Copper-enriched automotive brake wear particles perturb human alveolar cellular homeostasis.

IF 8.2 1区 医学 Q1 TOXICOLOGY
James G H Parkin, Lareb S N Dean, Joseph A Bell, Natasha H C Easton, Liam J Edgeway, Matthew J Cooper, Robert Ridley, Franco Conforti, Siyuan Wang, Liudi Yao, Juanjuan Li, Helen Vethakan Raj, Julian Downward, Miriam Gerlofs-Nijland, Flemming R Cassee, Yihua Wang, Richard B Cook, Mark G Jones, Donna E Davies, Matthew Loxham
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引用次数: 0

Abstract

Background: Airborne fine particulate matter with diameter < 2.5 μm (PM2.5), can reach the alveolar regions of the lungs, and is associated with over 4 million premature deaths per year worldwide. However, the source-specific consequences of PM2.5 exposure remain poorly understood. A major, but unregulated source is car brake wear, which exhaust emission reduction measures have not diminished.

Methods: We used an interdisciplinary approach to investigate the consequences of brake-wear PM2.5 exposure upon lung alveolar cellular homeostasis using diesel exhaust PM as a comparator. This involved RNA-Seq to analyse global transcriptomic changes, metabolic analyses to investigate glycolytic reprogramming, mass spectrometry to determine PM composition, and reporter assays to provide mechanistic insight into differential effects.

Results: We identified brake-wear PM from copper-enriched non-asbestos organic, and ceramic brake pads as inducing the greatest oxidative stress, inflammation, and pseudohypoxic HIF activation (a pathway implicated in diseases associated with air pollution exposure, including cancer, and pulmonary fibrosis), as well as perturbation of metabolism, and metal homeostasis compared with brake wear PM from low- or semi-metallic pads, and also, importantly, diesel exhaust PM. Compositional and metal chelator analyses identified that differential effects were driven by copper.

Conclusions: We demonstrate here that brake-wear PM may perturb cellular homeostasis more than diesel exhaust PM. Our findings demonstrate the potential differences in effects, not only for non-exhaust vs exhaust PM, but also amongst different sources of non-exhaust PM. This has implications for our understanding of the potential health effects of road vehicle-associated PM. More broadly, our findings illustrate the importance of PM composition on potential health effects, highlighting the need for targeted legislation to protect public health.

Abstract Image

Abstract Image

Abstract Image

富铜汽车刹车磨损颗粒扰乱人肺泡细胞稳态。
背景:空气中的细颗粒物直径方法:我们采用跨学科的方法,以柴油排放的PM为比较物,研究了PM2.5暴露对肺泡细胞稳态的影响。这包括分析全局转录组变化的RNA-Seq,研究糖酵解重编程的代谢分析,确定PM组成的质谱分析,以及提供差异效应机制的报告分析。结果:我们发现,与低金属或半金属刹车片产生的刹车片磨损PM相比,富铜非石棉有机刹车片和陶瓷刹车片产生的刹车片磨损PM诱导最大的氧化应激、炎症和假性缺氧HIF激活(一种与空气污染暴露相关的疾病,包括癌症和肺纤维化有关的途径),以及代谢扰动和金属稳态,更重要的是,与柴油排放的PM相比。成分分析和金属螯合剂分析表明,不同的影响是由铜驱动的。结论:我们在这里证明了制动磨损PM可能比柴油排气PM更能扰乱细胞稳态。我们的研究结果证明了影响的潜在差异,不仅是非废气PM与废气PM,而且是非废气PM的不同来源。这对我们理解道路车辆相关的PM对健康的潜在影响具有启示意义。更广泛地说,我们的研究结果说明了PM成分对潜在健康影响的重要性,强调了有针对性立法保护公众健康的必要性。
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来源期刊
CiteScore
15.90
自引率
4.00%
发文量
69
审稿时长
6 months
期刊介绍: Particle and Fibre Toxicology is an online journal that is open access and peer-reviewed. It covers a range of disciplines such as material science, biomaterials, and nanomedicine, focusing on the toxicological effects of particles and fibres. The journal serves as a platform for scientific debate and communication among toxicologists and scientists from different fields who work with particle and fibre materials. The main objective of the journal is to deepen our understanding of the physico-chemical properties of particles, their potential for human exposure, and the resulting biological effects. It also addresses regulatory issues related to particle exposure in workplaces and the general environment. Moreover, the journal recognizes that there are various situations where particles can pose a toxicological threat, such as the use of old materials in new applications or the introduction of new materials altogether. By encompassing all these disciplines, Particle and Fibre Toxicology provides a comprehensive source for research in this field.
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