Ucker D S
Nature. 1987;327(6117):62-4. doi: 10.1038/327062a0.
Cytotoxic T lymphocytes (CTL) induce a cytolytic process in target cells which, like the glucocorticoid-mediated cytolysis of immature thymocytes, effects a rapid and characteristic degradation of chromosomal DNA. I have explored the possibility that these two lethal processes share a common pathway by studying the susceptibility of glucocorticoid-resistant mutants to CTL-mediated killing. Here, I report that an unusual thymoma mutant, which has normal hormone receptor activity, is resistant to both glucocorticoids and CTL. The failure to be killed by CTL is not due to an inability of this 'deathless' mutant to be recognized. Further, a single-step reversion can restore sensitivity to both glucocorticoids and CTL. The genetic locus thus identified may reveal one element of an endogenous suicide pathway that can be triggered by different effectors. Unlike complement-mediated lysis, the processes of glucocorticoid- and CTL-mediated cytolysis seem to require that target cells be active in their own death.
细胞毒性T淋巴细胞(CTL)在靶细胞中诱导一种溶细胞过程,这种过程类似于糖皮质激素介导的未成熟胸腺细胞的溶细胞作用,会导致染色体DNA迅速且有特征性的降解。我通过研究糖皮质激素抗性突变体对CTL介导杀伤的敏感性,探讨了这两种致死过程是否共享一条共同途径的可能性。在此,我报告一种不寻常的胸腺瘤突变体,其具有正常的激素受体活性,对糖皮质激素和CTL均具有抗性。不能被CTL杀死并非由于这种“不死”突变体无法被识别。此外,一步回复突变可恢复对糖皮质激素和CTL的敏感性。由此确定的基因位点可能揭示了一种可被不同效应器触发的内源性自杀途径的一个要素。与补体介导的溶解不同,糖皮质激素和CTL介导的溶细胞过程似乎要求靶细胞在自身死亡过程中处于活跃状态。