Key Laboratory of Modern Toxicology of Shenzhen, Medical Key Laboratory of Guangdong Province, Medical Key Laboratory of Health Toxicology of Shenzhen, Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, China; School of Life Science, Shenzhen University, Shenzhen 518060, China.
Key Laboratory of Modern Toxicology of Shenzhen, Medical Key Laboratory of Guangdong Province, Medical Key Laboratory of Health Toxicology of Shenzhen, Shenzhen Center for Disease Control and Prevention, Shenzhen 518055, China.
Biochem Biophys Res Commun. 2014 Apr 4;446(2):590-5. doi: 10.1016/j.bbrc.2014.03.015. Epub 2014 Mar 13.
Trichloroethylene (TCE), a major occupational and environmental pollutant, has been recently associated with aberrant epigenetic changes in experimental animals and cultured cells. TCE is known to cause severe hepatotoxicity; however, the association between epigenetic alterations and TCE-induced hepatotoxicity are not yet well explored. DNA methylation, catalyzed by enzymes known as DNA methyltransferases (DNMT), is a major epigenetic modification that plays a critical role in regulating many cellular processes. In this study, we analyzed the TCE-induced effect on global DNA methylation and DNMT enzymatic activity in human hepatic L-02 cells. A sensitive and quantitative method combined with liquid chromatography and electrospray ionization tandem mass spectrometry (LC-ESI-MS/MS) was validated and utilized for assessing the altered DNA methylation in TCE-induced L-02 cells. Quantification was accomplished in multiple reaction monitoring (MRM) mode by monitoring a transition pair of m/z 242.1 (molecular ion)/126.3 (fragment ion) for 5-mdC and m/z 268.1/152.3 for dG. The correlation coefficient of calibration curves between 5-mdC and dG was higher than 0.9990. The intra-day and inter-day relative standard derivation values (RSD) were on the range of 0.53-7.09% and 0.40-2.83%, respectively. We found that TCE exposure was able to significantly decrease the DNA methylation and inhibit DNMT activity in L-02 cells. Our results not only reveal the association between TCE exposure and epigenetic alterations, but also provide an alternative mass spectrometry-based method for rapid and accurate assessment of chemical-induced altered DNA methylation in mammal cells.
三氯乙烯(TCE)是一种主要的职业和环境污染物,最近与实验动物和培养细胞中的异常表观遗传变化有关。TCE 已知会引起严重的肝毒性;然而,表观遗传改变与 TCE 诱导的肝毒性之间的关联尚未得到充分探索。DNA 甲基化由称为 DNA 甲基转移酶(DNMT)的酶催化,是一种主要的表观遗传修饰,在调节许多细胞过程中起着关键作用。在这项研究中,我们分析了 TCE 对人肝 L-02 细胞中全局 DNA 甲基化和 DNMT 酶活性的诱导作用。一种灵敏且定量的方法与液相色谱和电喷雾串联质谱(LC-ESI-MS/MS)相结合,已被验证并用于评估 TCE 诱导的 L-02 细胞中改变的 DNA 甲基化。通过监测 m/z 242.1(分子离子)/126.3(片段离子)对 5-mdC 和 m/z 268.1/152.3 对 dG 的跃迁对,在多重反应监测(MRM)模式下完成定量。5-mdC 和 dG 之间校准曲线的相关系数大于 0.9990。日内和日间相对标准偏差(RSD)分别在 0.53-7.09%和 0.40-2.83%的范围内。我们发现 TCE 暴露能够显著降低 L-02 细胞中的 DNA 甲基化并抑制 DNMT 活性。我们的结果不仅揭示了 TCE 暴露与表观遗传改变之间的关联,而且为快速准确评估哺乳动物细胞中化学诱导的改变的 DNA 甲基化提供了一种替代的基于质谱的方法。