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交通污染暴露对DNA甲基化的影响
引用本文:汪婷,丁锐,黄丹妮,祝子逸,章军,叶怀庄,徐迎春,金永堂.交通污染暴露对DNA甲基化的影响[J].环境科学,2017,38(8):3529-3535.
作者姓名:汪婷  丁锐  黄丹妮  祝子逸  章军  叶怀庄  徐迎春  金永堂
作者单位:浙江大学公共卫生学院环境表观遗传实验室, 杭州 310058,浙江大学公共卫生学院环境表观遗传实验室, 杭州 310058,浙江大学公共卫生学院环境表观遗传实验室, 杭州 310058,浙江大学医学院附属邵逸夫医院, 杭州 310058,浙江大学公共卫生学院毒理学研究室, 杭州 310058,浙江大学公共卫生实验教学中心, 杭州 310058,浙江大学药学院生化药学研究室, 杭州 310058,浙江大学公共卫生学院环境表观遗传实验室, 杭州 310058
基金项目:国家自然科学基金项目(81372953,81673124)
摘    要:探讨交通污染现场暴露对DNA甲基化的影响.30只8周龄Wistar大鼠按随机数字表法随机分5组,每组6只.其中3组分别在隧道(高暴露组)、路口(中暴露组)、校园(对照组)暴露7 d,另外2组分别在隧道暴露14 d/28 d.在暴露过程中检测3个暴露地点PM_(10)、NO_2的浓度.暴露实验分别在春季、秋季各进行一次.暴露结束后,焦磷酸测序法检测肺组织和血液中DNA(p53、MGMT、MAGE-A4)甲基化水平,并分析比较不同暴露组间DNA甲基化水平的差异.结果表明,PM_(10)、NO_2浓度均为隧道(高暴露组)路口(中暴露组)校园(对照组),差异具有统计学意义.秋季暴露7 d后,与对照组相比,肺组织中p53(P_(路口)=0.016;P_(隧道)=0.019)、MGMT(P_(路口)=0.002;P_(隧道)=0.003)启动子甲基化水平显著降低,随着暴露时间的增加,甲基化水平进一步降低;MAGE-A4启动子区处于高度甲基化状态,在肺组织和血液中,均未发现MAGE-A4启动子甲基化水平在三暴露组间存在显著的统计学差异.7d暴露对肺组织中DNA甲基化水平的影响更大,但随着暴露时间的增加,肺组织和血液中DNA甲基化水平改变模式趋于一致.Spearman相关分析结果显示,在肺组织中,PM_(10)和p53甲基化水平呈负相关关系(r=-0.347;P=0.038);NO_2和p53、MGMT、MAGE-A4甲基化水平均存在负相关(r值分别为-0.482、-0.444、-0.346,P值均0.05).在血液中,MAGE-A4甲基化水平与PM_(10)、NO_2均呈正相关(r值分别为0.395、0.431,P值均0.05).交通污染暴露会引起p53、MGMT启动子低甲基化.

关 键 词:交通污染  DNA甲基化  p  53  MGMT  暴露
收稿时间:2017/1/11 0:00:00
修稿时间:2017/3/7 0:00:00

Effects of Traffic-related Air Pollution Exposure on DNA Methylation
WANG Ting,DING Rui,HUANG Dan-ni,ZHU Zi-yi,ZHANG Jun,YE Huai-zhuang,XU Ying-chun and JIN Yong-tang.Effects of Traffic-related Air Pollution Exposure on DNA Methylation[J].Chinese Journal of Environmental Science,2017,38(8):3529-3535.
Authors:WANG Ting  DING Rui  HUANG Dan-ni  ZHU Zi-yi  ZHANG Jun  YE Huai-zhuang  XU Ying-chun and JIN Yong-tang
Institution:Environmental Epigenetics Laboratory, Department of Environmental Medicine, School of Medicine, Zhejiang University, Hangzhou 310058, China,Environmental Epigenetics Laboratory, Department of Environmental Medicine, School of Medicine, Zhejiang University, Hangzhou 310058, China,Environmental Epigenetics Laboratory, Department of Environmental Medicine, School of Medicine, Zhejiang University, Hangzhou 310058, China,Department of Cardiothoracic Surgery, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University, Hangzhou 310058, China,Department of Toxicology, School of Medicine, Zhejiang University, Hangzhou 310058, China,Public Health Experimental Teaching Center, Zhejiang University, Hangzhou 310058, China,School of Pharmacology, Zhejiang University, Hangzhou 310058, China and Environmental Epigenetics Laboratory, Department of Environmental Medicine, School of Medicine, Zhejiang University, Hangzhou 310058, China
Abstract:The goal of the present study was to explore the effects of traffic-related air pollution exposure on DNA methylation. Into five groups of 6, 30 healthy Wistar rats were randomly divided. Three groups of rats were then exposed to traffic-related air pollution at high (tunnel), moderate (crossroad), and low (control) pollution levels for 7 d, whereas the two other groups were exposed in the tunnel for 14 d/28 d. The levels of PM10 and NO2 were measured during the exposure. The study was performed in spring and autumn, and lung tissue and blood were collected after the exposure. Promoter methylation levels of p 53 , MGMT, and MAGE-A 4 were quantified via pyrosequencing. The levels of PM10 and NO2 in the crossroad and tunnel groups were significantly higher than those in the control group. After 7 d exposure in autumn, promoter methylation levels of p 53 and MGMT in lung tissue significantly decreased, and the methylation status continued to decrease with increasing exposure time; MAGE-A 4 was highly methylated and showed no difference among the three groups. DNA methylation in lung tissue was more likely to be changed compared with that in blood during 7 d exposure. As the exposure time increased, DNA methylation changes between blood and lung tissue started to coincide. In lung tissue, PM10 exposure was significantly associated with decreased p 53 promoter methylation (r=-0.347, P=0.038) and NO2 exposure was significantly associated with decreased promoter methylation of p 53, MGMT, and MAGE-A 4 (r=-0.482, -0.444, and -0.346, respectively; P< 0.05). In blood, PM10 and NO2 were significantly and positively associated with MAGE-A 4 promoter methylation (r=0.395 and 0.431, respectively; P< 0.05). Traffic-related air pollution exposure may induce promoter hypomethylation of p 53 and MGMT.
Keywords:traffic-related air pollution  DNA methylation  p 53  MGMT  exposure
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