Division of Genetic and Molecular Toxicology, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, AR, 72079, USA.
Division of Bioinformatics and Biostatistics, National Center for Toxicological Research, U.S. Food and Drug Administration, Jefferson, 72079, AR, USA.
Arch Toxicol. 2021 May;95(5):1763-1778. doi: 10.1007/s00204-021-03016-0. Epub 2021 Mar 11.
Exposure to cigarette smoke (CS) is strongly associated with impaired mucociliary clearance (MCC), which has been implicated in the pathogenesis of CS-induced respiratory diseases, such as chronic obstructive pulmonary diseases (COPD). In this study, we aimed to identify microRNAs (miRNAs) that are associated with impaired MCC caused by CS in an in vitro human air-liquid-interface (ALI) airway tissue model. ALI cultures were exposed to CS (diluted with 0.5 L/min, 1.0 L/min, and 4.0 L/min of clean air) from smoking five 3R4F University of Kentucky reference cigarettes under the International Organization for Standardization (ISO) machine smoking regimen, every other day for 1 week (a total of 3 days, 40 min/day). Transcriptome analyses of ALI cultures exposed to the high concentration of CS identified 5090 differentially expressed genes and 551 differentially expressed miRNAs after the third exposure. Genes involved in ciliary function and ciliogenesis were significantly perturbed by repeated CS exposures, leading to changes in cilia beating frequency and ciliary protein expression. In particular, a time-dependent decrease in the expression of miR-449a, a conserved miRNA highly enriched in ciliated airway epithelia and implicated in motile ciliogenesis, was observed in CS-exposed cultures. Similar alterations in miR-449a have been reported in smokers with COPD. Network analysis further indicates that downregulation of miR-449a by CS may derepress cell-cycle proteins, which, in turn, interferes with ciliogenesis. Investigating the effects of CS on transcriptome profile in human ALI cultures may provide not only mechanistic insights, but potential early biomarkers for CS exposure and harm.
暴露于香烟烟雾(CS)与纤毛粘液清除功能受损(MCC)密切相关,后者与 CS 引起的呼吸道疾病(如慢性阻塞性肺疾病(COPD))的发病机制有关。在这项研究中,我们旨在确定与 CS 引起的体外人肺泡界面(ALI)气道组织模型中 MCC 受损相关的 microRNAs(miRNAs)。ALI 培养物暴露于 CS(用 0.5 L/min、1.0 L/min 和 4.0 L/min 的清洁空气稀释),每两天接受 5 支 3R4F 肯塔基大学参考香烟的 ISO 机器吸烟方案,每天 40 分钟,共 3 天(共 3 天,每天 40 分钟)。暴露于高浓度 CS 的 ALI 培养物的转录组分析在第三次暴露后确定了 5090 个差异表达基因和 551 个差异表达 miRNA。重复 CS 暴露显着干扰了纤毛功能和纤毛发生相关的基因,导致纤毛摆动频率和纤毛蛋白表达发生变化。特别是,在 CS 暴露的培养物中观察到 miR-449a 的表达呈时间依赖性下降,miR-449a 是一种在气道纤毛上皮中高度富集的保守 miRNA,与运动性纤毛发生有关。在 COPD 吸烟者中也报道了类似的 miR-449a 改变。网络分析进一步表明,CS 下调 miR-449a 可能会解除细胞周期蛋白的抑制,从而干扰纤毛发生。研究 CS 对人 ALI 培养物转录组谱的影响不仅可以提供机制见解,还可以提供 CS 暴露和危害的潜在早期生物标志物。