Impact of the composition of combustion generated fine particles on epithelial cell toxicity: influences of metals on metabolism

被引:39
作者
Okeson, CD
Riley, MR
Fernandez, A
Wendt, JOL
机构
[1] Univ Arizona, Dept Agr & Biosyst Engn, Tucson, AZ 85721 USA
[2] Univ Arizona, Dept Chem & Environm Engn, Tucson, AZ 85721 USA
关键词
epithelial cell culture; PM toxicity; cell metabolism; cell growth inhibition;
D O I
10.1016/S0045-6535(02)00721-X
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Inhaled airborne particulate matter (PM) represents a potentially significant health hazard to humans. Exposure to PM strongly correlates with pulmonary inflammation and incidences of severe respiratory distress, including increased hospital admissions for breathing disorders, asthma, emphysema, and chronic bronchitis. PM generated from the combustion of fuel oils and coals contain a number of water-soluble transition metals including Fe, V, and Zn. We have evaluated the impact of PM types with varying composition collected from the combustion of oils and coals on the health and metabolism of lung cell cultures. Three colorimetric assays (sulforhodamine B (SRB), Janus green, and MTT) have been adapted to quantify the impact of PM on rat lung alveolar type 11 epithelial cells (RLE-6TN cells). The PM toxicity metrics evaluated were inhibition of cell proliferation (SRB and Janus green) and inhibition of cellular metabolism (MTT). Cell proliferation is inhibited in a consistent dose-dependent manner by PM concentrations from 25 to 250 mug/ml. At a level of 100 mug/ml, oil-derived PM diminishes cell metabolism by as much as 40% relative to controls; the degree of inhibition is strongly dependent on PM particle size and metal content. Conversely, coal-derived PM at the same dosage diminishes cell metabolism by no more than 20% relative to controls. All three assays provide highly repeatable results and consistent toxicity rankings of the PMs evaluated. Overall, metabolic inhibition as measured by the MTT assay was deemed the most appropriate metric for PM toxicity, primarily due to its applicability with in vivo-like confluent cell monolayers. (C) 2003 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1121 / 1128
页数:8
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