Facial reconstruction

Search LJMU Research Online

Browse Repository | Browse E-Theses

Nrf2 impacts cellular bioenergetics by controlling substrate availability for mitochondrial respiration

Holmstrom, KM, Baird, L, Zhang, Y, Hargreaves, IP, Chalasani, A, Land, JM, Stanyer, L, Yamamoto, M, Dinkova-Kostova, AT and Abramov, AY (2013) Nrf2 impacts cellular bioenergetics by controlling substrate availability for mitochondrial respiration. Biology Open, 2 (8). pp. 761-770. ISSN 2046-6390

[img]
Preview
Text
Nrf2 impacts cellular bioenergetics by controlling substrate availability for mitochondrial respiration.pdf - Published Version
Available under License Creative Commons Attribution.

Download (1MB) | Preview

Abstract

Transcription factor Nrf2 and its repressor Keap1 regulate a network of cytoprotective genes involving more than 1% of the genome, their best known targets being drug-metabolizing and antioxidant genes. Here we demonstrate a novel role for this pathway in directly regulating mitochondrial bioenergetics in murine neurons and embryonic fibroblasts. Loss of Nrf2 leads to mitochondrial depolarisation, decreased ATP levels and impaired respiration, whereas genetic activation of Nrf2 increases the mitochondrial membrane potential and ATP levels, the rate of respiration and the efficiency of oxidative phosphorylation. We further show that Nrf2-deficient cells have increased production of ATP in glycolysis, which is then used by the F1Fo-ATPase for maintenance of the mitochondrial membrane potential. While the levels and in vitro activities of the respiratory complexes are unaffected by Nrf2 deletion, their activities in isolated mitochondria and intact live cells are substantially impaired. In addition, the rate of regeneration of NADH after inhibition of respiration is much slower in Nrf2-knockout cells than in their wild-type counterparts. Taken together, these results show that Nrf2 directly regulates cellular energy metabolism through modulating the availability of substrates for mitochondrial respiration. Our findings highlight the importance of efficient energy metabolism in Nrf2-mediated cytoprotection.

Item Type: Article
Uncontrolled Keywords: 0699 Other Biological Sciences
Subjects: Q Science > QH Natural history > QH301 Biology
Q Science > QH Natural history > QH426 Genetics
R Medicine > RM Therapeutics. Pharmacology
Divisions: Pharmacy & Biomolecular Sciences
Publisher: Company of Biologists
Related URLs:
Date Deposited: 22 Sep 2020 10:54
Last Modified: 22 Sep 2020 11:00
DOI or Identification number: 10.1242/bio.20134853
URI: https://researchonline.ljmu.ac.uk/id/eprint/13688

Actions (login required)

View Item View Item