INDUCTION OF THE KEAP1/NRF2/ARE PATHWAY BY OXIDIZABLE DIPHENOLS.
Summary of "INDUCTION OF THE KEAP1/NRF2/ARE PATHWAY BY OXIDIZABLE DIPHENOLS."
Inducible Keap1/Nrf2/ARE pathway determines the ability of multicellular organisms to adapt to conditions of stress caused by oxidants and electrophiles through upregulating proteins with versatile cytoprotective functions. Para- and ortho-hydroquinones were among the first identified small-molecule inducers of this pathway. Their oxidative lability strongly suggested that the electrophilic quinone metabolites, and not the hydroquinones themselves, were the ultimate inducers. Molecular orbital calculations re-enforced this notion by showing linear correlations between inducer potency and: (i) the ability of diphenols to release electrons, and (ii) the electron affinity of their corresponding quinones. Consequently, a two-step mechanism was proposed which involves oxidation of the diphenols to their corresponding quinone derivatives, followed by modification of specific cysteine residues of the sensor protein Keap1. Our finding that Cu(++), as well as other transition metals, enhanced induction by oxidizable diphenols provided a rationale to test this hypothesis. We found that hypoxia inhibits the potentiation of diphenolic inducer activity afforded by copper as oxygen is required to oxidize Cu(+) and regenerate Cu(++). In the stably transfected AREc32 reporter cell line, exposure to 2-tert-butyl-1,4-hydroquinone (tBHQ) for 30min induced ARE-luciferase (measured 24hours later) only in the presence of copper (Cu(++) or Cu(+)), whereas induction by tert-butyl-1,4-quinone (tBQ) was copper-independent. tBQ, but not tBHQ, reacts with cysteine residues of Keap1. Other para- and ortho- hydroquinones, such as catechol estrogens, dopamine, and L-DOPA, also induce ARE-driven transcription in a Cu(++)-dependent manner. Thus, based on theoretical and experimental evidence, the oxidation of para- and ortho- hydroquinones to their corresponding electrophilic quinones is a requisite step for the activation of the Keap1/Nrf2/ARE pathway.
Biomedical Research Institute, University of Dundee, Dundee DD1 9SY, Scotland, United Kingdom; Division of Clinical Pharmacology, Departments of Medicine and Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 2
This article was published in the following journal.
Name: Chemico-biological interactions
- PubMed Source: http://www.ncbi.nlm.nih.gov/pubmed/20846517
- DOI: http://dx.doi.org/10.1016/j.cbi.2010.09.010
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