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在基于原代细胞的三维气液界面鼻组织模型中评估打印机碳粉颗粒的细胞毒性和基因毒性潜力。

Evaluation of the cytotoxic and genotoxic potential of printer toner particles in a 3D air-liquid interface, primary cell-based nasal tissue model.

作者信息

Meyer Till Jasper, Tekin Nursen, Hense Peter, Ehret-Kasemo Totta, Lodes Nina, Stöth Manuel, Ickrath Pascal, Gehrke Thomas, Hagen Rudolf, Dembski Sofia, Peer Michael, Steinke Maria R, Scherzad Agmal, Hackenberg Stephan

机构信息

University Hospital Würzburg, Department of Oto-Rhino-Laryngology, Plastic, Aesthetic & Reconstructive Head and Neck Surgery, Josef-Schneider-Straße 11, 97080 Würzburg, Germany.

University Hospital Würzburg, Department of Oto-Rhino-Laryngology, Plastic, Aesthetic & Reconstructive Head and Neck Surgery, Josef-Schneider-Straße 11, 97080 Würzburg, Germany.

出版信息

Toxicol Lett. 2023 Apr 15;379:1-10. doi: 10.1016/j.toxlet.2023.03.004. Epub 2023 Mar 11.

Abstract

Printer toner particles (TPs) are a common, potentially hazardous substance, with an unclear toxicological impact on the respiratory mucosa. Most of the airways surface is covered by a ciliated respiratory mucosa, therefore appropriate tissue models of the respiratory epithelium with a high in vivo correlation are necessary for in vitro evaluation of airborne pollutants toxicology and the impact on the functional integrity. The aim of this study is the evaluation of TPs toxicology in a human primary cell-based air-liquid-interface (ALI) model of respiratory mucosa. The TPs were analyzed and characterized by scanning electron microscopy, pyrolysis and X-ray fluorescence spectrometry. ALI models of 10 patients were created using the epithelial cells and fibroblasts derived from nasal mucosa samples. TPs were applied to the ALI models via a modified Vitrocell® cloud and submerged in the dosing 0.89 - 892.96 µg/ cm. Particle exposure and intracellular distribution were evaluated by electron microscopy. The MTT assay and the comet assay were used to investigate cytotoxicity and genotoxicity, respectively. The used TPs showed an average particle size of 3 - 8 µm. Mainly carbon, hydrogen, silicon, nitrogen, tin, benzene and benzene derivates were detected as chemical ingredients. By histomorphology and electron microscopy we observed the development of a highly functional, pseudostratified epithelium with a continuous layer of cilia. Using electron microscopy, TPs could be detected on the cilia surface and also intracellularly. Cytotoxicity was detected from 9 µg/ cm and higher, but no genotoxicity after ALI and submerged exposure. The ALI with primary nasal cells represents a highly functional model of the respiratory epithelium in terms of histomorphology and mucociliary differentiation. The toxicological results indicate a weak TP-concentration-dependent cytotoxicity. AVAILABILITY OF DATA AND MATERIALS: The datasets used and analysed during the current study are available from the corresponding author on reasonable request.

摘要

打印机碳粉颗粒(TPs)是一种常见的潜在有害物质,对呼吸道黏膜的毒理学影响尚不清楚。大部分气道表面覆盖着纤毛呼吸黏膜,因此,具有高度体内相关性的合适的呼吸道上皮组织模型对于体外评估空气传播污染物的毒理学及其对功能完整性的影响是必要的。本研究的目的是在基于人原代细胞的呼吸黏膜气液界面(ALI)模型中评估TPs的毒理学。通过扫描电子显微镜、热解和X射线荧光光谱法对TPs进行分析和表征。使用源自鼻黏膜样本的上皮细胞和成纤维细胞创建了10名患者的ALI模型。通过改良的Vitrocell®云雾装置将TPs应用于ALI模型,并以0.89 - 892.96 μg/cm的剂量进行浸没给药。通过电子显微镜评估颗粒暴露和细胞内分布。分别使用MTT法和彗星试验研究细胞毒性和遗传毒性。所使用的TPs平均粒径为3 - 8 µm。检测到的化学成分主要有碳、氢、硅、氮、锡、苯和苯衍生物。通过组织形态学和电子显微镜观察,我们发现形成了具有连续纤毛层的高度功能性假复层上皮。使用电子显微镜,可以在纤毛表面以及细胞内检测到TPs。在9 μg/cm及更高剂量时检测到细胞毒性,但在ALI和浸没暴露后未检测到遗传毒性。就组织形态学和黏液纤毛分化而言,具有原代鼻细胞的ALI代表了呼吸道上皮的高度功能性模型。毒理学结果表明存在较弱的TP浓度依赖性细胞毒性。数据和材料的可用性:在当前研究中使用和分析的数据集可应相应作者的合理要求提供。

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