Department of Public Health, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Science, Okayama, Japan.
Third Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health Japan, Kitakyushu, Japan.
Environ Toxicol. 2019 Jul;34(7):836-843. doi: 10.1002/tox.22751. Epub 2019 Apr 5.
The synergic allergic inflammatory effects of particulate matter (PM) 2.5 and human albumin were investigated in NC/Nga mice, which are hypersensitive to mite allergens. PM2.5 or PM2.5 plus human albumin with aluminum oxide was injected twice intraperitoneally for sensitization. After 7 days, PM2.5 or PM2.5 plus human albumin was administered five times intranasally to mice for further sensitization. Subsequently, PM2.5 was administered as a challenge on the 11th day. On the 12th day, mice were examined for airway hyperresponsiveness (AHR), bronchoalveolar lavage fluid (BALF) cell count, mRNA expression of Th , Th cytokines, chemokines, and mucus proteins (MUC5AC and MUC5B) in the lung tissue and histopathology. Although PM2.5 or human albumin alone did not induce allergic airway inflammation, simultaneous inoculation of PM2.5 and human albumin-induced airway inflammation showing increase in AHR, total BALF cell numbers, mRNA levels of IL-13, eotaxin 1, eotaxin 2, and MUC5AC, and anti-IG against human serum albumin. Inflammation was observed around the bronchus in PM2.5 plus human albumin-induced lungs. These results demonstrate that PM2.5 can induce allergic airway inflammation through the synergistic action with human albumin in NC/Nga mice.
研究了细颗粒物(PM2.5)和人白蛋白对螨变应原过敏的 NC/Nga 小鼠的协同过敏炎症作用。PM2.5 或 PM2.5 与人白蛋白加氧化铝两次腹腔内注射进行致敏。7 天后,PM2.5 或 PM2.5 与人白蛋白加氧化铝五次鼻腔内给药以进一步致敏。随后,在第 11 天给予 PM2.5 作为挑战。第 12 天,检查小鼠气道高反应性(AHR)、支气管肺泡灌洗液(BALF)细胞计数、肺组织中 Th1、Th2 细胞因子、趋化因子和粘蛋白(MUC5AC 和 MUC5B)的 mRNA 表达以及组织病理学变化。尽管 PM2.5 或人白蛋白单独使用不会引起过敏气道炎症,但同时接种 PM2.5 和人白蛋白会引起气道炎症,表现为 AHR、总 BALF 细胞数、IL-13、嗜酸性粒细胞趋化因子 1、嗜酸性粒细胞趋化因子 2 和 MUC5AC 的 mRNA 水平以及针对人血清白蛋白的抗体增加。在 PM2.5 加人白蛋白诱导的肺部中,可以观察到支气管周围的炎症。这些结果表明,PM2.5 可以通过与人白蛋白在 NC/Nga 小鼠中的协同作用诱导过敏气道炎症。