Pro-inflammatory effects of inhaled Great Salt Lake dust particles.

IF 7.2 1区 医学 Q1 TOXICOLOGY Particle and Fibre Toxicology Pub Date : 2025-01-16 DOI:10.1186/s12989-025-00618-9
Jacob M Cowley, Cassandra E Deering-Rice, John G Lamb, Erin G Romero, Marysol Almestica-Roberts, Samantha N Serna, Lili Sun, Kerry E Kelly, Ross T Whitaker, Jenna Cheminant, Alessandro Venosa, Christopher A Reilly
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Abstract

Background: Climate change and human activities have caused the drying of marine environments around the world. An example is the Great Salt Lake in Utah, USA which is at a near record low water level. Adverse health effects have been associated with exposure to windblown dust originating from dried lakebed sediments, but mechanistic studies evaluating the health effects of these dusts are limited.

Results: Monitoring data and images highlight the impact of local crustal and Great Salt Lake sediment dusts on the Salt Lake Valley/Wasatch front airshed. Great Salt Lake sediment and derived PM< 3.1 (quasi-PM2.5 or qPM2.5) contained metals/salts, natural and anthropogenic chemicals, and bacteria. Exposure of mice via inhalation and oropharyngeal aspiration caused neutrophilia, increased expression of mRNA for Il6, Cxcl1, Cxcl2, and Muc5ac in the lungs, and increased IL6 and CXCL1 in bronchoalveolar lavage. Inhaled GSLD qPM2.5 caused a greater neutrophilic response than coal fly ash qPM2.5 and was more cytotoxic to human airway epithelial cells (HBEC3-KT) in vitro. Pro-inflammatory biomarker mRNA induction was replicated in vitro using HBEC3-KT and differentiated monocyte-derived (macrophage-like) THP-1 cells. In HBEC3-KT cells, IL6 and IL8 (the human analogue of Cxcl1 and Cxcl2) mRNA induction was attenuated by ethylene glycol-bis(β-aminoethyl ether)-N, N,N',N'-tetraacetic acid (EGTA) and ruthenium red (RR) co-treatment, and by TRPV1 and TRPV3 antagonists, but less by the Toll-like Receptor-4 (TLR4) inhibitor TAK-242 and deferoxamine. Accordingly, GSLD qPM2.5 activated human TRPV1 as well as other human TRP channels. Dust from the Salton Sea playa (SSD qPM2.5) also stimulated IL6 and IL8 mRNA expression and activated TRPV1 in vitro, but inhibition by TRPV1 and V3 antagonists was dose dependent. Alternatively, responses of THP-1 cells to the Great Salt Lake and Salton Sea dusts were partially mediated by TLR4 as opposed to TRPV1. Finally, "humanized" Trpv1N606D mice exhibited greater neutrophilia than C57Bl/6 mice following GSLD qPM2.5 inhalation.

Conclusions: Dust from the GSL playa and similar dried lakebeds may affect human respiratory health via activation of TRPV1, TRPV3, TLR4, and oxidative stress.

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吸入大盐湖粉尘颗粒的促炎作用。
背景:气候变化和人类活动导致了全球海洋环境的干燥。美国犹他州的大盐湖就是一个例子,它的水位接近历史最低水平。不良的健康影响与接触来自干湖床沉积物的风吹粉尘有关,但评估这些粉尘对健康影响的机制研究有限。结果:监测数据和图像突出了当地地壳和大盐湖沉积物粉尘对盐湖山谷/瓦萨奇前缘大气的影响。大盐湖沉积物和衍生PM(准pm2.5或qPM2.5)含有金属/盐、自然和人为化学物质以及细菌。吸入和口咽吸入暴露小鼠引起嗜中性粒细胞增多,肺中Il6、Cxcl1、Cxcl2和Muc5ac mRNA表达增加,支气管肺泡灌洗液中Il6和Cxcl1表达增加。吸入GSLD qPM2.5比煤粉煤灰qPM2.5引起更大的中性粒细胞反应,并且对体外人气道上皮细胞(HBEC3-KT)具有更大的细胞毒性。使用HBEC3-KT和分化的单核细胞来源(巨噬细胞样)THP-1细胞体外复制促炎生物标志物mRNA诱导。在HBEC3-KT细胞中,乙二醇-双(β-氨基乙醚)-N, N,N‘,N’-四乙酸(EGTA)和钌红(RR)以及TRPV1和TRPV3拮抗剂可减弱il - 6和il - 8 (Cxcl1和Cxcl2的人类似物)mRNA的诱导,但toll样受体-4 (TLR4)抑制剂TAK-242和去铁胺的诱导作用较弱。因此,GSLD qPM2.5激活了人类TRPV1以及其他人类TRP通道。来自Salton Sea playa的粉尘(SSD qPM2.5)也刺激IL6和IL8 mRNA的表达并激活TRPV1,但TRPV1和V3拮抗剂的抑制作用是剂量依赖性的。另外,THP-1细胞对大盐湖和索尔顿海粉尘的反应部分是由TLR4介导的,而不是TRPV1。最后,吸入GSLD qPM2.5后,“人源化”的Trpv1N606D小鼠比C57Bl/6小鼠表现出更大的中性粒细胞。结论:来自GSL干湖和类似干湖床的粉尘可能通过激活TRPV1、TRPV3、TLR4和氧化应激影响人类呼吸系统健康。
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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.
期刊最新文献
Pro-inflammatory effects of inhaled Great Salt Lake dust particles. Deciphering key nano-bio interface descriptors to predict nanoparticle-induced lung fibrosis. Integrated hepatic transcriptomics and metabolomics identify Pck1 as a key factor in the broad dysregulation induced by vehicle pollutants. Hazard assessment of nanomaterials: how to meet the requirements for (next generation) risk assessment. Impact on murine neurodevelopment of early-life exposure to airborne ultrafine carbon nanoparticles.
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