Kojima H, Shinohara N, Hanaoka S, Someya-Shirota Y, Takagaki Y, Ohno H, Saito T, Katayama T, Yagita H, Okumura K
Laboratory of Cellular Immunology, Mitsubishi Kasei Institute of Life Sciences, Tokyo, Japan.
Immunity. 1994 Aug;1(5):357-64. doi: 10.1016/1074-7613(94)90066-3.
To study the contribution of putative perforin-independent mechanism in the antigen-specific target destruction by cytotoxic T lymphocytes CD8+ CTL lines were established from spleen cells of chimeric mice produced by injecting perforin (-/-) embryonic stem cells into blastocysts of RAG-2(-/-) mice. When tested on normal concanavalin A blasts, these perforin-deficient cytotoxic T lymphocyte lines were found to be capable of inducing antigen-specific target cell lysis accompanied by DNA degradation. In contrast, with target cells carrying a mutation in Fas molecule, perforin-independent cytotoxicity was not detectable. These data not only confirmed the primary role of perforin but simultaneously revealed a major contribution of a perforin-independent Fas-mediated pathway in antigen-specific cytolysis.
为研究推定的不依赖穿孔素的机制在细胞毒性T淋巴细胞(CD8⁺CTL)进行抗原特异性靶细胞破坏中的作用,通过将穿孔素(-/-)胚胎干细胞注射到RAG-2(-/-)小鼠的囊胚中产生嵌合小鼠,从其脾细胞建立了CTL系。当在正常伴刀豆球蛋白A刺激的细胞上进行测试时,发现这些缺乏穿孔素的细胞毒性T淋巴细胞系能够诱导抗原特异性靶细胞裂解并伴有DNA降解。相反,对于Fas分子发生突变的靶细胞,未检测到不依赖穿孔素的细胞毒性。这些数据不仅证实了穿孔素的主要作用,同时还揭示了不依赖穿孔素的Fas介导途径在抗原特异性细胞溶解中的主要作用。