Journal
BIOCHEMICAL JOURNAL
Volume 457, Issue -, Pages 415-424Publisher
PORTLAND PRESS LTD
DOI: 10.1042/BJ20130863
Keywords
ATP; FAD; fatty acid oxidation; Kelch-like ECH-associated protein 1 (Keap1); live-cell imaging; tissue slice
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Funding
- Cancer Research UK [C20953/A10270]
- Wellcome Trust/MRC Parkinson's Consortium Grant
- MRC [MC_G1000735] Funding Source: UKRI
- Cancer Research UK [10270] Funding Source: researchfish
- Medical Research Council [MC_G1000735] Funding Source: researchfish
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Transcription factor Nrf2 (NF-E2 p45-related factor 2) regulates the cellular redox homoeostasis and cytoprotective responses, allowing adaptation and survival under conditions of stress. The significance of Nrf2 in intermediary metabolism is also beginning to be recognized. Thus this transcription factor negatively affects fatty acid synthesis. However, the effect of Nrf2 on fatty acid oxidation is currently unknown. In the present paper, we report that the mitochondrial oxidation of long-chain (palmitic) and short-chain (hexanoic) fatty acids is depressed in the absence of Nrf2 and accelerated when Nrf2 is constitutively active. Addition of fatty acids stimulates respiration in heart and liver mitochondria isolated from wild-type mice. This effect is significantly weaker when Nrf2 is deleted, whereas it is stronger when Nrf2 activity is constitutively high. In the absence of glucose, addition of fatty acids differentially affects the production of ATP in mouse embryonic fibroblasts from wild-type, Nrf2-knockout and Keap1 (Kelch-like ECH-associated protein 1)-knockout mice. In acute tissue slices, the rate of regeneration of FADH(2) is reduced when Nrf2 is absent. This metabolic role of Nrf2 on fatty acid oxidation has implications for chronic disease conditions including cancer, metabolic syndrome and neurodegeneration.
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