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Expression of stress-response ATF3 is mediated by Nrf2 in astrocytes

Cited 35 time in Web of Science Cited 36 time in Scopus
Authors
Kim, Kyu-Han; Jeong, Jae-Yeon; Surh, Young-Joon; Kim, Kyu-Won
Issue Date
2010-01
Citation
Nucleic Acids Research, Vol.38 No.1, pp.48-59
Abstract
Activating Transcription Factor 3 (ATF3), a member of the ATF/CREB family, is induced rapidly by various stresses. Its induction mechanism and role in response to changes in cellular redox status, however, have not been elucidated. Here, we found that NF-E2-related factor 2 (Nrf2), a transcription factor known to bind to antioxidant response element (ARE) in promoters, transcriptionally upregulated ATF3 expression in astrocytes. Treatment with Nrf2 activators and oxidants provoked ATF3 induction in astrocytes, whereas its expression was reduced in Nrf2-depleted cells. We further demonstrated that the consensus ARE in the ATF3 promoter is critical for Nrf2-mediation by promoter analyses using an ATF3 promoter-driven luciferase construct and a chromatin immunoprecipitation assay. In addition, we found that Nrf2-dependent ATF3 induction contributed to the antioxidative and cytoprotective functions of Nrf2 in astrocytes. Taken together, our findings suggest that ATF3 is a new target for Nrf2 and has a cytoprotective function in astrocytes.
ISSN
0305-1048
URI
https://hdl.handle.net/10371/172648
DOI
https://doi.org/10.1093/nar/gkp865
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Graduate School of Convergence Science and Technology (융합과학기술대학원)Dept. of Molecular and Biopharmaceutical Sciences (분자의학 및 바이오제약학과)Journal Papers (저널논문_분자의학 및 바이오제약학과)
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