Mazda O, Aiba Y, Hattori N, Li M, Fujimoto S, Davis M M, Katsura Y
Department of Immunology, Chest Disease Research Institute, Kyoto University, Japan.
Immunol Invest. 1995 Nov;24(6):927-46. doi: 10.3109/08820139509060718.
The expression of endogenous T cell receptor (TcR) beta chains in a TcR beta chain gene transgenic mouse (TGM) strain was examined. Unlike many other TGM strains reported, a considerable proportion of T cells from the thymus and spleen as well as organ cultured fetal thymus from our TGM express endogenous TCR beta chains on their surface. Compatible with this was the elucidation of VDJ rearrangement of endogenous beta chain genes by PCR. Three color flow cytometric analysis of thymus cell subpopulations revealed that the expression levels of both endogenous and transgenic TcR beta genes are regulated in a maturational stage specific manner. Splenic T cells contained a several fold higher percentage of endogenous TcR beta positive cells than thymus cells, suggesting a role of TcR on T cell peripherization. V beta 6 positive cells were deleted in the TGM carrying minor lymphocyte stimulating (Mls)-la antigen, indicating that the endogenous TcR beta is functional in terms of transmitting a signal for clonal deletion.
对一个T细胞受体(TcR)β链基因转基因小鼠(TGM)品系中内源性TcRβ链的表达进行了检测。与报道的许多其他TGM品系不同,来自我们TGM品系的胸腺、脾脏以及器官培养的胎儿胸腺中的相当一部分T细胞在其表面表达内源性TCRβ链。与此相符的是,通过聚合酶链反应(PCR)阐明了内源性β链基因的VDJ重排。胸腺细胞亚群的三色流式细胞术分析表明,内源性和转基因TcRβ基因的表达水平以成熟阶段特异性方式受到调控。脾脏T细胞中内源性TcRβ阳性细胞的百分比比胸腺细胞高几倍,这表明TcR在T细胞外周化过程中发挥作用。携带次要淋巴细胞刺激(Mls)-la抗原的TGM中Vβ6阳性细胞被删除,这表明内源性TcRβ在传递克隆删除信号方面是有功能的。