A Comparative Study of Different In Vitro Lung Cell Culture Systems to Assess the Most Beneficial Tool for Screening the Potential Adverse Effects of Carbon Nanotubes

被引:52
作者
Clift, Martin J. D. [1 ]
Endes, Carola [1 ]
Vanhecke, Dimitri [1 ]
Wick, Peter [2 ]
Gehr, Peter [3 ]
Schins, Roel P. F. [4 ]
Petri-Fink, Alke [1 ,5 ]
Rothen-Rutishauser, Barbara [1 ,6 ]
机构
[1] Univ Fribourg, Bionanomat Adolphe Merkle Inst, CH-1723 Fribourg, Switzerland
[2] Empa, Swiss Fed Labs Mat Sci & Technol, Mat Biol Interact Lab, CH-9014 St Gallen, Switzerland
[3] Univ Bern, Inst Anat, CH-3012 Bern, Switzerland
[4] Univ Dusseldorf, Inst Umweltmed Forsch IUF, D-40225 Dusseldorf, Germany
[5] Univ Fribourg, Dept Chem, CH-1700 Fribourg, Switzerland
[6] Univ Hosp Bern, CH-3010 Bern, Switzerland
基金
瑞士国家科学基金会;
关键词
in vitro lung systems; carbon nanotubes; nanotoxicology; oxidative stress; inflammation; risk assessment; OXIDATIVE STRESS; NANOPARTICLES; INFLAMMATION; MACROPHAGES; TOXICITY; INDUCE; MODEL; NANOTOXICOLOGY; DISPERSION; TOXICOLOGY;
D O I
10.1093/toxsci/kft216
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
To determine the potential inhalatory risk posed by carbon nanotubes (CNTs), a tier-based approach beginning with an in vitro assessment must be adopted. The purpose of this study therefore was to compare 4 commonly used in vitro systems of the human lung (human blood monocyte-derived macrophages [MDM] and monocyte-derived dendritic cells [MDDC], 16HBE14o- epithelial cells, and a sophisticated triple cell co-culture model [TCC-C]) via assessment of the biological impact of different CNTs (single-walled CNTs [SWCNTs] and multiwalled CNTs [MWCNTs]) over 24h. No significant cytotoxicity was observed with any of the cell types tested, although a significant (p < .05), dose-dependent increase in tumor necrosis factor (TNF)- following SWCNT and MWCNT exposure at concentrations up to 0.02mg/ml to MDM, MDDC, and the TCC-C was found. The concentration of TNF- released by the MDM and MDDC was significantly higher (p < .05) than the TCC-C. Significant increases (p < .05) in interleukin (IL)-8 were also found for both 16HBE14o- epithelial cells and the TCC-C after SWCNTs and MWCNTs exposure up to 0.02mg/ml. The TCC-C, however, elicited a significantly (p < .05) higher IL-8 release than the epithelial cells. The oxidative potential of both SWCNTs and MWCNTs (0.0050.02mg/ml) measured by reduced glutathione (GSH) content showed a significant difference (p < .05) between each monoculture and the TCC-C. It was concluded that because only the co-culture system could assess each endpoint adequately, that, in comparison with monoculture systems, multicellular systems that take into consideration important cell type-to-cell type interactions could be used as predictive in vitro screening tools for determining the potential deleterious effects associated with CNTs.
引用
收藏
页码:55 / 64
页数:10
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