Department of Cellular and Molecular Biology, University of Texas Health Science Center at Tyler, Tyler, Texas.
Department of Pulmonary Immunology, University of Texas Health Science Center at Tyler, Tyler, Texas.
Am J Physiol Lung Cell Mol Physiol. 2020 Dec 1;319(6):L893-L907. doi: 10.1152/ajplung.00107.2020. Epub 2020 Sep 30.
Inhalation of organic dust is an occupational hazard leading to the development of respiratory symptoms and respiratory diseases. Bioaerosols from concentrated animal feeding operations are rich in bacteria and could carry bacterial extracellular vesicles (EVs) that could induce lung inflammation. It is not known if organic dust contains bacterial EVs and whether they modulate lung inflammation. Herein, we show that poultry organic dust contains bacterial EVs (dust EVs) that induce lung inflammation. Treatment of airway epithelial cells, THP-1-monocytes and -macrophages with dust EVs rapidly induced IL-8, IL-6, ICAM-1, proIL-1β, and TNF-α levels. In airway epithelial cells, induction of inflammatory mediators was due to increased mRNA levels and NF-κB activation. Induction of inflammatory mediators by dust EVs was not inhibited by polymyxin B. Single and repeated treatments of mice with dust EVs increased lung KC, IL-6, and TNF-α levels without significantly altering IL-17A levels. Increases in cytokines were associated with enhanced neutrophil infiltration into the lung. Repeated treatments of mice with dust EVs increased lung mean linear intercept and increased collagen deposition around airways indicating lung remodeling. Peribronchial cell infiltrates and airway epithelial thickening were also observed in treated mice. Because bacterial EVs are nanometer-sized particles, they can reach and accumulate in the bronchiolar and alveolar regions causing lung injury leading to the development of respiratory diseases. Our studies have provided new evidence for the presence of bacterial EVs in organic dust and for their role as one of the causative agents of organic dust-induced lung inflammation and lung injury.
吸入有机粉尘是一种职业危害,可导致呼吸症状和呼吸道疾病的发生。来自集中式动物饲养作业的生物气溶胶富含细菌,并且可能携带能够诱导肺部炎症的细菌细胞外囊泡(EVs)。目前尚不清楚有机粉尘是否含有细菌 EVs 以及它们是否调节肺部炎症。在此,我们表明家禽有机粉尘含有诱导肺部炎症的细菌 EVs(粉尘 EVs)。用粉尘 EVs 处理气道上皮细胞、THP-1 单核细胞和巨噬细胞可迅速诱导 IL-8、IL-6、ICAM-1、proIL-1β 和 TNF-α水平升高。在气道上皮细胞中,炎症介质的诱导是由于 mRNA 水平的增加和 NF-κB 的激活。粉尘 EVs 诱导炎症介质的产生不受多粘菌素 B 的抑制。用粉尘 EVs 单次和重复处理小鼠可增加肺 KC、IL-6 和 TNF-α 水平,而对 IL-17A 水平没有明显影响。细胞因子的增加与中性粒细胞向肺部的浸润增加有关。用粉尘 EVs 重复处理小鼠可增加肺平均线性截距并增加气道周围的胶原沉积,表明肺重塑。在处理过的小鼠中还观察到细支气管周围细胞浸润和气道上皮增厚。由于细菌 EVs 是纳米级颗粒,它们可以到达并积聚在细支气管和肺泡区域,导致肺部损伤,从而导致呼吸道疾病的发生。我们的研究为有机粉尘中存在细菌 EVs 及其作为有机粉尘诱导的肺部炎症和肺损伤的致病因子之一提供了新的证据。