Biology Department, Kenyon College, 302A College Park St., Gambier, OH 43022, United States.
Chem Biol Interact. 2010 Jan 5;183(1):202-11. doi: 10.1016/j.cbi.2009.09.017.
The aryl hydrocarbon receptor (AHR) mediates the toxic effects of environmental contaminants, such as 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). Frogs are very insensitive to TCDD toxicity, and AHRs from Xenopus laevis (African clawed frog) bind TCDD with >20-fold lower affinity than mouse AHR(b-1). Frog AHRs may nonetheless be highly responsive to structurally distinct compounds, especially putative endogenous ligands. We sought to determine the responsiveness of an X. laevis cell line, XLK-WG, to the candidate endogenous AHR ligand 6-formylindolo[3,2-b]carbazole (FICZ), a tryptophan photoproduct that exhibits high potency in mammalian systems. FICZ readily induced mRNAs for CYP1A6 and CYP1A7. Cells exposed to FICZ for 3h expressed up to 5-fold greater quantities of CYP1A6/7 mRNAs than those exposed for 24h, suggesting FICZ is metabolized following rapid enzyme induction. FICZ appeared more potent than TCDD. Following a 3-h exposure, the EC(50) for CYP1A6 mRNA induction by FICZ was approximately 6nM, while the TCDD response was greater than 174nM. These potencies were lower than those determined for mouse hepatoma cells (Hepa1c1c7; EC(50)= approximately 0.06nM each). The difference in ligand potency between cell lines was confirmed by induction of ethoxyresorufin-O-deethylase (EROD) activity. mRNA from XLK-WG cells treated with 100nM FICZ, 100nM TCDD, or vehicle was also analyzed on expression microarrays. FICZ altered the expression of 105 more transcripts than TCDD, and common targets were altered more dramatically by FICZ. Overall, these studies demonstrate that although FICZ is a less potent CYP1A inducer in frog cells than in mouse cells, the reduction is much less than for TCDD. Relative conservation of the FICZ response in a TCDD-insensitive species suggests its physiological importance as an AHR ligand.
芳香烃受体(AHR)介导环境污染物的毒性作用,如 2,3,7,8-四氯二苯并对二恶英(TCDD)。青蛙对 TCDD 的毒性非常不敏感,并且非洲爪蟾(非洲爪蟾)的 AHR 与小鼠 AHR(b-1)结合的亲和力低 20 倍以上。然而,青蛙 AHR 可能对结构不同的化合物高度敏感,特别是假定的内源性配体。我们试图确定 X. laevis 细胞系 XLK-WG 对候选内源性 AHR 配体 6-甲酰基吲哚并[3,2-b]咔唑(FICZ)的反应性,FICZ 是一种色氨酸光产物,在哺乳动物系统中具有高效力。FICZ 容易诱导 CYP1A6 和 CYP1A7 的 mRNA。与暴露 24 小时的细胞相比,暴露于 FICZ 3 小时的细胞表达的 CYP1A6/7 mRNA 多达 5 倍,这表明 FICZ 在快速酶诱导后被代谢。FICZ 似乎比 TCDD 更有效。在 3 小时暴露后,FICZ 诱导 CYP1A6 mRNA 的 EC(50)约为 6nM,而 TCDD 反应大于 174nM。这些效力低于确定的小鼠肝癌细胞(Hepa1c1c7;EC(50)= 每个约 0.06nM)。通过诱导乙氧基荧光素-O-脱乙基酶(EROD)活性,确认了细胞系之间配体效力的差异。用 100nM FICZ、100nM TCDD 或载体处理的 XLK-WG 细胞的 mRNA 也在表达微阵列上进行了分析。FICZ 改变了 105 个以上转录本的表达,而 TCDD 改变了更多常见的靶标。总体而言,这些研究表明,尽管 FICZ 是青蛙细胞中比小鼠细胞中较弱的 CYP1A 诱导剂,但减少量远小于 TCDD。在 TCDD 不敏感的物种中相对保留 FICZ 反应表明其作为 AHR 配体的生理重要性。