Chen Haoxuan, Harui Airi, Feng Yu, Li Liqiao, Patel Saagar, Schmidt Jacob, Roth Michael D, Zhu Yifang
Department of Environmental Health Sciences, Jonathan and Karin Fielding School of Public Health, University of California, Los Angeles, California 90095, United States.
Division of Pulmonary and Critical Care, Department of Medicine, David Geffen School of Medicine, University of California, Los Angeles, California 90095, United States.
Environ Sci Technol. 2024 Dec 31;58(52):22919-22929. doi: 10.1021/acs.est.4c08315. Epub 2024 Dec 16.
Traditional in vitro and in vivo models for inhalation toxicology studies often fail to replicate the anatomical and physiological conditions of the human lung. This limitation hinders our understanding of intrapulmonary exposures and their related health effects. To address this gap, we developed a ventilated artificial lung system that replicates human inhalation exposures in four key aspects: (1) facilitating continuous breathing with adjustable respiratory parameters; (2) distributing inhaled aerosols through transitional airflow fields in 3D-printed airway structures, which enables size-dependent particle deposition; (3) duplicating the warm and humid lung environment to promote inhaled aerosol dynamics, such as hygroscopic growth; and (4) supporting the cultivation of human airway epithelium for aerosol exposure and toxicological analyses. As a proof-of-concept application, we exposed human bronchial epithelial cells to electronic cigarette aerosols in the system. Our results show that electronic cigarette particles undergo significant hygroscopic growth within the artificial lung, leading to a 19% greater deposition dose compared to data collected at room temperature and relative humidity. Additionally, short-term exposure altered epithelial production of the chemokine Fractalkine in a nicotine-dependent manner, but no acute toxic effects were observed. This artificial lung system provides a more physiologically relevant in vitro model for studying inhalation exposures.
传统的用于吸入毒理学研究的体外和体内模型往往无法复制人类肺部的解剖和生理条件。这一局限性阻碍了我们对肺内暴露及其相关健康影响的理解。为了弥补这一差距,我们开发了一种通气人工肺系统,该系统在四个关键方面复制了人类吸入暴露情况:(1)通过可调节的呼吸参数促进持续呼吸;(2)在3D打印的气道结构中通过过渡气流场分布吸入的气溶胶,这使得颗粒沉积具有尺寸依赖性;(3)复制温暖潮湿的肺部环境以促进吸入气溶胶的动态变化,如吸湿增长;(4)支持培养人气道上皮细胞以进行气溶胶暴露和毒理学分析。作为概念验证应用,我们在该系统中将人支气管上皮细胞暴露于电子烟气溶胶中。我们的结果表明,电子烟颗粒在人工肺内经历显著的吸湿增长,与在室温和相对湿度下收集的数据相比,沉积剂量增加了19%。此外,短期暴露以尼古丁依赖的方式改变了趋化因子Fractalkine的上皮产生,但未观察到急性毒性作用。这种人工肺系统为研究吸入暴露提供了一个更具生理相关性的体外模型。