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In vitro systems toxicology approach to investigate the effects of repeated cigarette smoke exposure on human buccal and gingival organotypic epithelial tissue cultures

机译:体外系统毒理学方法研究反复抽烟对人类颊和牙龈器官型上皮组织培养的影响

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摘要

Smoking has been associated with diseases of the lung, pulmonary airways and oral cavity. Cytologic, genomic and transcriptomic changes in oral mucosa correlate with oral pre-neoplasia, cancer and inflammation (e.g. periodontitis). Alteration of smoking-related gene expression changes in oral epithelial cells is similar to that in bronchial and nasal epithelial cells. Using a systems toxicology approach, we have previously assessed the impact of cigarette smoke (CS) seen as perturbations of biological processes in human nasal and bronchial organotypic epithelial culture models. Here, we report our further assessment using in vitro human oral organotypic epithelium models. We exposed the buccal and gingival organotypic epithelial tissue cultures to CS at the air–liquid interface. CS exposure was associated with increased secretion of inflammatory mediators, induction of cytochrome P450s activity and overall weak toxicity in both tissues. Using microarray technology, gene-set analysis and a novel computational modeling approach leveraging causal biological network models, we identified CS impact on xenobiotic metabolism-related pathways accompanied by a more subtle alteration in inflammatory processes. Gene-set analysis further indicated that the CS-induced pathways in the in vitro buccal tissue models resembled those in the in vivo buccal biopsies of smokers from a published dataset. These findings support the translatability of systems responses from in vitro to in vivo and demonstrate the applicability of oral organotypical tissue models for an impact assessment of CS on various tissues exposed during smoking, as well as for impact assessment of reduced-risk products.
机译:吸烟与肺,肺气道和口腔疾病有关。口腔粘膜的细胞学,基因组和转录组学变化与口腔肿瘤前,癌症和炎症(例如牙周炎)相关。口腔上皮细胞中与吸烟有关的基因表达变化的变化与支气管和鼻上皮细胞中的变化相似。使用系统毒理学方法,我们之前已经评估了香烟烟雾(CS)的影响,该烟雾被视为对人类鼻和支气管器官型上皮培养模型中生物过程的干扰。在这里,我们报告我们使用体外人类口腔器官型上皮模型的进一步评估。我们在气液界面将颊和牙龈器官型上皮组织培养物暴露于CS。 CS暴露与炎性介质的分泌增加,细胞色素P450活性的诱导以及两个组织的总体弱毒性有关。利用微阵列技术,基因组分析和利用因果生物学网络模型的新颖计算模型方法,我们确定了CS对异种代谢相关途径的影响,同时伴随着炎症过程的更细微变化。基因组分析进一步表明,在体外颊组织模型中,CS诱导的途径类似于从已公开的数据集中的吸烟者体内颊活检组织中的途径。这些发现支持了系统反应从体外到体内的可翻译性,并证明了口腔器官典型组织模型可用于CS对吸烟期间暴露于各种组织的影响评估以及降低风险产品的影响评估。

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