Wilson R E, Hoey B, Margison G P
Cancer Research Campaign Department of Carcinogenesis, Paterson Institute for Cancer Research, Christie Hospital NHS Trust, Manchester, UK.
Carcinogenesis. 1993 Apr;14(4):679-83. doi: 10.1093/carcin/14.4.679.
The effect of exposure to whole-body gamma-irradiation or fast electrons on O6-alkylguanine-DNA-alkyltransferase (ATase) activity and mRNA abundance has been examined in mice. In response to gamma-radiation, hepatic ATase activity was significantly raised in BDF1 mice 24 h post-irradiation, reaching a maximum of 2- to 3-fold at 36 h and beginning to decrease by 48-60 h. A small but consistently higher level of induction was achieved when mice were exposed using a low dose rate (0.015 Gy/min) compared to a high dose rate (0.5 Gy/min). ATase activity was also induced approximately 2-fold 48 h post-irradiation in brain, kidney, lung and spleen, with a greater induction again observed in response to the lower dose rate. In response to fast electrons from a linear accelerator hepatic ATase activity was also induced 2- to 3-fold 48 h post-irradiation in BDF1, BALB/c, C57Bl and DBA2 strains. Induction of ATase activity in livers of BDF1 mice was observed 48 h after a total single dose of 5 Gy gamma-radiation (2-fold), increasing to a slightly higher level at 15 Gy, but no induction was observed at doses of 2 Gy and below. Although a maximum 2- to 3-fold induction of ATase activity was observed, mRNA levels were induced 3- to 4-fold by 48 h after a dose of 15 Gy. Furthermore, significant increases in mRNA levels were detected at low doses (1-2 Gy) at which there was no apparent increase in ATase activity. This suggests that ionizing radiation increases ATase levels by a process involving transcriptional upregulation but that strong post-transcriptional and/or translational controls operate to limit induction of enzyme activity to 2- to 3-fold. This is the first report of an in vivo induction of ATase by ionizing radiation in a species other than the rat.
在小鼠中研究了全身γ射线照射或快速电子照射对O6-烷基鸟嘌呤-DNA烷基转移酶(ATase)活性和mRNA丰度的影响。对于γ辐射,BDF1小鼠在照射后24小时肝脏ATase活性显著升高,在36小时达到最大值,为对照的2至3倍,48至60小时开始下降。与高剂量率(0.5 Gy/分钟)相比,低剂量率(0.015 Gy/分钟)照射小鼠时,诱导水平虽小但始终较高。照射后48小时,脑、肾、肺和脾中的ATase活性也诱导约2倍,低剂量率照射时诱导程度更高。对于来自直线加速器的快速电子,BDF1、BALB/c、C57Bl和DBA2品系小鼠在照射后48小时肝脏ATase活性也诱导2至3倍。BDF1小鼠单次总剂量5 Gyγ辐射后48小时观察到肝脏ATase活性诱导(2倍),15 Gy时诱导水平略高,但2 Gy及以下剂量未观察到诱导。虽然观察到ATase活性最大诱导2至3倍,但15 Gy剂量照射48小时后mRNA水平诱导3至4倍。此外,在低剂量(1至2 Gy)时检测到mRNA水平显著增加,此时ATase活性无明显增加。这表明电离辐射通过转录上调过程增加ATase水平,但强大的转录后和/或翻译控制将酶活性诱导限制在2至3倍。这是除大鼠外首次关于电离辐射在体内诱导ATase的报道。