Thielmann H W, Popanda O
German Cancer Research Center, Division of Interaction of Carcinogens with Biological Macromolecules, Im Neuenheimer Feld 280, Heidelberg, D-69120, Germany.
Int J Oncol. 1998 Feb;12(2):265-71. doi: 10.3892/ijo.12.2.265.
DNA topoisomerase II was monitored with the monoclonal antibody Ki-S1 in human fibroblasts after irradiation of cells with 254-nm UV light and -rays from a 137Cs source. DNA topoisomerase II was localized immunohistochemically as bright fluorescent dots in the karyoplasm. Investigated fibroblasts originated from normal human donors and a xeroderma pigmentosum patient (XP12BE). All cell lines showed a time and dose-dependent increase in DNA topoisomerase II abundance after irradiation. The increase may reflect enhanced accessibility of the enzyme, enhanced gene expression or enhanced stabilization of mRNA or protein molecules. The effect was detectable as early as 1 h after irradiation at doses 3 J/m2 or 3 Gy. It passed through a maximum and decreased within 18 h (UV light) or 6 h ( -rays). Except for the duration of the response, no principal differences were seen between the effects caused by UV light and those elicited by -rays. The increase in enzyme levels might be part of the well-known DNA damage responses which operate in cell-protective or DNA-reparative pathways or may reflect initiation of apoptosis. DNA topoisomerase I was detected with a commercially available polyclonal antibody raised against human DNA topoisomerase I. In unirradiated cells, DNA topoisomerase I was found to be mainly concentrated in nucleoli. Irradiation with -rays changed the staining pattern in that it caused a multitude of DNA topoisomerase I-rich centers to occur which may reflect sites of transcription of radiation-inducible genes.
在用254纳米紫外线和来自137铯源的γ射线照射人成纤维细胞后,用单克隆抗体Ki-S1监测DNA拓扑异构酶II。DNA拓扑异构酶II通过免疫组织化学定位为核质中明亮的荧光点。所研究的成纤维细胞来源于正常人类供体和一名着色性干皮病患者(XP12BE)。所有细胞系在照射后DNA拓扑异构酶II丰度均呈现时间和剂量依赖性增加。这种增加可能反映了该酶可及性增强、基因表达增强或mRNA或蛋白质分子稳定性增强。在剂量为3 J/m²或3 Gy时,照射后1小时即可检测到这种效应。它在18小时(紫外线)或6小时(γ射线)内达到最大值并下降。除了反应持续时间外,紫外线和γ射线所引起的效应未见主要差异。酶水平的增加可能是在细胞保护或DNA修复途径中起作用的著名DNA损伤反应的一部分,或者可能反映了细胞凋亡的启动。用针对人DNA拓扑异构酶I产生的市售多克隆抗体检测DNA拓扑异构酶I。在未照射的细胞中,发现DNA拓扑异构酶I主要集中在核仁中。γ射线照射改变了染色模式,导致出现大量富含DNA拓扑异构酶I的中心,这可能反映了辐射诱导基因的转录位点。