pT alpha ) chain reveals that the formation of transgenic alpha/endogenous beta TCR on CD4(-)CD8(-) thymocytes inhibits the formation of pre-TCR, but at the same time mediates CD4(-)CD8(-) to CD4(+)CD8(+) maturation in the absence of pre-TCR, albeit inefficiently. These results indicate that alpha beta TCR and pre-TCR provide different signals for thymocyte development. They also suggest that the precise regulation of the sequential rearrangements of TCR beta and alpha loci and the cellular expansion induced by the pre-TCR may both be evolved to ensure the efficient generation of mature alpha beta T cells.
与野生型胸腺细胞相比,表达转基因T细胞受体(TCR)α链的CD4(-)CD8(-)胸腺细胞产生CD4(+)CD8(+)胸腺细胞的能力降低。这种低效的CD4(-)CD8(-)到CD4(+)CD8(+)成熟过程是由转基因TCRα链与内源性TCRβ链配对介导的,而不是与内源性TCRγ链配对。对具有或不具有功能性前TCRα(pTα)链的TCRα链转基因小鼠进行比较发现,CD4(-)CD8(-)胸腺细胞上转基因α/内源性β TCR的形成会抑制前TCR的形成,但同时在没有前TCR的情况下介导CD4(-)CD8(-)到CD4(+)CD8(+)的成熟,尽管效率不高。这些结果表明,αβ TCR和前TCR为胸腺细胞发育提供了不同的信号。它们还表明,TCRβ和α基因座的顺序重排以及前TCR诱导的细胞扩增的精确调控可能都是为了确保成熟αβ T细胞的有效产生而进化而来的。