An Air-liquid Interface Bronchial Epithelial Model for Realistic, Repeated Inhalation Exposure to Airborne Particles for Toxicity Testing

被引:39
作者
Braakhuis, Hedwig M. [1 ]
He, Ruiwen [1 ,2 ]
Vandebriel, Rob J. [1 ]
Gremmer, Eric R. [1 ]
Zwart, Edwin [1 ]
Vermeulen, Jolanda P. [1 ]
Fokkens, Paul [1 ]
Boere, John [1 ]
Gosens, Ilse [1 ]
Cassee, Flemming R. [1 ,2 ]
机构
[1] Natl Inst Publ Hlth & Environm RIVM, Bilthoven, Netherlands
[2] Inst Risk Assessment Sci IRAS, Utrecht, Netherlands
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2020年 / 159期
关键词
Biology; Issue; 159; air-liquid interface; bronchial model; inhalation exposure; toxicity; realistic exposure; in vitro; nanomaterials; IN-VITRO; AMORPHOUS SILICAS; LUNG; AEROSOLS; CELLS; RATS;
D O I
10.3791/61210
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
For toxicity testing of airborne particles, air-liquid interface (ALI) exposure systems have been developed for in vitro tests in order to mimic realistic exposure conditions. This puts specific demands on the cell culture models. Many cell types are negatively affected by exposure to air (e.g., drying out) and only remain viable for a few days. This limits the exposure conditions that can be used in these models: usually relatively high concentrations are applied as a cloud (i.e., droplets containing particles, which settle down rapidly) within a short period of time. Such experimental conditions do not reflect realistic long-term exposure to low concentrations of particles. To overcome these limitations the use of a human bronchial epithelial cell line, Calu-3 was investigated. These cells can be cultured at ALI conditions for several weeks while retaining a healthy morphology and a stable monolayer with tight junctions. In addition, this bronchial model is suitable for testing the effects of repeated exposures to low, realistic concentrations of airborne particles using an ALI exposure system. This system uses a continuous airflow in contrast to other ALI exposure systems that use a single nebulization producing a cloud. Therefore, the continuous flow system is suitable for repeated and prolonged exposure to airborne particles while continuously monitoring the particle characteristics, exposure concentration, and delivered dose. Taken together, this bronchial model, in combination with the continuous flow exposure system, is able to mimic realistic, repeated inhalation exposure conditions that can be used for toxicity testing.
引用
收藏
页数:10
相关论文
共 33 条
[1]   Five-day inhalation toxicity study of three types of synthetic amorphous silicas in Wistar rats and post-exposure evaluations for up to 3 months [J].
Arts, Josje H. E. ;
Muijser, Hans ;
Duistermaat, Evert ;
Junker, Karin ;
Kuper, C. Frieke .
FOOD AND CHEMICAL TOXICOLOGY, 2007, 45 (10) :1856-1867
[2]   An updated review of the genotoxicity of respirable crystalline silica [J].
Borm, Paul J. A. ;
Fowler, Paul ;
Kirkland, David .
PARTICLE AND FIBRE TOXICOLOGY, 2018, 15
[3]   The carcinogenic action of crystalline silica: A review of the evidence supporting secondary inflammation-driven genotoxicity as a principal mechanism [J].
Borm, Paul J. A. ;
Tran, Lang ;
Donaldson, Ken .
CRITICAL REVIEWS IN TOXICOLOGY, 2011, 41 (09) :756-770
[4]   Progress and future of in vitro models to study translocation of nanoparticles [J].
Braakhuis, Hedwig M. ;
Kloet, Samantha K. ;
Kezic, Sanja ;
Kuper, Frieke ;
Park, Margriet V. D. Z. ;
Bellmann, Susann ;
van der Zande, Meike ;
Le Gac, Severine ;
Krystek, Petra ;
Peters, Ruud J. B. ;
Rietjens, Ivonne M. C. M. ;
Bouwmeester, Hans .
ARCHIVES OF TOXICOLOGY, 2015, 89 (09) :1469-1495
[5]   Inflammatory mediators induced by intratracheal instillation of ultrafine amorphous silica particles [J].
Cho, Wan-Seob ;
Choi, Mina ;
Han, Beom Seok ;
Cho, Minjung ;
Oh, JaeHo ;
Park, Kidae ;
Kim, Sung Jun ;
Kim, Seung Hee ;
Jeong, Jayoung .
TOXICOLOGY LETTERS, 2007, 175 (1-3) :24-33
[6]   PULMONARY RESPONSE TO INHALED SILICA OR TITANIUM-DIOXIDE [J].
DRISCOLL, KE ;
LINDENSCHMIDT, RC ;
MAURER, JK ;
PERKINS, L ;
PERKINS, M ;
HIGGINS, J .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1991, 111 (02) :201-210
[7]   An in vitro testing strategy towards mimicking the inhalation of high aspect ratio nanoparticles [J].
Endes, Carola ;
Schmid, Otmar ;
Kinnear, Calum ;
Mueller, Silvana ;
Camarero-Espinosa, Sandra ;
Vanhecke, Dimitri ;
Foster, E. Johan ;
Petri-Fink, Alke ;
Rothen-Rutishauser, Barbara ;
Weder, Christoph ;
Clift, Martin J. D. .
PARTICLE AND FIBRE TOXICOLOGY, 2014, 11
[8]   Evaluating Adverse Effects of Inhaled Nanoparticles by Realistic In Vitro Technology [J].
Geiser, Marianne ;
Jeannet, Natalie ;
Fierz, Martin ;
Burtscher, Heinz .
NANOMATERIALS, 2017, 7 (02)
[9]   Culture of Calu-3 cells at the air interface provides a representative model of the airway epithelial barrier [J].
Grainger, Christopher I. ;
Greenwell, Leona L. ;
Lockley, David J. ;
Martin, Gary P. ;
Forbes, Ben .
PHARMACEUTICAL RESEARCH, 2006, 23 (07) :1482-1490
[10]   Evaluation of the Calu-3 cell line as a model of in vitro respiratory syncytial virus infection [J].
Harcourt, Jennifer L. ;
Caidi, Hayat ;
Anderson, Larry J. ;
Haynes, Lia M. .
JOURNAL OF VIROLOGICAL METHODS, 2011, 174 (1-2) :144-149