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人离体肺泡巨噬细胞中挥发性有机化合物和/或多环芳烃代谢酶对空气颗粒物(PM2.5)的基因表达诱导作用

Gene expression induction of volatile organic compound and/or polycyclic aromatic hydrocarbon-metabolizing enzymes in isolated human alveolar macrophages in response to airborne particulate matter (PM2.5).

作者信息

Saint-Georges Françoise, Abbas Imane, Billet Sylvain, Verdin Anthony, Gosset Pierre, Mulliez Philippe, Shirali Pirouz, Garçon Guillaume

机构信息

Service de Pneumologie, Hôpital Saint-Philibert, Groupement Hospitalier de l'Institut Catholique-Faculté Libre de Médecine de Lille, rue du Grand But, BP 249, 59462 Lomme Cedex, France.

出版信息

Toxicology. 2008 Feb 28;244(2-3):220-30. doi: 10.1016/j.tox.2007.11.016. Epub 2007 Nov 29.

Abstract

To contribute to improve the knowledge of the underlying mechanisms of action involved in air pollution particulate matter (PM)-induced cytotoxicity, we were interested in the metabolic activation of volatile organic compounds (VOC) and/or polycyclic aromatic hydrocarbons (PAH) coated onto Dunkerque City's PM2.5 in human alveolar macrophages (AM) isolated from bronchoalveolar lavage fluid (BALF). This in vitro cell lung model is closer to the normal in vivo situation than other lung cell lines, notably in the characteristics that AM display in terms of gene expression of phase I and phase II-metabolizing enzymes. The bronchoscopic examinations and BAL procedures were carried out without any complications. After 24, 48 and 72h of incubation, calculated lethal concentrations at 10% and 50% of collected airborne PM were 14.93microg PM/mL and 74.63microg PM/mL, respectively, and indicated the higher sensibility of such target lung cells. Moreover, VOC and/or PAH coated onto PM induced gene expression of cytochrome P450 (cyp) 1a1, cyp2e1, nadph quinone oxydo-reductase-1, and glutathione S-transferase-pi 1 and mu 3, versus controls, suggesting thereby the formation of biologically reactive metabolites. In addition, these results suggested the role of physical carrier of carbonaceous core of PM, which can, therefore, increase both the penetration and the retention of attached-VOC into the cells, thereby enabling them to exert a longer induction. Hence, we concluded that the metabolic activation of the very low doses of VOC and/or PAH coated onto Dunkerque City's PM2.5 is one of the underlying mechanisms of action closely involved in its cytotoxicity in isolated human AM in culture.

摘要

为了有助于增进对空气污染颗粒物(PM)诱导细胞毒性潜在作用机制的了解,我们对从支气管肺泡灌洗液(BALF)中分离出的人肺泡巨噬细胞(AM)中涂覆在敦刻尔克市PM2.5上的挥发性有机化合物(VOC)和/或多环芳烃(PAH)的代谢活化感兴趣。这种体外细胞肺模型比其他肺细胞系更接近正常体内情况,特别是在AM在I相和II相代谢酶基因表达方面所表现出的特征方面。支气管镜检查和BAL操作均无任何并发症。孵育24、48和72小时后,收集的空气中PM的10%和50%致死浓度分别为14.93微克PM/毫升和74.63微克PM/毫升,表明此类靶肺细胞具有较高的敏感性。此外,与对照组相比,涂覆在PM上的VOC和/或PAH诱导了细胞色素P450(cyp)1a1、cyp2e1、还原型辅酶II醌氧化还原酶-1以及谷胱甘肽S-转移酶-pi 1和mu 3的基因表达,从而提示生物活性代谢产物的形成。此外,这些结果表明了PM碳质核心物理载体的作用,因此它可以增加附着的VOC进入细胞的穿透率和保留率,从而使它们能够发挥更长时间的诱导作用。因此,我们得出结论,涂覆在敦刻尔克市PM2.5上的极低剂量VOC和/或PAH的代谢活化是其在培养的分离人AM中细胞毒性密切涉及的潜在作用机制之一。

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