Tarantini Letizia, Bonzini Matteo, Apostoli Pietro, Pegoraro Valeria, Bollati Valentina, Marinelli Barbara, Cantone Laura, Rizzo Giovanna, Hou Lifang, Schwartz Joel, Bertazzi Pier Alberto, Baccarelli Andrea
Laboratory of Environmental Epigenetics, Department of Preventive Medicine, University of Milan and IRCCS Maggiore Hospital, Milan, Italy.
Environ Health Perspect. 2009 Feb;117(2):217-22. doi: 10.1289/ehp.11898. Epub 2008 Sep 26.
Altered patterns of gene expression mediate the effects of particulate matter (PM) on human health, but mechanisms through which PM modifies gene expression are largely undetermined.
We aimed at identifying short- and long-term effects of PM exposure on DNA methylation, a major genomic mechanism of gene expression control, in workers in an electric furnace steel plant with well-characterized exposure to PM with aerodynamic diameters < 10 microm (PM(10)).
We measured global genomic DNA methylation content estimated in Alu and long interspersed nuclear element-1 (LINE-1) repeated elements, and promoter DNA methylation of iNOS (inducible nitric oxide synthase), a gene suppressed by DNA methylation and induced by PM exposure in blood leukocytes. Quantitative DNA methylation analysis was performed through bisulfite PCR pyrosequencing on blood DNA obtained from 63 workers on the first day of a work week (baseline, after 2 days off work) and after 3 days of work (postexposure). Individual PM(10) exposure was between 73.4 and 1,220 microg/m(3).
Global methylation content estimated in Alu and LINE-1 repeated elements did not show changes in postexposure measures compared with baseline. PM(10) exposure levels were negatively associated with methylation in both Alu [beta = -0.19 %5-methylcytosine (%5mC); p = 0.04] and LINE-1 [beta = -0.34 %5mC; p = 0.04], likely reflecting long-term PM(10) effects. iNOS promoter DNA methylation was significantly lower in postexposure blood samples compared with baseline (difference = -0.61 %5mC; p = 0.02).
We observed changes in global and gene specific methylation that should be further characterized in future investigations on the effects of PM.
基因表达模式的改变介导了颗粒物(PM)对人类健康的影响,但PM改变基因表达的机制在很大程度上尚未明确。
我们旨在确定在一家空气动力学直径<10微米(PM10)暴露特征明确的电炉钢厂工人中,PM暴露对DNA甲基化(基因表达控制的一种主要基因组机制)的短期和长期影响。
我们测量了在Alu和长散在核元件1(LINE-1)重复元件中估计的全基因组DNA甲基化含量,以及诱导型一氧化氮合酶(iNOS)的启动子DNA甲基化,iNOS是一个在血液白细胞中被DNA甲基化抑制并被PM暴露诱导的基因。通过亚硫酸氢盐PCR焦磷酸测序对从63名工人在工作周的第一天(基线,休息2天后)和工作3天后(暴露后)获得的血液DNA进行定量DNA甲基化分析。个体PM10暴露水平在73.4至1220微克/立方米之间。
与基线相比,Alu和LINE-1重复元件中估计的整体甲基化含量在暴露后测量中未显示变化。PM10暴露水平与Alu[β=-0.19%5-甲基胞嘧啶(%5mC);p=0.04]和LINE-1[β=-0.34%5mC;p=0.04]中的甲基化均呈负相关,可能反映了长期PM10的影响。与基线相比,暴露后血样中iNOS启动子DNA甲基化显著降低(差异=-0.61%5mC;p=0.02)。
我们观察到整体和基因特异性甲基化的变化,这些变化应在未来关于PM影响的研究中进一步表征。