Waterhouse Nigel J, Sutton Vivien R, Sedelies Karin A, Ciccone Annette, Jenkins Misty, Turner Stephen J, Bird Phillip I, Trapani Joseph A
Cancer Cell Death Laboratory, Cancer Immunology Program, Peter MacCallum Cancer Centre, Melbourne, Victoria 8006, Australia.
J Cell Biol. 2006 Apr 10;173(1):133-44. doi: 10.1083/jcb.200510072.
Cytotoxic T lymphocyte (CTL)-induced death triggered by the granule exocytosis pathway involves the perforin-dependent delivery of granzymes to the target cell. Gene targeting has shown that perforin is essential for this process; however, CTL deficient in the key granzymes A and B maintain the ability to kill their targets by granule exocytosis. It is not clear how granzyme AB(-/-) CTLs kill their targets, although it has been proposed that this occurs through perforin-induced lysis. We found that purified granzyme B or CTLs from wild-type mice induced classic apoptotic cell death. Perforin-induced lysis was far more rapid and involved the formation of large plasma membrane protrusions. Cell death induced by granzyme AB(-/-) CTLs shared similar kinetics and morphological characteristics to apoptosis but followed a distinct series of molecular events. Therefore, CTLs from granzyme AB(-/-) mice induce target cell death by a unique mechanism that is distinct from both perforin lysis and apoptosis.
由颗粒胞吐途径引发的细胞毒性T淋巴细胞(CTL)诱导的死亡涉及穿孔素依赖性地将颗粒酶递送至靶细胞。基因靶向研究表明,穿孔素对于这一过程至关重要;然而,缺乏关键颗粒酶A和B的CTL仍保持通过颗粒胞吐作用杀伤其靶标的能力。目前尚不清楚颗粒酶AB(-/-)CTL如何杀伤其靶标,尽管有人提出这是通过穿孔素诱导的细胞溶解发生的。我们发现,从野生型小鼠中纯化的颗粒酶B或CTL可诱导典型的凋亡性细胞死亡。穿孔素诱导的细胞溶解要快得多,且涉及大的质膜突起的形成。颗粒酶AB(-/-)CTL诱导的细胞死亡与凋亡具有相似的动力学和形态学特征,但遵循一系列不同的分子事件。因此,来自颗粒酶AB(-/-)小鼠的CTL通过一种独特的机制诱导靶细胞死亡,该机制不同于穿孔素介导的细胞溶解和凋亡。