Kaneda R, Kasai M, Itoh Y, Iwabuchi K, Onoé K
Section of Pathology, Hokkaido University, Japan.
Microbiol Immunol. 1997;41(1):51-61. doi: 10.1111/j.1348-0421.1997.tb01172.x.
The selective induction of effector functions of a T-cell clone (DB14), specific to pigeon cytochrome c 43-58 (p 43-58) and restricted to I-Ab, was analyzed using a professional antigen-presenting cell, B hybridoma (Th 2.58), and various non-professional antigen-presenting cells (APC), L cells transfected with I-Ab (I-Ab L cells), a medullary thymic epithelial cell line (m-TEC) and a cortical thymic epithelial cell line (c-TEC). The m-TEC, and c-TEC expressed I-Ab upon induction with interferon gamma (IFN-gamma). When stimulated with p 43-58 in the presence of I-Ab L cells as well as Th 2.58 cells, the DB14 cells showed marked proliferation and, after 18 hr of culturing, exhibited significant cytotoxicity against the APC. By contrast, in the presence of m, c-TEC, the DB14 cells showed neither proliferation nor cytotoxicity against these TEC but exhibited considerable detachment activity towards them. Furthermore, DB14 cells became expressed activation markers CD69 or CD44) following stimulation with p 43-58 plus m-TEC or c-TEC. The addition of rIL-2 to the culture of DC14 cells, p 43-58 and m-TEC or c-TEC, restored the proliferative responses. However, it was shown that anergy was not involved in the negligible proliferative responses of DB14 cells after stimulation with p 43-58 plus m, c-TEC. The present findings indicate that differences in APC functions are present among the non-professional APC and suggest that the selective induction of T-cell functions can be achieved using the appropriate non-professional APC. The characteristic activation of T cells by TEC may be related to their functional roles in situ.
利用专业抗原呈递细胞B杂交瘤(Th 2.58)以及各种非专业抗原呈递细胞(APC),即转染了I-Ab的L细胞(I-Ab L细胞)、髓质胸腺上皮细胞系(m-TEC)和皮质胸腺上皮细胞系(c-TEC),分析了对鸽细胞色素c 43-58(p 43-58)特异且受限于I-Ab的T细胞克隆(DB14)效应功能的选择性诱导。m-TEC和c-TEC在γ干扰素(IFN-γ)诱导下表达I-Ab。当在I-Ab L细胞以及Th 2.58细胞存在的情况下用p 43-58刺激时,DB14细胞显示出明显的增殖,并且在培养18小时后,对APC表现出显著的细胞毒性。相比之下,在m-TEC和c-TEC存在的情况下,DB14细胞既不增殖,也不对这些TEC表现出细胞毒性,但对它们表现出相当大的脱离活性。此外,在用p 43-58加m-TEC或c-TEC刺激后,DB14细胞表达了活化标志物CD69或CD44。向DC14细胞、p 43-58和m-TEC或c-TEC的培养物中添加重组白细胞介素-2(rIL-2)可恢复增殖反应。然而,结果表明,在用p 43-58加m-TEC和c-TEC刺激后DB14细胞可忽略不计的增殖反应中,无反应性并不涉及其中。目前的研究结果表明,非专业APC之间存在APC功能差异,并表明使用合适的非专业APC可以实现T细胞功能的选择性诱导。TEC对T细胞的特征性活化可能与其在原位的功能作用有关。