Retinoids repress Ah receptor CYP1A1 induction pathway through the SMRT corepressor

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 ad...

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Veröffentlicht in:Biochemical and biophysical research communications 2004-09, Vol.322 (2), p.551-556
Hauptverfasser: Fallone, Frédérique, Villard, Pierre-Henri, Sérée, Eric, Rimet, Odile, Nguyen, Quock Binh, Bourgarel-Rey, Véronique, Fouchier, Francis, Barra, Yves, Durand, Alain, Lacarelle, Bruno
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Sprache:eng
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Zusammenfassung: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.
ISSN:0006-291X
1090-2104
DOI:10.1016/j.bbrc.2004.07.153