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Overexpression of mitochondrial sirtuins alters glycolysis and mitochondrial function in HEK293 cells

De Moura, MB and Uppala, R and Zhang, Y and Van Houten, B and Goetzman, ES (2014) Overexpression of mitochondrial sirtuins alters glycolysis and mitochondrial function in HEK293 cells. PLoS ONE, 9 (8).

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Abstract

SIRT3, SIRT4, and SIRT5 are mitochondrial deacylases that impact multiple facets of energy metabolism and mitochondrial function. SIRT3 activates several mitochondrial enzymes, SIRT4 represses its targets, and SIRT5 has been shown to both activate and repress mitochondrial enzymes. To gain insight into the relative effects of the mitochondrial sirtuins in governing mitochondrial energy metabolism, SIRT3, SIRT4, and SIRT5 overexpressing HEK293 cells were directly compared. When grown under standard cell culture conditions (25 mM glucose) all three sirtuins induced increases in mitochondrial respiration, glycolysis, and glucose oxidation, but with no change in growth rate or in steady-state ATP concentration. Increased proton leak, as evidenced by oxygen consumption in the presence of oligomycin, appeared to explain much of the increase in basal oxygen utilization. Growth in 5 mM glucose normalized the elevations in basal oxygen consumption, proton leak, and glycolysis in all sirtuin over-expressing cells. While the above effects were common to all three mitochondrial sirtuins, some differences between the SIRT3, SIRT4, and SIRT5 expressing cells were noted. Only SIRT3 overexpression affected fatty acid metabolism, and only SIRT4 overexpression altered superoxide levels and mitochondrial membrane potential. We conclude that all three mitochondrial sirtuins can promote increased mitochondrial respiration and cellular metabolism. SIRT3, SIRT4, and SIRT5 appear to respond to excess glucose by inducing a coordinated increase of glycolysis and respiration, with the excess energy dissipated via proton leak. © 2014 Barbi de Moura et al.


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Details

Item Type: Article
Status: Published
Creators/Authors:
CreatorsEmailPitt UsernameORCID
De Moura, MB
Uppala, Rrru4@pitt.eduRRU4
Zhang, Yyuz29@pitt.eduYUZ29
Van Houten, Bbev15@pitt.eduBEV15
Goetzman, ESesg5@pitt.eduESG5
Contributors:
ContributionContributors NameEmailPitt UsernameORCID
EditorLluch, Guillermo LópezUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Centers: Other Centers, Institutes, Offices, or Units > Pittsburgh Cancer Institute
Date: 28 August 2014
Date Type: Publication
Journal or Publication Title: PLoS ONE
Volume: 9
Number: 8
DOI or Unique Handle: 10.1371/journal.pone.0106028
Schools and Programs: School of Medicine > Pediatrics
School of Medicine > Pharmacology and Chemical Biology
Refereed: Yes
Date Deposited: 23 Sep 2014 15:09
Last Modified: 04 Feb 2019 18:55
URI: http://d-scholarship.pitt.edu/id/eprint/22989

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