Department of Biomedical Sciences and Pathobiology, VA-MD College of Veterinary Medicine, Virginia Tech, Blacksburg, VA, United States.
Graduate Program in Translational Biology, Medicine and Health, Virginia Tech, Blacksburg, VA, United States.
Front Immunol. 2019 Nov 28;10:2714. doi: 10.3389/fimmu.2019.02714. eCollection 2019.
Coal is one of the most abundant and economic sources for global energy production. However, the burning of coal is widely recognized as a significant contributor to atmospheric particulate matter linked to deleterious respiratory impacts. Recently, we have discovered that burning coal generates large quantities of otherwise rare Magnéli phase titanium suboxides from TiO minerals naturally present in coal. These nanoscale Magnéli phases are biologically active without photostimulation and toxic to airway epithelial cells and to zebrafish . Here, we sought to determine the clinical and physiological impact of pulmonary exposure to Magnéli phases using mice as mammalian model organisms. Mice were exposed to the most frequently found Magnéli phases, TiO, at 100 parts per million (ppm) via intratracheal administration. Local and systemic titanium concentrations, lung pathology, and changes in airway mechanics were assessed. Additional mechanistic studies were conducted with primary bone marrow derived macrophages. Our results indicate that macrophages are the cell type most impacted by exposure to these nanoscale particles. Following phagocytosis, macrophages fail to properly eliminate Magnéli phases, resulting in increased oxidative stress, mitochondrial dysfunction, and ultimately apoptosis. In the lungs, these nanoparticles become concentrated in macrophages, resulting in a feedback loop of reactive oxygen species production, cell death, and the initiation of gene expression profiles consistent with lung injury within 6 weeks of exposure. Chronic exposure and accumulation of Magnéli phases ultimately results in significantly reduced lung function impacting airway resistance, compliance, and elastance. Together, these studies demonstrate that Magnéli phases are toxic in the mammalian airway and are likely a significant nanoscale environmental pollutant, especially in geographic regions where coal combustion is a major contributor to atmospheric particulate matter.
煤炭是全球能源生产中最丰富和最经济的来源之一。然而,燃烧煤炭被广泛认为是大气颗粒物的主要来源之一,而这些颗粒物与有害的呼吸道影响有关。最近,我们发现,燃烧煤炭会从煤中天然存在的 TiO 矿物产生大量原本罕见的 Magnéli 相钛亚氧化物。这些纳米级的 Magnéli 相在没有光刺激的情况下具有生物活性,对气道上皮细胞和斑马鱼有毒。在这里,我们试图用老鼠作为哺乳动物模型来确定肺部暴露于 Magnéli 相的临床和生理影响。老鼠通过气管内给药暴露于最常见的 Magnéli 相 TiO2 中,浓度为 100 ppm。评估了局部和全身钛浓度、肺病理学和气道力学的变化。还对原代骨髓来源的巨噬细胞进行了额外的机制研究。我们的结果表明,巨噬细胞是受这些纳米颗粒影响最大的细胞类型。吞噬后,巨噬细胞无法正确清除 Magnéli 相,导致氧化应激增加、线粒体功能障碍,最终导致细胞凋亡。在肺部,这些纳米颗粒在巨噬细胞中浓缩,导致活性氧产生、细胞死亡的反馈循环,以及在暴露后 6 周内与肺损伤一致的基因表达谱的启动。慢性暴露和 Magnéli 相的积累最终导致肺功能显著降低,影响气道阻力、顺应性和弹性。总之,这些研究表明,Magnéli 相在哺乳动物气道中是有毒的,并且很可能是一种重要的纳米级环境污染物,尤其是在煤炭燃烧是大气颗粒物主要来源的地区。