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Cells die with increased cytosolic ATP during apoptosis: a bioluminescence study with intracellular luciferase.

机译:细胞凋亡过程中细胞溶质ATP增加而死亡:一项使用细胞内萤光素酶的生物发光研究。

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Apoptosis is a distinct form of cell death, which requires energy. Here, we made real-time continuous measurements of the cytosolic ATP level throughout the apoptotic process in intact HeLa, PC12 and U937 cells transfected with the firefly luciferase gene. Apoptotic stimuli (staurosporine (STS), tumor necrosis factor alpha (TNFalpha), etoposide) induced significant elevation of the cytosolic ATP level. The cytosolic ATP level remained at a higher level than in the control for up to 6 h during which activation of caspase-3 and internucleosomal DNA fragmentation took place. When the STS-induced ATP response was abolished by glucose deprivation-induced inhibition of glycolysis, both caspase activation and DNA laddering were completely inhibited. Annexin V-binding induced by STS or TNFalpha was largely suppressed by glycolysis inhibition. Thus, it is suggested that the cells die with increased cytosolic ATP, and elevation of cytosolic ATP level is a requisite to the apoptotic cell death process.
机译:凋亡是细胞死亡的一种独特形式,需要能量。在这里,我们对整个萤火虫荧光素酶基因转染的完整HeLa,PC12和U937细胞凋亡过程中胞质ATP水平进行了实时连续测量。凋亡刺激(星形孢菌素(STS),肿瘤坏死因子α(TNFα),依托泊苷)引起细胞内ATP水平的显着升高。在长达6小时的时间内,胞质ATP的水平保持在比对照组更高的水平,在此过程中发生了caspase-3的激活和核小体间DNA片段化。当葡萄糖剥夺诱导的糖酵解抑制取消了STS诱导的ATP反应时,胱天蛋白酶激活和DNA梯形化都被完全抑制。 STS或TNFalpha诱导的膜联蛋白V结合在很大程度上被糖酵解抑制所抑制。因此,提示细胞以增加的胞质ATP死亡,胞质ATP水平升高是凋亡细胞死亡过程的必要条件。

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