Sun X M, Snowden R T, Dinsdale D, Ormerod M G, Cohen G M
MRC Toxicology Unit, Centre for Mechanisms of Human Toxicity, University of Leicester, U.K.
Biochem Pharmacol. 1994 Jan 20;47(2):187-95. doi: 10.1016/0006-2952(94)90005-1.
Etoposide, a DNA topoisomerase II inhibitor, caused a concentration-dependent induction of apoptosis in immature thymocytes. Using a flow cytometric method to separate and quantify normal and apoptotic cells, etoposide-induced apoptosis was inhibited by cycloheximide and actinomycin D but not by zinc. Etoposide induced a marked cleavage of DNA into nucleosomal length fragments or multiples thereof, which was completely inhibited if the thymocytes were also incubated in the presence of zinc. Etoposide, alone, induced the classical ultrastructural features of apoptosis, but in the presence of zinc, the morphological pattern was markedly different and dominated by discrete clumps of condensed chromatin abutting the nuclear membrane. These latter changes resemble those described as the earliest changes in apoptosis. These results support the hypothesis that, in the induction of apoptosis, critical alterations in nuclear chromatin occur prior to endonuclease cleavage of DNA into nucleosomal fragments.
依托泊苷是一种DNA拓扑异构酶II抑制剂,可在未成熟胸腺细胞中引起浓度依赖性的细胞凋亡。使用流式细胞术方法分离和定量正常细胞和凋亡细胞,环己酰亚胺和放线菌素D可抑制依托泊苷诱导的细胞凋亡,但锌不能抑制。依托泊苷可诱导DNA显著切割成核小体长度的片段或其倍数,如果胸腺细胞也在锌存在的情况下孵育,则这种切割会被完全抑制。单独使用依托泊苷可诱导典型的细胞凋亡超微结构特征,但在锌存在的情况下,形态模式明显不同,主要表现为紧贴核膜的离散染色质凝聚块。后一种变化类似于被描述为细胞凋亡最早变化的那些变化。这些结果支持这样一种假说,即在细胞凋亡的诱导过程中,核染色质的关键改变发生在DNA被核酸内切酶切割成核小体片段之前。