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接触 6-PPD 醌会导致铁死亡激活,从而引起秀丽隐杆线虫生殖毒性。

Exposure to 6-PPD quinone causes ferroptosis activation associated with induction of reproductive toxicity in Caenorhabditis elegans.

机构信息

Key Laboratory of Environmental Medicine Engineering of Ministry of Education, Medical School, Southeast University, Nanjing, China.

Jiangsu Provincial Center for Disease Control and Prevention, Nanjing, China.

出版信息

J Hazard Mater. 2024 Jun 5;471:134356. doi: 10.1016/j.jhazmat.2024.134356. Epub 2024 Apr 19.

Abstract

Exposure to N-(1,3-dimethylbutyl)-N'-phenyl-p-phenylenediamine quinone (6-PPDQ) caused toxicity on Caenorhabditis elegans, including reproductive toxicity. However, the underlying mechanisms for this induced reproductive toxicity by 6-PPDQ remain largely unclear. We examined possible association of ferroptosis activation with reproductive toxicity of 6-PPDQ. In 1-100 μg/L 6-PPDQ exposed nematodes, Fe content was increased, which was accompanied with enhanced lipid peroxidation, increased malonydialdehyde (MDA) content, and decreased L-glutathione (GSH) content. Exposure to 1-100 μg/L 6-PPDQ decreased expressions of ftn-1 encoding ferritin, ads-1 encoding AGPS, and gpx-6 encoding GPX4 and increased expression of bli-3 encoding dual oxidase. After 6-PPDQ exposure, RNAi of ftn-1 decreased ads-1 and gpx-6 expressions and increased bli-3 expression. RNAi of ftn-1, ads-1, and gpx-6 strengthened alterations in ferroptosis related indicators, and RNAi of bli-3 suppressed changes of ferroptosis related indicators in 6-PPDQ exposed nematodes. Meanwhile, RNAi of ftn-1, ads-1, and gpx-6 induced susceptibility, and RNAi of bli-3 caused resistance to 6-PPDQ reproductive toxicity. Moreover, expressions of DNA damage checkpoint genes (clk-2, mrt-2, and hus-1) could be increased by RNAi of ftn-1, ads-1, and gpx-6 in 6-PPDQ exposed nematodes. Therefore, our results demonstrated activation of ferroptosis in nematodes exposed to 6-PPDQ at environmentally relevant concentrations, and this ferroptosis activation was related to reproductive toxicity of 6-PPDQ.

摘要

N-(1,3-二甲基丁基)-N'-苯基对苯二胺醌(6-PPDQ)暴露会导致秀丽隐杆线虫产生毒性,包括生殖毒性。然而,6-PPDQ 诱导生殖毒性的潜在机制在很大程度上仍不清楚。我们研究了铁死亡激活与 6-PPDQ 生殖毒性之间可能的关联。在 1-100μg/L 的 6-PPDQ 暴露线虫中,铁含量增加,伴随着脂质过氧化增强,丙二醛(MDA)含量增加,L-谷胱甘肽(GSH)含量减少。暴露于 1-100μg/L 的 6-PPDQ 会降低编码铁蛋白的 ftn-1、编码 AGPS 的 ads-1 和编码 GPX4 的 gpx-6 的表达,并增加编码双氧化酶的 bli-3 的表达。在 6-PPDQ 暴露后,ftn-1 的 RNAi 降低了 ads-1 和 gpx-6 的表达,并增加了 bli-3 的表达。ftn-1、ads-1 和 gpx-6 的 RNAi 增强了铁死亡相关指标的变化,而 bli-3 的 RNAi 抑制了 6-PPDQ 暴露线虫中铁死亡相关指标的变化。同时,ftn-1、ads-1 和 gpx-6 的 RNAi 诱导了对 6-PPDQ 生殖毒性的敏感性,而 bli-3 的 RNAi 导致了对 6-PPDQ 生殖毒性的抗性。此外,ftn-1、ads-1 和 gpx-6 的 RNAi 可在 6-PPDQ 暴露线虫中增加 DNA 损伤检查点基因(clk-2、mrt-2 和 hus-1)的表达。因此,我们的结果表明,在环境相关浓度的 6-PPDQ 暴露下,线虫中铁死亡的激活与 6-PPDQ 的生殖毒性有关。

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