Effects of Particulate Matter on Genomic DNA Methylation Content and iNOS Promoter Methylation

被引:281
作者
Tarantini, Letizia [2 ,3 ]
Bonzini, Matteo [2 ,3 ]
Apostoli, Pietro [4 ]
Pegoraro, Valeria [2 ,3 ]
Bollati, Valentina [2 ,3 ]
Marinelli, Barbara [2 ,3 ]
Cantone, Laura [2 ,3 ]
Rizzo, Giovanna [2 ,3 ]
Hou, Lifang [5 ]
Schwartz, Joel [6 ]
Bertazzi, Pier Alberto [2 ,3 ]
Baccarelli, Andrea [1 ,2 ,3 ,6 ]
机构
[1] Univ Milan, Lab Environm Epigenet, Dept Environm & Occupat Hlth, I-20122 Milan, Italy
[2] Univ Milan, Lab Environm Epigenet, Dept Prevent Med, I-20122 Milan, Italy
[3] Mangiagalli & Regina Elena Fdn, Maggiore Hosp, IRCCS, Milan, Italy
[4] Univ Brescia, Dept Expt & Appl Med Occupat Med & Ind Hyg, Brescia, Italy
[5] Northwestern Univ, Feinberg Sch Med, Dept Prevent Med, Chicago, IL 60611 USA
[6] Harvard Univ, Sch Publ Hlth, Exposure Epidemiol & Risk Program, Boston, MA 02115 USA
关键词
DNA methylation; epigenetics; etiology; interspersed repetitive sequences; nitric oxide synthase; particulate matter; NITRIC-OXIDE SYNTHASE; CONCENTRATED AMBIENT PARTICLES; HEART-RATE-VARIABILITY; AIR-POLLUTION; GENE-EXPRESSION; FOUNDRY WORKERS; INTRATRACHEAL INSTILLATION; UP-REGULATION; LUNG; MORTALITY;
D O I
10.1289/ehp.11898
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
BACKGROUND: 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. OBJECTIVES: 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 mu m (PM10). METHODS: 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 exposure was between 73.4 and 1,220 mu g/m(3). RESULTS: Global methylation content estimated in Alu and LINE-1 repeated elements did not show changes in postexposure measures compared with baseline. PM10 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 PM10 effects. iNOS promoter DNA methylation was significantly lower in postexposure blood samples compared with baseline (difference = -0.61 %5mC; p = 0.02). CONCLUSIONS: We observed changes in global and gene specific methylation that should be further characterized in future investigations on the effects of PM.
引用
收藏
页码:217 / 222
页数:6
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