Smad3–ATF3 signaling mediates TGF-β suppression of genes encoding Phase II detoxifying proteins

• Published in: Free radical biology & medicine 2005-02, Vol.38 (3), p.375-387
• Main Authors: Bakin, Andrei V., Stourman, Nina V., Sekhar, Konjeti R., Rinehart, Cammie, Yan, Xuexian, Meredith, Michael J., Arteaga, Carlos L., Freeman, Michael L.
• Format: Article
• Language: English
• Subjects: Activating Transcription Factor 3; Animals; ATF3; Catalase - drug effects; Catalase - genetics; Cell Line; DNA-Binding Proteins - drug effects; DNA-Binding Proteins - genetics; DNA-Binding Proteins - metabolism; Free radicals; Gene Expression Regulation - drug effects; Glutamate-Cysteine Ligase - drug effects; Glutamate-Cysteine Ligase - genetics; Glutathione; Glutathione - antagonists & inhibitors; Glutathione - biosynthesis; Glutathione Transferase - drug effects; Glutathione Transferase - genetics; Humans; Inactivation, Metabolic - genetics; Mice; Nrf2; Reactive Oxygen Species - metabolism; RNA, Messenger - drug effects; RNA, Messenger - metabolism; Signal Transduction - drug effects; Signal Transduction - physiology; Smad; Smad3 Protein; TGF-β; Trans-Activators - drug effects; Trans-Activators - genetics; Trans-Activators - metabolism; Transcription Factors - drug effects; Transcription Factors - metabolism; Transforming Growth Factor beta - metabolism; Transforming Growth Factor beta - pharmacology
• ISSN: 0891-5849; 1873-4596
• DOI: 10.1016/j.freeradbiomed.2004.10.033

This study provides evidence that in mammary epithelial cells the pluripotent cytokine TGF-β1 repressed expression of multiple genes involved in Phase II detoxification. GCLC, the gene that encodes the catalytic subunit of the enzyme glutamate cysteine ligase, the rate-limiting enzyme in the biosynthesis of glutathione, was used as a molecular surrogate for investigating the mechanisms by which TGF-β suppressed Phase II gene expression. TGF-β was found to suppress luciferase reporter activity mediated by the human GCLC proximal promoter, as well as reporter activity mediated by the GCLC antioxidant response element, ARE4. TGF-β downregulated expression of endogenous GCLC mRNA and GCLC protein. TGF-β suppression of the Phase II genes correlated with a decrease in cellular glutathione and an increase in cellular reactive oxygen species. Ectopic expression of constitutively active Smad3E was sufficient to inhibit both reporters in the absence of TGF-β, whereas dominant negative Smad3A blocked TGF-β suppression. Smad3E suppressed Nrf2-mediated activation of the GCLC reporter. We demonstrate that TGF-β increased ATF3 protein levels, as did transient overexpression of Smad3E. Ectopic expression of ATF3 was sufficient to suppress the GCLC reporter activity, as well as endogenous GCLC expression. These results demonstrate that Smad3–ATF3 signaling mediates TGF-β repression of ARE-dependent Phase II gene expression and potentially provide critical insight into mechanisms underlying TGF-β1 function in carcinogenesis, tissue repair, and fibrosis.