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纳米材料诱导 DNA-蛋白质交联和 DNA 氧化:使用 RTG-2 鱼类细胞系和彗星试验改良进行的机制研究。

Nanomaterials induce DNA-protein crosslink and DNA oxidation: A mechanistic study with RTG-2 fish cell line and Comet assay modifications.

机构信息

Genetics Department, Federal University of Paraná, Curitiba, Paraná State, Brazil.

Chemistry Department, State University of Ponta Grossa, Ponta Grossa, Paraná State, Brazil.

出版信息

Chemosphere. 2019 Jan;215:703-709. doi: 10.1016/j.chemosphere.2018.10.118. Epub 2018 Oct 17.


DOI:10.1016/j.chemosphere.2018.10.118
PMID:30347365
Abstract

Genotoxic effects of nanomaterials (NMs) have been controversially reported in literature, and the mode of action (MoA) via DNA oxidation is cited as the main damage caused by them. Evidence of nano-silver as a crosslinker has been previously reported by the present research team in an in vivo fish genotoxicity study. Thus, aiming to confirm the evidence about NMs as crosslinker agent, the present investigation elucidated the genotoxic potential of NMs and their genotoxic MoA through in vitro assay with RTG-2 cells line (rainbow trout gonadal) by exposure to nano-silver (PVP-coated) and nano-titanium. The types and levels of DNA damage were assessed by the Comet assay (standard alkaline, hOGG1-modified alkaline, and two crosslink-modified alkaline versions). It was demonstrated that the use of the standard alkaline Comet assay alone may inaccurately predict the genotoxicity of NMs since oxidative and crosslink DNA damages were also verified in RTG-2 cells when assessed by the modified versions of the alkaline protocol. More importantly, it was confirmed that both nano-silver and nano-titanium acted as DNA-protein crosslinkers through the Comet assay version with proteinase K. As both nano-silver and nano-titanium present a great risk to aquatic life, these findings reinforce the need of genotoxicity testing strategies that encompass the assessment of different types of DNA damage, in order to ensure an accurate prediction of the genotoxic potential of NMs.

摘要

纳米材料(NMs)的遗传毒性效应在文献中存在争议,其通过氧化 DNA 导致损伤的作用模式(MoA)被认为是主要的损伤机制。本研究团队之前在一项体内鱼类遗传毒性研究中已经报道了纳米银作为交联剂的证据。因此,为了证实纳米材料作为交联剂的证据,本研究通过 RTG-2 细胞系(虹鳟性腺)的体外试验,阐明了纳米银(PVP 包覆)和纳米钛的遗传毒性潜力及其遗传毒性 MoA。通过彗星试验(标准碱性、hOGG1 改良碱性和两种交联改良碱性版本)评估了 DNA 损伤的类型和水平。结果表明,仅使用标准碱性彗星试验可能无法准确预测纳米材料的遗传毒性,因为当使用碱性试验的改良版本评估时,RTG-2 细胞中也检测到了氧化和交联 DNA 损伤。更重要的是,通过带有蛋白酶 K 的彗星试验版本证实了纳米银和纳米钛均作为 DNA-蛋白质交联剂。由于纳米银和纳米钛都对水生生物有很大的风险,这些发现强调了需要采用遗传毒性测试策略来评估不同类型的 DNA 损伤,以确保对纳米材料的遗传毒性潜力进行准确预测。

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