期刊
FREE RADICAL BIOLOGY AND MEDICINE
卷 46, 期 4, 页码 443-453出版社
ELSEVIER SCIENCE INC
DOI: 10.1016/j.freeradbiomed.2008.10.040
关键词
Nrf2; Oxidative stress; Glutathione; Glutathione reductase; Cigarette smoke; COPD; Emphysema; Free radicals
资金
- NIH [HL081205]
- NHLBI SCCOR [P50HL084945]
- FAMRI, a Maryland Cigarette Restitution Fund [GM079239]
- NIEHS Center [ES03819]
- NIEHS [ES07141]
Nuclear factor-erythroid 2 p45-related factor 2 (NrF2) is the primary transcription factor protecting cells from oxidative Stress by regulating cytoprotective genes, including the antioxidant glutathione (GSH) pathway. GSH maintains cellular redox status and affects redox signaling, cell proliferation, and death. GSH homeostasis is regulated by de novo synthesis as well as GSH redox state; previous studies have demonstrated that Nrf2 regulates GSH homeostasis by affecting de novo synthesis. We report that Nrf2 modulates the GSH redox state by regulating glutathione reductase (GSR). In response to oxidants, lungs and embryonic fibroblasts (MEFs) front Nrf2-deficient (Ntf2(-/-)) mice showed lower levels of GSR mRNA, protein, and enzyme activity relative to wild type (Nrf2(+/+)). Nrf2(-/-) MEFs exhibited greater accumulation of glutathione disulfide and cytotoxicity compared to Nrf(+/+) MEFs in response to t-butylydroquinone, which was rescued by restoring GSR. Microinjection of glutathione disulfide induced greater apoptosis in Nrf2(-/-) MEFs compared to Nrf2(+/+) MEFs. In silico promoter analysis of the GSR gene revealed three Putative antioxidant-response elements (ARE1, -44; ARE2, -813; ARE3, -1041). Reporter analysis, site-directed mutagenesis, and chromatin immunoprecipitation assays demonstrated binding of Nrf2 to two AREs distal to the transcription start site. Overall, Nrf2 is Critical for maintaining the GSH redox state via transcriptional regulation of GSR and protecting cells against oxidative Stress. (C) 2008 Elsevier Inc. All rights reserved.
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