Sawaya Rana M, Riddick David S
Department of Pharmacology and Toxicology, Medical Sciences Building, University of Toronto, Toronto, ON, Canada.
Drug Metab Dispos. 2008 Sep;36(9):1803-11. doi: 10.1124/dmd.108.020966. Epub 2008 Jun 4.
Aromatic hydrocarbons such as 3-methylcholanthrene (MC) elicit toxic and adaptive responses through the aryl hydrocarbon receptor (AHR). Aromatic hydrocarbons act via an unknown mechanism to suppress the transcription of CYP2C11, a growth hormone-regulated gene encoding the male-specific rat hepatic cytochrome P450 2C11. We hypothesize that suppression of CYP2C11 by aromatic hydrocarbons is mediated by the gene's promoter and 5'-flank. Using hydrodynamics-based injections to deliver plasmid DNA to the liver of live rats, we studied the MC responsiveness of luciferase constructs containing 10.1, 5.6, and 2.4 kilobases (kb) of the CYP2C11 5'-flank. MC suppressed CYP2C11-luciferase activity of the 10.1- and 5.6-kb constructs to less than 50% of vehicle levels by 24 and 72 h. Luciferase activity of the 2.4-kb CYP2C11 construct was decreased to 63% of vehicle levels 24 h after MC treatment, but no suppression was detected by 72 h. Negative regulatory element(s) responsible for CYP2C11 reporter suppression by MC exist in the proximal 2.4 kb of the 5'-flank; however, additional cis-acting elements located between -5.6 and -2.4 kb mediate persistent reporter suppression. As a positive control for AHR activation, MC dramatically induced the luciferase activity of a Cyp1a1-driven luciferase plasmid under AHR control. Modulation of reporter gene activity by MC was accompanied by induction of endogenous CYP1A1 and suppression of endogenous CYP2C11 mRNA/protein. This is the first demonstration of aromatic hydrocarbon-mediated suppression of a CYP2C11-luciferase construct, and this finding suggests that the 5'-flanking region and promoter mediate down-regulation of this gene in the intact rat.
诸如3-甲基胆蒽(MC)之类的芳香烃通过芳烃受体(AHR)引发毒性和适应性反应。芳香烃通过未知机制抑制CYP2C11的转录,CYP2C11是一种受生长激素调节的基因,编码雄性特异性大鼠肝脏细胞色素P450 2C11。我们假设芳香烃对CYP2C11的抑制作用是由该基因的启动子和5'侧翼介导的。利用基于流体动力学的注射方法将质粒DNA导入活大鼠的肝脏,我们研究了含有CYP2C11 5'侧翼10.1、5.6和2.4千碱基(kb)的荧光素酶构建体对MC的反应性。在24小时和72小时时,MC将10.1 kb和5.6 kb构建体的CYP2C11-荧光素酶活性抑制至低于载体水平的50%。在MC处理24小时后,2.4 kb CYP2C11构建体的荧光素酶活性降至载体水平的63%,但在72小时时未检测到抑制作用。负责MC抑制CYP2C11报告基因的负调控元件存在于5'侧翼的近端2.4 kb中;然而,位于-5.6和-2.4 kb之间的其他顺式作用元件介导了持续的报告基因抑制。作为AHR激活的阳性对照,MC显著诱导了AHR控制下的Cyp1a1驱动的荧光素酶质粒的荧光素酶活性。MC对报告基因活性的调节伴随着内源性CYP1A1的诱导和内源性CYP2C11 mRNA/蛋白的抑制。这是首次证明芳香烃介导的对CYP2C11-荧光素酶构建体的抑制作用,这一发现表明5'侧翼区域和启动子在完整大鼠中介导了该基因的下调。