Woloschak G E, Chang-Liu C M, Jones P S, Jones C A
Biological and Medical Research Division, Argonne National Laboratory, Illinois 60439-4833.
Cancer Res. 1990 Jan 15;50(2):339-44.
We examined the modulation of gene expression in Syrian hamster embryo (SHE) cells at various times following exposure to low doses of ionizing radiation. Early passage SHE cells were irradiated in plateau phase (greater than 95% G0-G1 cells) with 21-cGy fission-spectrum neutrons, 75-cGy X-rays, or 90-cGy gamma-rays, none of which induced more than 10% loss in cell viability. RNA harvested at various times after exposure was examined for levels of particular RNA species by dot blot and Northern blot hybridizations. Levels of beta-actin-specific RNA decreased within 15 min after exposure of the cells. The kinetics of repression of beta-actin mRNA were similar for all qualities of radiation (X-rays, gamma-rays, and neutrons) for 12 h post-irradiation. Within 1 h after neutron exposure (21 cGy), we observed a decrease in accumulation of RNA species (relative to RNA from nonirradiated cells) encoding the enzyme ornithine decarboxylase; this decrease continued for up to 12 h. Similar results were obtained with gamma- and X-rays. RNA encoding interleukin 1, however, was induced by 3 h after neutron irradiation but reduced to background levels by 7 h. Amounts of rRNA remained constant in all experiments, although total transcription on a per cell basis was reduced within 15 min following irradiation and did not return to normal until 7 h post-irradiation. No alterations, relative to untreated control cells, in overall cell viability or the rate of cell cycle progression were observed in cells either immediately or within 24 h post-irradiation. Our results demonstrate modulation of specific genes following low-dose irradiation. In addition, our findings suggest that some molecular responses to different qualities of ionizing radiation (X-rays, gamma-rays, and neutrons) may be similar.
我们研究了低剂量电离辐射照射后不同时间叙利亚仓鼠胚胎(SHE)细胞中基因表达的调节情况。将处于平台期(超过95%为G0 - G1期细胞)的早期传代SHE细胞用21厘戈瑞裂变谱中子、75厘戈瑞X射线或90厘戈瑞γ射线进行照射,这些辐射均未导致细胞活力损失超过10%。在照射后的不同时间收集RNA,通过斑点印迹和Northern印迹杂交检测特定RNA种类的水平。细胞暴露后15分钟内,β - 肌动蛋白特异性RNA水平下降。照射后12小时内,所有辐射类型(X射线、γ射线和中子)对β - 肌动蛋白mRNA的抑制动力学相似。中子照射(21厘戈瑞)后1小时内,我们观察到编码鸟氨酸脱羧酶的RNA种类(相对于未照射细胞的RNA)积累减少;这种减少持续长达12小时。γ射线和X射线照射也得到了类似结果。然而,编码白细胞介素1的RNA在中子照射后3小时被诱导,但在7小时时降至背景水平。在所有实验中,rRNA的量保持恒定,尽管照射后15分钟内每个细胞的总转录量减少,且直到照射后7小时才恢复正常。照射后立即或24小时内,相对于未处理的对照细胞,未观察到细胞总体活力或细胞周期进展速率有改变。我们的结果表明低剂量照射后特定基因发生了调节。此外,我们的发现表明,对不同类型电离辐射(X射线、γ射线和中子)的一些分子反应可能是相似的。