Allbritton N L, Nagler-Anderson C, Elliott T J, Verret C R, Eisen H N
Department of Biology, Massachusetts Institute of Technology, Cambridge 02139.
J Immunol. 1988 Nov 15;141(10):3243-8.
When mouse target cells are subjected to cytolytic attack by mouse CTL cell lines that have been cultured for many months in high levels of IL-2, and have abundant perforin-rich secretory granules, they exhibit two prominent changes: 1) rapid and massive increase (greater than 10-fold) in intracellular Ca2+ concentration and 2) fragmentation of DNA into nucleosome-sized fragments. We show here that when the same target cells are subjected to cytolytic attack by perforin-deficient CTL, either human CTL or primary mouse CTL from peritoneal exudates, the same changes are observed, suggesting that perforin-rich and perforin-deficient CTL kill their target cells by similar (if not identical) mechanisms. It is possible that perforin-deficient CTL produce enough perforin to destroy target cells but not enough to be detected by currently available methods.
当小鼠靶细胞受到在高水平白细胞介素-2中培养了数月且具有丰富的富含穿孔素的分泌颗粒的小鼠细胞毒性T淋巴细胞(CTL)细胞系的溶细胞攻击时,它们会出现两个显著变化:1)细胞内钙离子浓度迅速大幅增加(超过10倍);2)DNA断裂成核小体大小的片段。我们在此表明,当相同的靶细胞受到穿孔素缺陷型CTL(人CTL或来自腹膜渗出液的原代小鼠CTL)的溶细胞攻击时,会观察到相同的变化,这表明富含穿孔素的CTL和穿孔素缺陷型CTL通过相似(即便不是相同)的机制杀死它们的靶细胞。有可能穿孔素缺陷型CTL产生了足够的穿孔素来破坏靶细胞,但不足以被目前可用的方法检测到。