Sasahara T, Tamauchi H, Ikewaki N, Kubota K
Department of Microbiology, Kitasato University School of Medicine, Kanagawa, Japan.
Microbiol Immunol. 1994;38(3):191-9. doi: 10.1111/j.1348-0421.1994.tb01764.x.
Growth factor-dependent gut intraepithelial lymphocyte (IEL) cell lines were established from a long-term in vitro culture of BALB/c IEL with syngeneic irradiated spleen cells in the presence of concanavalin A-stimulated spleen supernatant fluids. The cell lines were preferentially consisted of very limited thymoindependent subsets of IEL; i.e., Thy-1+CD5-TCR alpha beta+CD4+CD8 alpha+beta- (double-positive; DP) IEL and Thy-1+CD5-TCR alpha beta+CD4-CD8 alpha+beta- (CD8 single-positive; CD8 SP) IEL. The CD8 SP IEL cell line had cytotoxic activities and was triggered to proliferate by T-cell receptor (TCR)-directed stimuli. The DP IEL cell line expressed high levels of the CD3-TCR alpha beta, exhibited cytotoxic activity in redirected lysis assays, and had perforin in the cytoplasm, indicating the functional maturity of this cell line. However, the DP IEL cell line did not proliferate in response to TCR alpha beta-directed stimuli, which indicated that TCR alpha beta-mediated signalling was able to initiate cytotoxic function but not to induce proliferation of the DP IEL cell line. Although both cell lines were shown to have functional competence, they expressed J11d antigen which marks immaturity in thymocyte differentiation pathways. These results indicate that the established thymoindependent DP and CD8 SP IEL cell lines have unique properties distinct from DP thymocytes and CD8 SP peripheral T cells. Together with a recent report on freshly isolated DP IEL (10), the unique properties of the DP IEL cell line seems to support the notion that DP IEL may undergo a unique maturation process in the gut microenvironment.
通过在伴刀豆球蛋白A刺激的脾上清液存在的情况下,将BALB/c肠上皮内淋巴细胞(IEL)与同基因照射的脾细胞进行长期体外培养,建立了生长因子依赖性IEL细胞系。这些细胞系优先由非常有限的胸腺非依赖性IEL亚群组成;即,Thy-1+CD5-TCRαβ+CD4+CD8α+β-(双阳性;DP)IEL和Thy-1+CD5-TCRαβ+CD4-CD8α+β-(CD8单阳性;CD8 SP)IEL。CD8 SP IEL细胞系具有细胞毒活性,并被T细胞受体(TCR)导向的刺激触发增殖。DP IEL细胞系高水平表达CD3-TCRαβ,在重定向裂解试验中表现出细胞毒活性,并且细胞质中有穿孔素,表明该细胞系功能成熟。然而,DP IEL细胞系对TCRαβ导向的刺激无增殖反应,这表明TCRαβ介导的信号传导能够启动细胞毒功能,但不能诱导DP IEL细胞系增殖。尽管两个细胞系都显示具有功能活性,但它们表达J11d抗原,该抗原标志着胸腺细胞分化途径中的不成熟。这些结果表明,建立的胸腺非依赖性DP和CD8 SP IEL细胞系具有与DP胸腺细胞和CD8 SP外周T细胞不同的独特特性。连同最近关于新鲜分离的DP IEL的报告(10),DP IEL细胞系的独特特性似乎支持DP IEL可能在肠道微环境中经历独特成熟过程的观点。