DeGroot Danica E, Franks Diana G, Higa Tatsuo, Tanaka Junichi, Hahn Mark E, Denison Michael S
†Department of Environmental Toxicology, University of California, Davis, California 95616, United States.
‡Department of Biology and the Woods Hole Center for Oceans and Human Health, Woods Hole Oceanographic Institution, Woods Hole, Massachusetts 02543, United States.
Chem Res Toxicol. 2015 Jun 15;28(6):1176-85. doi: 10.1021/acs.chemrestox.5b00003. Epub 2015 Jun 2.
The aryl hydrocarbon receptor (AhR) is a ligand-dependent transcription factor that mediates the toxic and biological effects of structurally diverse chemicals, including the environmental contaminant 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD). As part of a larger effort to identify the full spectrum of chemicals that can bind to and activate the AhR, we have examined the ability of several naturally occurring marine-derived brominated indoles and brominated (methylthio)indoles (collectively referred to as brominated indoles) to bind to the AhR and stimulate AhR-dependent gene expression. Incubation of mouse, rat, and guinea pig recombinant cell lines containing a stably transfected AhR-responsive luciferase reporter gene with eight brominated indoles revealed that all compounds stimulated luciferase reporter gene activity, although some species-specific differences were observed. All compounds induced significantly more luciferase activity when incubated with cells for 4 h as compared to 24 h, demonstrating that these compounds are transient activators of the AhR signaling pathway. Three of the brominated indoles induced CYP1A1 mRNA in human HepG2 cells in vitro and Cyp1a mRNA in zebrafish embryos in vivo. The identification of the brominated indoles as direct ligands and activators/agonists of the AhR was confirmed by their ability to compete with [(3)H]TCDD for binding to the AhR and to stimulate AhR transformation and DNA binding in vitro. Taken together, these results indicate that marine-derived brominated indoles are members of a new class of naturally occurring AhR agonists.
芳烃受体(AhR)是一种依赖配体的转录因子,可介导结构多样的化学物质的毒性和生物学效应,包括环境污染物2,3,7,8-四氯二苯并对二恶英(TCDD)。作为确定能够结合并激活AhR的化学物质全谱的更大努力的一部分,我们研究了几种天然存在的海洋来源的溴化吲哚和溴化(甲硫基)吲哚(统称为溴化吲哚)与AhR结合并刺激AhR依赖性基因表达的能力。用八种溴化吲哚孵育含有稳定转染的AhR反应性荧光素酶报告基因的小鼠、大鼠和豚鼠重组细胞系,结果显示所有化合物均刺激了荧光素酶报告基因活性,尽管观察到了一些物种特异性差异。与孵育24小时相比,所有化合物与细胞孵育4小时时诱导的荧光素酶活性明显更高,这表明这些化合物是AhR信号通路的瞬时激活剂。三种溴化吲哚在体外可诱导人HepG2细胞中的CYP1A1 mRNA,在体内可诱导斑马鱼胚胎中的Cyp1a mRNA。溴化吲哚作为AhR的直接配体和激活剂/激动剂的身份通过它们与[³H]TCDD竞争结合AhR以及在体外刺激AhR转化和DNA结合的能力得到了证实。综上所述,这些结果表明海洋来源的溴化吲哚是一类新型天然AhR激动剂的成员。