Monteiro Patricia, Gilot David, Le Ferrec Eric, Lecureur Valérie, N'diaye Monique, Le Vee Marc, Podechard Normand, Pouponnot Celio, Fardel Olivier
UMR-INSERM U620, Equipe Toxicity of Polycyclic Aromatic Hydrocarbons, IFR140, Université de Rennes 1, Faculté des Sciences Pharmaceutiques et Biologiques, 2 Avenue du Professeur Léon Bernard, Rennes Cedex, France.
Biochem Biophys Res Commun. 2007 Jun 29;358(2):442-8. doi: 10.1016/j.bbrc.2007.04.111. Epub 2007 Apr 26.
In order to identify molecular targets of environmental polycyclic aromatic hydrocarbons (PAHs), we have analysed regulation of integrin (ITG) expression in PAH-exposed human macrophages. Among ITG subunits, beta7 ITG was found to be markedly up-regulated at both mRNA and protein levels in response to the prototypical PAH benzo(a)pyrene (BP). Knock-down of the transcription factor c-maf, known to control beta7 ITG expression, markedly impaired BP-mediated beta7 ITG induction. Moreover, chromatin immunoprecipitation and electrophoretic mobility shift assays showed BP-triggered binding of c-maf to a specific maf-responsive element found in beta7 ITG promoter. Such a binding, and also beta7 ITG induction, were however abolished in response to chemical inhibition of the aryl hydrocarbon receptor (AhR), to which PAHs bind. Taken together, these data establish beta7 ITG as a new molecular target of PAHs, whose up-regulation by these environmental contaminants most likely requires activation of co-operative pathways involving both AhR and c-maf.
为了确定环境多环芳烃(PAHs)的分子靶点,我们分析了PAH暴露的人类巨噬细胞中整合素(ITG)表达的调控情况。在ITG亚基中,发现原型PAH苯并(a)芘(BP)可使β7 ITG在mRNA和蛋白质水平均显著上调。已知转录因子c-maf可控制β7 ITG的表达,敲低该转录因子会显著削弱BP介导的β7 ITG诱导作用。此外,染色质免疫沉淀和电泳迁移率变动分析表明,BP可促使c-maf与β7 ITG启动子中发现的特定maf反应元件结合。然而,在对PAHs所结合的芳烃受体(AhR)进行化学抑制后,这种结合以及β7 ITG的诱导作用均被消除。综上所述,这些数据确定β7 ITG是PAHs的一个新分子靶点,这些环境污染物对其上调作用很可能需要激活涉及AhR和c-maf的协同途径。