Proinflammatory effects and oxidative stress within human bronchial epithelial cells exposed to atmospheric particulate matter (PM2.5 and PM>2.5) collected from Cotonou, Benin

被引:134
作者
Cachon, Boris Fresnel [1 ,2 ,3 ]
Firmin, Stephane [2 ,4 ]
Verdin, Anthony [2 ]
Ayi-Fanou, Lucie [3 ]
Billet, Sylvain [1 ,2 ]
Cazier, Fabrice [1 ,5 ]
Martin, Perrine J. [1 ,2 ]
Aissi, Faustin [1 ]
Courcot, Dominique [1 ,2 ]
Sanni, Ambaliou [3 ]
Shirali, Pirouz [1 ,2 ]
机构
[1] Univ Lille Nord France, Lille, France
[2] Univ Littoral Cote dOpale, UCEIV, EA 4492, Maison Rech Environm Ind 2, F-59140 Dunkerque, France
[3] Univ Abomey Calavi, Fac Sci & Tech, Lab Biochim & Biol Mol, Cotonou, Benin
[4] Inst Polytech LaSalle Beauvais, UPSP EGEAL, F-60026 Beauvais, France
[5] Univ Littoral Cote dOpale, Ctr Commun Mesures Maison Rech & Environm Ind 1, F-59140 Dunkerque, France
关键词
Benin; Cytotoxicity; Inflammatory response; Oxidative stress; Particulate matter; URBAN AIR-POLLUTION; IN-VITRO; PHYSICOCHEMICAL CHARACTERIZATION; CARDIOVASCULAR-DISEASE; CHEMICAL-COMPOSITION; SOURCE APPORTIONMENT; CHEMOKINE RESPONSES; ORGANIC EXTRACTS; LUNG-CANCER; A549; CELLS;
D O I
10.1016/j.envpol.2013.10.026
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
After particulate matter (PM) collection in Cotonou (Benin), a complete physicochemical characterization of PM2.5 and PM>2.5 was led. Then, their adverse health effects were evaluated by using in vitro culture of human lung cells. BEAS-2B (bronchial epithelial cells) were intoxicated during short-term exposure at increasing PM concentrations (1.5-96 mu g/cm(2)) to determine global cytotoxicity. Hence, cells were exposed to 3 and 12 mu g/cm(2) to investigate the potential biological imbalance generated by PM toxicity. Our findings showed the ability of both PM to induce oxidative stress and to cause inflammatory cytokines/chemokines gene expression and secretion. Furthermore, PM were able to induce gene expression of enzymes involved in the xenobiotic metabolism pathway. Strong correlations between gene expression of metabolizing enzymes, proinflammatory responses and cell cycle alteration were found, as well as between proinflammatory responses and cell viability. Stress oxidant parameters were highly correlated with expression and protein secretion of inflammatory mediators. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:340 / 351
页数:12
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