Human primary bronchial epithelial cells respond differently to titanium dioxide nanoparticles than the lung epithelial cell lines A549 and BEAS-2B

被引:60
作者
Ekstrand-Hammarstrom, Barbro [1 ]
Akfur, Christine M. [1 ]
Andersson, Per Ola [1 ]
Lejon, Christian [1 ]
Osterlund, Lars [1 ,2 ]
Bucht, Anders [1 ,3 ]
机构
[1] Swedish Def Res Agcy, Div CBRN Def & Secur, Umea, Sweden
[2] Uppsala Univ, Angstrom Lab, Dept Engn Sci, Uppsala, Sweden
[3] Umea Univ, Dept Publ Hlth & Clin Med, Umea, Sweden
关键词
TiO2; nanoparticles; normal human bronchial epithelial cells; rutile; anatase; inflammation; INCREASED PULMONARY TOXICITY; OXIDATIVE STRESS; SURFACE-AREA; ULTRAFINE PARTICLES; FINE PARTICLES; RUTILE TIO2; IN-VITRO; KAPPA-B; KINASE; CYTOTOXICITY;
D O I
10.3109/17435390.2011.598245
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We have compared the cellular uptake and responses of five preparations of nanocrystalline titanium dioxide (TiO2) between normal human bronchial epithelial (NHBE) cells and epithelial cell lines (A549 and BEAS-2B). The P25 nanoparticles, containing both anatase and rutile modifications, induced reactive oxygen species (ROS) and secretion of the neutrophil chemoattractant IL-8 in all three cell types used. Pure anatase and rutile particles provoked differential IL-8 response in A549 and no response in BEAS-2B cells despite similar formation of ROS. The pure TiO2 modifications also provoked release of the inflammatory mediators: IL-6, G-CSF and VEGF, in NHBE cells but not in the two cell lines. We conclude that the responsiveness of lung epithelial cells is strongly dependent on both the physicochemical properties of TiO2 nanoparticles and the type of responder cells. The differential pro-inflammatory responsiveness of primary lung epithelial cells compared with immortalized cell lines should be considered in the assessment of adverse reactions to inhaled nanoparticles.
引用
收藏
页码:623 / 634
页数:12
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