Tsujimura K, Takahashi T, Morita A, Hasegawa-Nishiwaki H, Iwase S, Obata Y
Laboratory of Immunology, Aichi Cancer Center Research Institute, Nagoya, Japan.
J Exp Med. 1996 Dec 1;184(6):2175-84. doi: 10.1084/jem.184.6.2175.
To elucidate the funciton of the mouse TL antigen in the thymus, we have derived two TL transgenic mouse strains by introducing Tl alpha 2-3 of A strain origin with its own promoter onto a C3H background with no expression of TL in the thymus. These transgenic mouse strains, both of which express high levels of Tla2-3-TL antigen in their thymus, were analyzed for their T cell function with emphasis on cytotoxic T lymphocyte (CTL) generation. A T cell response against TL was induced in Tg. Tla2-3-1, Tg. Tla2-3-2, and control C3H mice by skin grafts from H-2Kb/T3b transgenic mice, Tg.Con.3-1, expressing T3b-TL ubiquitously. Spleen cells from mice that had rejected the T3b-TL positive skin grafts were restimulated in vitro with Tg. Con.3-1 irradiated spleen cells. In mixed lymphocyte cultures (MLC), approximately 20% and 15% of Thy-1+ T cells derived from Tg.Tla2-3-1 and Tg.Tla2-3-2, respectively, expressed TCR gamma delta, whereas almost all those from C3H expressed TCR alpha beta. The MLC from Tg. Tla2-3-2 and C3H demonstrated high CTL activity against TL, while those from Tg. Tla2-3-1 had little or none. The generation of gamma delta CTL recognizing TL in Tg. Tla2-3-2, but not C3H mice, was confirmed by the establishment of CTL clones. A total of 14 gamma delta CTL clones were established from Tg. Tla2-3-2, whereas none were obtained from C3H. Of the 14 gamma delta CTL clones, 8 were CD8+ and 6 were CD4-CD8- double negative. The CTL activity of all these clones was TL specific and inhibited by anti-TL, but not by anti-H-2 antibodies, demonstrating that they recognize TL directly without antigen presentation by H-2. The CTL activity was blocked by antibodies to TCR gamma delta and CD3, and also by antibodies to CD 8 alpha and CD8 beta in CD8+ clones, showing that the activity was mediated by TCR gamma delta and coreceptors. The thymic origin of these gamma delta CTL clones was indicated by the expression of Thy-1 and Ly-1 (CD5), and also CD8 alpha beta heterodimers in CD8+ clones on their surfaces and by the usage of TCR V gamma 4 chains in 12 of the 14 clones. Taken together, these results suggest that Tla2-3-TL antigen expressed in the thymus engages in positive selection of a sizable population of gamma delta T cells.
为阐明小鼠TL抗原在胸腺中的功能,我们通过将A品系来源的Tlα2 - 3及其自身启动子导入胸腺中不表达TL的C3H背景,获得了两个TL转基因小鼠品系。这两个转基因小鼠品系在胸腺中均表达高水平的Tla2 - 3 - TL抗原,我们对其T细胞功能进行了分析,重点是细胞毒性T淋巴细胞(CTL)的产生。通过来自普遍表达T3b - TL的H - 2Kb/T3b转基因小鼠Tg.Con.3 - 1的皮肤移植,在Tg.Tla2 - 3 - 1、Tg.Tla2 - 3 - 2和对照C3H小鼠中诱导了针对TL的T细胞应答。将已排斥T3b - TL阳性皮肤移植的小鼠的脾细胞与经照射的Tg.Con.3 - 1脾细胞在体外进行再刺激。在混合淋巴细胞培养(MLC)中,分别来自Tg.Tla2 - 3 - 1和Tg.Tla2 - 3 - 2的Thy - 1 + T细胞中约20%和15%表达TCRγδ,而几乎所有来自C3H的Thy - 1 + T细胞表达TCRαβ。来自Tg.Tla2 - 3 - 2和C3H的MLC对TL表现出高CTL活性,而来自Tg.Tla2 - 3 - 1的MLC几乎没有或没有CTL活性。通过建立CTL克隆证实了在Tg.Tla2 - 3 - 2而非C3H小鼠中产生了识别TL的γδCTL。从Tg.Tla2 - 3 - 2中总共建立了14个γδCTL克隆,而从C3H中未获得任何克隆。在这14个γδCTL克隆中,8个是CD8 + ,6个是CD4 - CD8 - 双阴性。所有这些克隆的CTL活性都是TL特异性的,并且被抗TL抗体抑制,但不被抗H - 2抗体抑制,表明它们直接识别TL而无需H - 2进行抗原呈递。CTL活性被抗TCRγδ和CD3抗体阻断,在CD8 + 克隆中也被抗CD8α和CD8β抗体阻断,表明该活性是由TCRγδ和共受体介导的。这些γδCTL克隆的胸腺起源通过其表面Thy - 1和Ly - 1(CD5)的表达以及CD8 + 克隆中CD8αβ异二聚体的表达以及14个克隆中的12个使用TCR Vγ4链来表明。综上所述,这些结果表明胸腺中表达的Tla2 - 3 - TL抗原参与了相当数量的γδT细胞的阳性选择。