Retinoids repress Ah receptor CYP1A1 induction pathway through the SMRT corepressor

被引:35
作者
Fallone, F
Villard, PH
Sérée, E
Rimet, O
Nguyen, QB
Bourgarel-Rey, W
Fouchier, F
Barra, Y
Durand, A
Lacarelle, B
机构
[1] Univ Mediterranee, Fac Pharm, CNRS, FRE 2737, F-13385 Marseille 05, France
[2] Univ Mediterranee, Fac Pharm, Toxicol Lab, F-13385 Marseille 05, France
关键词
CYP1A1; regulation; repression; aryl hydrocarbon receptor; ligand; PAH; retinoids; SMRT; corepressor; interaction; Caco-2cells;
D O I
10.1016/j.bbrc.2004.07.153
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
CYP1A1 isoform is mainly regulated by the transcription factor AhR and to a lesser extent by the nuclear receptor RAR. The effect of a coexposure with 3MC, a AhR ligand, and RA, a RAR ligand, which are, respectively, strong and weak CYP1A1 inducers, is poorly known. We showed in Caco-2 cells that addition of RA significantly decreased 3MC-induced CYP1A1 expression by -55% for mRNA level and -30% for promoter and enzymatic activities. We further showed that RA decreased AhR protein level. Moreover, a physical interaction between AhR and the RAR-corepressor SMRT has been described in vitro. Using the corepressor inhibitor TSA, transfected-cells with SMRT cDNA, and coimmunoprecipitation experiments, we demonstrated that RA addition repressed AhR function through a marked AhR/SMRT physical interaction. This interaction explains the decrease of 3MC-induced CYP1A1 expression. This new mechanism involving the repression of AhR-induced CYP1A1 expression by retinoids allows better knowledge of the CYP1A1 regulation. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:551 / 556
页数:6
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