Abstract
Flavin-containing monooxygenases (FMOs) are important in detoxication but generally are considered not to be inducible by xenobiotics. Our recent microarray studies revealed induction of FMO2 and FMO3 mRNAs by 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) in liver of mice with wild-type aryl hydrocarbon receptor (AHR) but not in Ahr-null mice. The aim of the present study was to delineate mechanisms of FMO regulation. In adult male mice, basal FMO3 mRNA is low but was induced 6-fold at 4 h and 6000-fold at 24 h. The ED50 was approximately 1 μg/kg for FMO2 and FMO3, similar to that for the classic AHR-regulated gene, Cyp1a1. In adult female mice basal FMO3 mRNA is high and was not induced at 4 h but was elevated 8-fold at 24 h. FMO5 mRNA was significantly down-regulated by TCDD in both male and female adult mice. Juvenile mice show no sex difference in response to TCDD; FMO3 was induced 4 to 6-fold by TCDD in both sexes. Chromatin immunoprecipitation demonstrated recruitment of AHR and aryl hydrocarbon nuclear translocator proteins to Fmo3 regulatory regions, suggesting that induction by TCDD is a primary AHR-mediated event. Although FMO2 and FMO3 mRNAs were highly induced by TCDD in adult males, overall FMO catalytic activity increased only modestly. In contrast to the striking up-regulation of FMO2 and FMO3 in mouse liver, TCDD has little effect on FMO mRNA in rat liver. However, FMO2 and FMO3 mRNAs were highly induced in transgenic mice that express wild-type rat AHR, indicating that lack of induction in rat is not due to an incompetent AHR in this species.
Footnotes
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This work was supported by Grant MOP-57903 from the Canadian Institutes of Health (to A.B.O.) and Grant 123345 from the Academy of Finland (to R.P.).
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Article, publication date, and citation information can be found at http://dmd.aspetjournals.org.
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doi:10.1124/dmd.108.023457.
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ABBREVIATIONS: FMO, flavin-containing monooxygenase; TCDD, 2,3,7,8-tetrachlorodibenzo-p-dioxin (dioxin); AHR, aryl hydrocarbon receptor; AHRE, aryl hydrocarbon response elements; DTNB, 5,5′-dithiobis(2-nitrobenzoate); MMI, methimazole; DTT, dithiothreitol; PCR, polymerase chain reaction; ChIP, chromatin immunoprecipitation; RT, reverse transcription; miRNA, microRNA; CT, threshold cycle.
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↵ The online version of this article (available at http://dmd.aspetjournals.org) contains supplemental material.
- Received July 18, 2008.
- Accepted August 29, 2008.
- The American Society for Pharmacology and Experimental Therapeutics
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