2020
DOI: 10.3791/61210
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An Air-liquid Interface Bronchial Epithelial Model for Realistic, Repeated Inhalation Exposure to Airborne Particles for Toxicity Testing

Abstract: 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 particle… Show more

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Cited by 34 publications
(42 citation statements)
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References 23 publications
(32 reference statements)
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“…Primary cells, however, differ from batchto-batch and are more challenging to maintain than cell lines. This represents a significant disadvantage when conducting high throughput screening and toxicological testing [79]. Published studies have shown consistent evidence that different types of human bronchial cell lines (BEAS-2B; Calu-3; HFL-1; H292) and primary human bronchial epithelial cells display different cellular toxicity profiles following in vitro exposures to tobacco-related products or their constituents [48; 80].…”
Section: Discussionmentioning
confidence: 99%
“…Primary cells, however, differ from batchto-batch and are more challenging to maintain than cell lines. This represents a significant disadvantage when conducting high throughput screening and toxicological testing [79]. Published studies have shown consistent evidence that different types of human bronchial cell lines (BEAS-2B; Calu-3; HFL-1; H292) and primary human bronchial epithelial cells display different cellular toxicity profiles following in vitro exposures to tobacco-related products or their constituents [48; 80].…”
Section: Discussionmentioning
confidence: 99%
“…[ 38 ] These in vitro systems are particularly advantageous for lung cell models because they allow for apical exposure of epithelial cells to air, thus more closely representing the in vivo situation for epithelial cells in the respiratory tract. [ 67 ]…”
Section: Discussionmentioning
confidence: 99%
“…Calu-3 cells were grown in air-liquid interface as described elsewhere (25). Briefly, Calu-3 cells were seeded at 30,000 on 3 μm pore size transwell inserts (Corning - 3415).…”
Section: Methodsmentioning
confidence: 99%