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15天重复空气:液体界面仅空气暴露可导致MucilAir鼻呼吸上皮细胞中的呼吸道上皮损伤,这与化学诱导的细胞毒性相似。

Fifteen day repeat air: liquid Interface air-only exposures can cause respiratory epithelium injury in MucilAir nasal respiratory epithelial cells that parallels chemically induced cytotoxicity.

作者信息

Recio Leslie, Samuel Raymond, Elmore Susan A, Scaglione Jamie

机构信息

ScitoVation LLC, Investigative Toxicology, Durham, NC, USA.

Elmorepathology, LLC, Chapel Hill, NC, USA.

出版信息

Toxicol Mech Methods. 2025 Jan;35(1):81-87. doi: 10.1080/15376516.2024.2382794. Epub 2024 Jul 30.

Abstract

New Approach Methodologies (NAMs) are being widely used to reduce, refine, and replace, animal use in studying toxicology. For respiratory toxicology, this includes and alternatives using air:liquid interface (ALI) exposures to replace traditional inhalation studies. In previous studies using 1,3-dichloropropene (1,3-DCP), a 5-day 4 h repeat exposures of MucilAir nasal cell culture models caused, dose-dependent cytotoxicity, depletion of GSH, changes in differential gene expression and histopathological transitions in cellular morphology from pseudostratified columnar epithelium to squamous epithelium. In this report we attempted to extend these studies using 15-day 1,3-DCP 4 h exposures to using MucilAir nasal cultures as outlined by an US EPA recent task order (US EPA 2023). For the 15-day repeat exposure, there were severe histopathologic changes in the MucilAir nasal mock-treatment (air-only) VITROCELL chamber controls compared to incubator controls preventing any further analysis. The histopathological transitions in cellular morphology from pseudostratified columnar epithelium to squamous epithelium observed in the air only control in this study and previously with 1,3-DCP in MucilAir nasal cultures is also a hallmark of chemically induced cytotoxic responses in the respiratory tract. Histopathology assessments of 3D respiratory tract models used in ALI exposures can provide the linkage between to outcomes as part of the validation efforts of ALI use in regulatory toxicology. This report indicates that importance of histopathological assessments of incubator and mock-treatment (air-only) controls from each ALI exposure experiment along with exposed cell based model.

摘要

新方法学(NAMs)正被广泛用于减少、优化和替代毒理学研究中的动物使用。对于呼吸道毒理学而言,这包括使用气液界面(ALI)暴露的替代方法来取代传统的吸入研究。在先前使用1,3 - 二氯丙烯(1,3 - DCP)的研究中,对MucilAir鼻细胞培养模型进行为期5天、每天4小时的重复暴露,导致了剂量依赖性细胞毒性、谷胱甘肽耗竭、差异基因表达变化以及细胞形态从假复层柱状上皮向鳞状上皮的组织病理学转变。在本报告中,我们试图按照美国环境保护局(US EPA)最近的一项任务指令(US EPA 2023)所概述的,将这些研究扩展为使用MucilAir鼻培养物进行为期15天、每天4小时的1,3 - DCP暴露。对于为期15天的重复暴露,与培养箱对照相比,MucilAir鼻模拟处理(仅空气)VITROCELL腔室对照出现了严重的组织病理学变化,从而无法进行进一步分析。在本研究的仅空气对照以及先前在MucilAir鼻培养物中使用1,3 - DCP时观察到的细胞形态从假复层柱状上皮向鳞状上皮的组织病理学转变,也是呼吸道化学诱导细胞毒性反应的一个标志。在ALI暴露中使用的3D呼吸道模型的组织病理学评估可以作为ALI在监管毒理学中应用的验证工作的一部分,提供从暴露到结果的联系。本报告表明了对每个ALI暴露实验的培养箱和模拟处理(仅空气)对照以及基于暴露细胞的模型进行组织病理学评估的重要性。

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