Oxidative stress and inflammation generated DNA damage by exposure to air pollution particles

被引:271
作者
Moller, Peter [1 ]
Danielsen, Pernille Heigh [1 ]
Karottki, Donna Gabriela [1 ]
Jantzen, Kim [1 ]
Roursgaard, Martin [1 ]
Klingberg, Henrik [1 ]
Jensen, Ditte Marie [1 ]
Christophersen, Daniel Vest [1 ]
Hemmingsen, Jette Gjerke [1 ]
Cao, Yi [1 ]
Loft, Steffen [1 ]
机构
[1] Univ Copenhagen, Dept Publ Hlth, Environm Hlth Sect, DK-1014 Copenhagen K, Denmark
关键词
Biomonitoring; Comet assay; Inflammation; ROS production; Animal models; Cell culture; AMBIENT PARTICULATE MATTER; POLYCYCLIC AROMATIC-HYDROCARBONS; EXHALED NITRIC-OXIDE; URBAN AIRBORNE PARTICULATE; DIESEL EXHAUST PARTICLES; LUNG EPITHELIAL-CELLS; C-REACTIVE PROTEIN; SPONTANEOUSLY HYPERTENSIVE-RATS; NASAL RESPIRATORY EPITHELIUM; FREE-RADICAL ACTIVITY;
D O I
10.1016/j.mrrev.2014.09.001
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Generation of oxidatively damaged DNA by particulate matter (PM) is hypothesized to occur via production of reactive oxygen species (ROS) and inflammation. We investigated this hypothesis by comparing ROS production, inflammation and oxidatively damaged DNA in different experimental systems investigating air pollution particles. There is substantial evidence indicating that exposure to air pollution particles was associated with elevated levels of oxidatively damaged nucleobases in circulating blood cells and urine from humans, which is supported by observations of elevated levels of genotoxicity in cultured cells exposed to similar PM. Inflammation is most pronounced in cultured cells and animal models, whereas an elevated level of oxidatively damaged DNA is more pronounced than inflammation in humans. There is non-congruent data showing corresponding variability in effect related to PM sampled at different locations (spatial variability), times (temporal variability) or particle size fraction across different experimental systems of acellular conditions, cultured cells, animals and humans. Nevertheless, there is substantial variation in the genotoxic, inflammation and oxidative stress potential of PM sampled at different locations or times. Small air pollution particles did not appear more hazardous than larger particles, which is consistent with the notion that constituents such as metals and organic compounds also are important determinants for PM-generated oxidative stress and inflammation. In addition, the results indicate that PM-mediated ROS production is involved in the generation of inflammation and activated inflammatory cells can increase their ROS production. The observations indicate that air pollution particles generate oxidatively damaged DNA by promoting a milieu of oxidative stress and inflammation. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:133 / 166
页数:34
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