Genomic signatures and dose-dependent transitions in nasal epithelial responses to inhaled formaldehyde in the rat
- PMID: 18499655
- DOI: 10.1093/toxsci/kfn097
Genomic signatures and dose-dependent transitions in nasal epithelial responses to inhaled formaldehyde in the rat
Abstract
Repeated and acute exposure studies assessed time and concentration-dependencies of nasal responses to formaldehyde. Exposures were to 0, 0.7, 2, and 6 ppm for 6 h/day, 5 days/week for up to 3 weeks. Neither cell proliferation nor histopathology was observed at 0.7 ppm. At 6 ppm, cell proliferation increased at the end of the first week (day 5), but not at the end of week 3 (day 15). Squamous metaplasia occurred at day 5; epithelial hyperplasia occurred at both day 5 and day 15. In microarray studies, no genes were altered at 0.7 ppm. At 2 ppm, 15 genes were changed on day 5; only half of them were changed at 6 ppm. No genes were changed significantly at 2 ppm at day 15. The pattern of gene changes at 2 and 6 ppm, with transient squamous metaplasia at day 5, indicated tissue adaptation and reduced tissue sensitivity by day 15. The acute study included an additional concentration (15 ppm) and an instillation group (40 microl, 400 mM per nostril). Three times more genes were affected by instillation than inhalation. U-shaped dose responses were noted in the acute study for many genes that were also altered at 2 ppm on day 5. On the basis of cellular component gene ontology benchmark dose analysis, the most sensitive changes were for genes were associated with extracellular components and plasma membrane. With formaldehyde, there are temporal and concentration-dependent transitions in epithelial responses and genomic signatures between 0.7 and 6 ppm. Low concentrations primarily affect extracellular matrix or external plasma membrane portions of the epithelium.
Comment in
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Gene expression, dose-response, and phenotypic anchoring: applications for toxicogenomics in risk assessment.Toxicol Sci. 2008 Oct;105(2):233-4. doi: 10.1093/toxsci/kfn138. Epub 2008 Aug 6. Toxicol Sci. 2008. PMID: 18684776 No abstract available.
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