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全氟辛烷磺酸在 gptDelta 转基因系统中的诱变效应是由过氧化氢介导的。

Mutagenic Effects of Perfluorooctanesulfonic Acid in gpt Delta Transgenic System Are Mediated by Hydrogen Peroxide.

机构信息

†Key Laboratory of Ion Beam Bioengineering, Hefei Institutes of Physical Science, Chinese Academy of Sciences and Anhui Province, Hefei, Anhui 230031, P. R. China.

‡Jiangsu Tripod Preclinical Research Laboratories, Pukou Economic Development Zone, 9# Xinglong Road, Nanjing, China.

出版信息

Environ Sci Technol. 2015 May 19;49(10):6294-303. doi: 10.1021/acs.est.5b00530. Epub 2015 Apr 30.

Abstract

Perfluorooctane sulfate (PFOS), a persistent organic pollutant, has recently been closely linked with an increased risk of tumorigenesis. However, PFOS has yielded negative results in various tests of genotoxicity. The present study aimed to investigate the mutagenic response to PFOS in the gpt delta transgenic mouse mutation system and to illustrate the contribution of hydrogen peroxide (H2O2) to PFOS genotoxicity. Mutations at the redBA/gam loci were determined by Spi(-) assay both in vitro and in vivo. DNA damage was measured by phosphorylated histone H2AX (γ-H2AX) and mouse bone marrow micronucleus (MN) testing. Our data showed that PFOS induced concentration-dependent increases in γ-H2AX foci and in mutation frequencies at redBA/gam loci in transgenic mouse embryonic fibroblast cells, which were confirmed by the formation of MNs in the bone marrow and the observations of mutation induction in the livers of gpt delta transgenic mice. Concurrent treatment with catalase, an efficient H2O2 scavenger, significantly decreased the formation of γ-H2AX foci and the mutation yields induced by PFOS. In addition, the generation of H2O2 was found to be closely related to the abnormal peroxisomal β-oxidation caused by PFOS. These finding might provide new mechanistical information about genotoxic effects of PFOS.

摘要

全氟辛烷磺酸(PFOS)作为一种持久性有机污染物,最近与肿瘤形成风险增加密切相关。然而,PFOS 在各种遗传毒性测试中均呈阴性结果。本研究旨在探讨 PFOS 在 gpt delta 转基因鼠突变系统中的致突变反应,并阐明过氧化氢(H2O2)对 PFOS 遗传毒性的贡献。通过 Spi(-)试验在体外和体内检测 redBA/gam 基因座的突变。通过磷酸化组蛋白 H2AX(γ-H2AX)和小鼠骨髓微核(MN)试验测量 DNA 损伤。我们的数据表明,PFOS 诱导了转基因小鼠胚胎成纤维细胞中 γ-H2AX 焦点和 redBA/gam 基因座突变频率的浓度依赖性增加,这在骨髓中的 MN 形成和 gpt delta 转基因小鼠肝脏中的突变诱导观察中得到了证实。同时用过氧化氢酶(一种有效的 H2O2 清除剂)处理可显著降低 PFOS 诱导的 γ-H2AX 焦点形成和突变产量。此外,还发现 H2O2 的生成与 PFOS 引起的异常过氧化物酶体 β-氧化密切相关。这些发现可能为 PFOS 的遗传毒性作用提供新的机制信息。

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