Sassa Akira, Fukuda Takayuki, Ukai Akiko, Nakamura Maki, Takabe Michihito, Takamura-Enya Takeji, Honma Masamitsu, Yasui Manabu
1Department of Biology, Graduate School of Science, Chiba University, Chiba, 263-8522 Japan.
2Tokyo Laboratory, BoZo Research Center Inc, 1-3-11, Hanegi, Setagaya-ku, Tokyo, 156-0042 Japan.
Genes Environ. 2019 Jul 16;41:15. doi: 10.1186/s41021-019-0130-y. eCollection 2019.
The human genome is constantly exposed to numerous environmental genotoxicants. To prevent the detrimental consequences induced by the expansion of damaged cells, cellular protective systems such as nucleotide excision repair (NER) exist and serve as a primary pathway for repairing the various helix-distorting DNA adducts induced by genotoxic agents. NER is further divided into two sub-pathways, namely, global genomic NER (GG-NER) and transcription-coupled NER (TC-NER). Both NER sub-pathways are reportedly involved in the damage response elicited by exposure to genotoxins. However, how disruption of these sub-pathways impacts the toxicity of different types of environmental mutagens in human cells is not well understood.
To evaluate the role of NER sub-pathways on the cytotoxic effects of mutagens, we disrupted and to selectively inactivate GG-NER and TC-NER, respectively, in human lymphoblastoid TK6 cells, a standard cell line used in genotoxicity studies. Using these cells, we then comparatively assessed their respective sensitivities to representative genotoxic agents, including ultraviolet C (UVC) light, benzo [a] pyrene (B(a)P), 2-amino-3,8-dimethylimidazo [4,5-f] quinoxaline (MeIQx), 2-amino-1-methyl-6-phenylimidazo [4,5-b] pyridine (PhIP), γ-ray, and 2-acetylaminofluorene (2-AAF). cells exhibited a hyper-sensitivity to UVC, B(a)P, and MeIQx. On the other hand, cells were highly sensitive to UVC, but not to B(a)P and MeIQx, compared with wild-type cells. In contrast with other genotoxins, the sensitivity of cells against PhIP was significantly higher than cells. The toxicity of γ-ray and 2-AAF was not enhanced by disruption of either or in the cells.
Based on our findings, genetically modified TK6 cells appear to be a useful tool for elucidating the detailed roles of the various repair factors that exist to combat genotoxic agents, and should contribute to the improved risk assessment of environmental chemical contaminants.
人类基因组不断暴露于众多环境基因毒性物质中。为防止受损细胞扩增所引发的有害后果,细胞保护系统如核苷酸切除修复(NER)得以存在,并作为修复由基因毒性剂诱导产生的各种螺旋扭曲DNA加合物的主要途径。NER进一步分为两个子途径,即全局基因组NER(GG-NER)和转录偶联NER(TC-NER)。据报道,这两个NER子途径均参与了因接触基因毒素而引发的损伤反应。然而,这些子途径的破坏如何影响人类细胞中不同类型环境诱变剂的毒性,目前尚不清楚。
为评估NER子途径对诱变剂细胞毒性作用的影响,我们分别破坏 和 ,以选择性地使人类淋巴母细胞TK6细胞(遗传毒性研究中使用的标准细胞系)中的GG-NER和TC-NER失活。然后,利用这些细胞,我们比较评估了它们对代表性基因毒性剂的各自敏感性,这些基因毒性剂包括紫外线C(UVC)光、苯并[a]芘(B(a)P)、2-氨基-3,8-二甲基咪唑[4,5-f]喹喔啉(MeIQx)、2-氨基-1-甲基-6-苯基咪唑[4,5-b]吡啶(PhIP)、γ射线和2-乙酰氨基芴(2-AAF)。 细胞对UVC、B(a)P和MeIQx表现出超敏感性。另一方面,与野生型细胞相比, 细胞对UVC高度敏感,但对B(a)P和MeIQx不敏感。与其他基因毒素不同, 细胞对PhIP的敏感性显著高于 细胞。细胞中 或 的破坏并未增强γ射线和2-AAF的毒性。
基于我们的研究结果,基因改造的TK6细胞似乎是阐明对抗基因毒性剂的各种修复因子详细作用的有用工具,并且应该有助于改进对环境化学污染物的风险评估。