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首页> 外文期刊>Particle Fibre Toxicology >Endothelial responses of the alveolar barrier in vitro in a dose-controlled exposure to diesel exhaust particulate matter
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Endothelial responses of the alveolar barrier in vitro in a dose-controlled exposure to diesel exhaust particulate matter

机译:剂量控制性暴露于柴油机废气颗粒物中时肺泡屏障的内皮反应

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BackgroundDuring the last 250?years, the level of exposure to combustion-derived particles raised dramatically in western countries, leading to increased particle loads in the ambient air. Among the environmental particles, diesel exhaust particulate matter (DEPM) plays a special role because of its omnipresence and reported effects on human health. During recent years, a possible link between air pollution and the progression of atherosclerosis is recognized. A central effect of DEPM is their impact on the endothelium, especially of the alveolar barrier. In the present study, a complex 3D tetraculture model of the alveolar barrier was used in a dose-controlled exposure scenario with realistic doses of DEPM to study the response of endothelial cells. ResultsTetracultures were exposed to different doses of DEPM (SRM2975) at the air-liquid-interface. DEPM exposure did not lead to the mRNA expression of relevant markers for endothelial inflammation such as ICAM-1 or E-selectin . In addition, we observed neither a significant change in the expression levels of the genes relevant for antioxidant defense, such as HMOX1 or SOD1 , nor the release of pro-inflammatory second messengers, such as IL-6 or IL-8 . However, DEPM exposure led to strong nuclear translocation of the transcription factor Nrf2 and significantly altered expression of CYP1A1 mRNA in the endothelial cells of the tetraculture. ConclusionIn the present study, we demonstrated the use of a complex 3D tetraculture system together with a state-of-the-art aerosol exposure equipment to study the effects of in vivo relevant doses of DEPM on endothelial cells in vitro. To the best of our knowledge, this study is the first that focuses on indirect effects of DEPM on endothelial cells of the alveolar barrier in vitro. Exposure to DEPM led to significant activation and nuclear translocation of the transcription factor Nrf2 in endothelial cells. The considerably low doses of DEPM had a low but measurable effect, which is in line with recent data from in vivo studies.
机译:背景技术在过去的250年中,西方国家接触燃烧产生的颗粒的水平急剧上升,导致周围空气中的颗粒负荷增加。在环境颗粒中,柴油机排气颗粒物(DEPM)由于其无处不在并据报道对人体健康具有特殊作用。近年来,人们认识到空气污染与动脉粥样硬化进展之间可能存在联系。 DEPM的主要作用是它们对内皮的影响,尤其是对肺泡屏障的影响。在本研究中,在实际剂量的DEPM剂量控制的暴露情况下,使用了肺泡屏障的复杂3D四培养模型来研究内皮细胞的反应。结果四培养物在气液界面处暴露于不同剂量的DEPM(SRM2975)。暴露于DEPM并未导致内皮炎症相关标志物(ICAM-1或E-选择素)的mRNA表达。此外,我们既没有观察到与抗氧化剂防御相关的基因(如HMOX1或SOD1)的表达水平发生显着变化,也没有观察到促炎性第二信使(如IL-6或IL-8)的释放。然而,DEPM暴露导致转录因子Nrf2的强烈核易位,并显着改变CYP1A1 mRNA在四次培养的内皮细胞中的表达。结论在本研究中,我们证明了使用复杂的3D四培养系统和最先进的气溶胶暴露设备来研究体内相关剂量的DEPM对体外内皮细胞的影响。据我们所知,这项研究是第一个侧重于DEPM对体外肺泡屏障内皮细胞间接作用的研究。暴露于DEPM会导致内皮细胞中转录因子Nrf2的显着活化和核易位。相当低的DEPM剂量具有低但可测量的作用,这与来自体内研究的最新数据一致。

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