Takahashi A
Department of Biology, Nara Medical University, Kashihara, Japan.
Int J Radiat Biol. 2001 Feb;77(2):215-24. doi: 10.1080/09553000010009495.
This study was undertaken to clarify the effects of acute or chronic pre-irradiation on the induction of p53-dependent apoptosis by X-rays or heat shock.
Having an identical genotype except for p53-status, the human cultured squamous cell carcinoma cells (SAS) were transfected with a mutant p53 gene (SAS/mp53) or neo alone (SAS/neo) as a control. After acute X-irradiation (1 Gy min(-1)), chronic gamma-irradiation (0.001 Gy min(-1)) or heat shock (44 degrees C), the cells were for the incidence of apoptotic bodies and DNA ladders, cellular levels of p53 and bax, and caspase-3 activity.
It was found that (1) a challenge treatment with X-rays (5.O Gy) or heat shock (30 min) immediately after chronic pre-irradiation (1.5 Gy) but not acute pre-irradiation (1.5 Gy) resulted in lower levels of apoptosis than those observed after challenge treatment only in SAS/neo cells; (2) a challenge treatment-induced apoptosis was observed 48 h after cessation of chronic pre-irradiation in SAS/neo cells; (3) apoptosis was barely increased in SAS/mp53 cells; and (4) the levels of apoptosis-related proteins after challenge treatments were strongly correlated with the above phenomena.
Chronic pre-irradiation at a low dose-rate suppressed induction of p53-dependent apoptosis via bax and caspase-3. These findings suggest that chronic pre-irradiation suppressed p53 function through radiation-induced signalling and/or p53 stability.
本研究旨在阐明急性或慢性预照射对X射线或热休克诱导的p53依赖性细胞凋亡的影响。
除p53状态外具有相同基因型的人培养鳞状细胞癌(SAS)细胞,用突变型p53基因(SAS/mp53)或单独的neo(SAS/neo)作为对照进行转染。在急性X射线照射(1 Gy min⁻¹)、慢性γ射线照射(0.001 Gy min⁻¹)或热休克(44℃)后,检测细胞凋亡小体和DNA梯带的发生率、p53和bax的细胞水平以及caspase-3活性。
发现(1)在慢性预照射(1.5 Gy)后立即用X射线(5.0 Gy)或热休克(30分钟)进行激发处理,但急性预照射(1.5 Gy)后则未出现这种情况,与仅在SAS/neo细胞中进行激发处理后相比,导致凋亡水平降低;(2)在SAS/neo细胞中,慢性预照射停止后48小时观察到激发处理诱导的细胞凋亡;(3)SAS/mp53细胞中的凋亡几乎没有增加;(4)激发处理后凋亡相关蛋白的水平与上述现象密切相关。
低剂量率的慢性预照射通过bax和caspase-3抑制p53依赖性细胞凋亡的诱导。这些发现表明,慢性预照射通过辐射诱导的信号传导和/或p53稳定性抑制p53功能。