Department of Health Management, Fujian Health College, Fuzhou, China.
Department of Preventive Medicine, Fujian Provincial Key Laboratory of Environment Factors and Cancer, School of Public Health, Fujian Medical University, Fuzhou, China.
Environ Toxicol. 2020 Dec;35(12):1364-1373. doi: 10.1002/tox.23001. Epub 2020 Jul 21.
There is emerging evidence suggesting that oxidative stress and DNA methylation can alter miRNA expression. However, little is known on the mechanism of miR-17-5p expression changes in paraquat (PQ)-induced nerve cell damage. In the present study, neuro-2a cells were pretreated with antioxidant N-acetylcysteine (NAC) or DNA methylation inhibitor decitabine (DAC), then exposed to different concentrations of PQ, while the expression levels of miR-17-5p were detected by qRT-PCR. Here, it is showed that PQ downregulated the expression of miR-17-5p dose-dependently in neuro-2a cells. The DNA methylation level was upregulated after PQ exposure, while downregulated with the pretreatment of NAC in the above content, detected by 5-mC immunofluorescence technique. The interaction effect of NAC and PQ in alternating DNA methylation level was further confirmed by flow cytometry. NAC and DAC individually had an interaction effect in PQ-induced nerve cell damage. After using NAC, PQ-induced ROS elevation and DNA methylation are reduced, thereby preventing the proapoptotic effect of miR-17-5p. Above all, PQ can induce DNA methylation variations through ROS production, leading to the downregulation of miR-17-5p expression in PQ-induced nerve cell damage.
有新的证据表明,氧化应激和 DNA 甲基化可以改变 miRNA 的表达。然而,关于百草枯(PQ)诱导的神经细胞损伤中 miR-17-5p 表达变化的机制知之甚少。在本研究中,用抗氧化剂 N-乙酰半胱氨酸(NAC)或 DNA 甲基化抑制剂地西他滨(DAC)预处理神经母细胞瘤细胞(Neuro-2a),然后用不同浓度的 PQ 处理,同时通过 qRT-PCR 检测 miR-17-5p 的表达水平。结果表明,PQ 呈剂量依赖性地下调神经母细胞瘤细胞中 miR-17-5p 的表达。PQ 暴露后 DNA 甲基化水平上调,而用 NAC 预处理则下调,通过 5-mC 免疫荧光技术检测。流式细胞术进一步证实了 NAC 和 PQ 在交替 DNA 甲基化水平方面的相互作用效应。NAC 和 DAC 单独对 PQ 诱导的神经细胞损伤具有相互作用效应。使用 NAC 后,PQ 诱导的 ROS 升高和 DNA 甲基化减少,从而阻止了 miR-17-5p 的促凋亡作用。综上所述,PQ 可以通过产生 ROS 诱导 DNA 甲基化变化,导致 PQ 诱导的神经细胞损伤中 miR-17-5p 表达下调。