PreprintCited by 68Mitochondrial Function and PathologyAdipose Tissue and MetabolismAutophagy in Disease and Therapy

Preserved respiratory chain capacity and physiology in mice with profoundly reduced levels of mitochondrial respirasomes

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Milenkovic, Dusanka, Misic, Jelena, Hevler, Johannes F, Molinié, Thibaut, Chung, Injae, Atanassov, Ilian, Li, Xinping, Filograna, Roberta +5 more·2023·Cell Metabolism

Preprint — published as 10.1016/j.cmet.2023.07.015 · Paper page

Abstract

SUMMARY: The mammalian respiratory chain complexes I, III 2 and IV (CI, CIII 2 and CIV) are critical for cellular bioenergetics and form a stable assembly, the respirasome (CI- CIII 2 -CIV), that is biochemically and structurally well documented. The role of the respirasome in bioenergetics and regulation of metabolism is subject to intense debate and is difficult to study because the individual respiratory chain complexes coexist together with high levels of respirasomes. To critically investigate the in vivo role of the respirasome, we generated homozygous knock-in mice that have normal levels of respiratory chain complexes but profoundly decreased levels of respirasomes. Surprisingly, the mutant mice are healthy, with preserved respiratory chain capacity and normal exercise performance. Our findings show that high levels of respirasomes are dispensable for maintaining bioenergetics and physiology in the mouse, but raises questions about their alternate functions, such as relating to regulation of protein stability and prevention of age-associated protein aggregation.

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Authors
Milenkovic, D., Misic, J., Hevler, J. F., Molinié, T., Chung, I., Atanassov, I., Li, X., Filograna, R., Mesaros, A., Mourier, A., Heck, A. J. R., Hirst, J., & Larsson, N.-G.
Affiliations
  • Max Planck Institute for Biology of Ageing (DE)
  • Karolinska Institutet (SE)
  • Utrecht University (NL)
  • Centre National de la Recherche Scientifique (FR)
  • University of Cambridge (GB)
Corresponding author
  • Hirst, Judy
  • Larsson, Nils-Göran
Venue
Cell Metabolism
Publisher
openRxiv
Published
2023-06-22
Volume
35
Issue
10
Pages
1799-1813.e7
ISSN
1550-4131 (ISSN-L)
OpenAlex
W4386171179
Cited by
68
References
1
Citations by year
2026: 14 · 2025: 25 · 2024: 23 · 2023: 6
FWCI
6.01
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Cell Metabolism (publishedVersion, cc-by)
  • bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion)
  • PubMed (publishedVersion)
  • HAL (submittedVersion, cc-by)
  • Apollo (University of Cambridge) (submittedVersion, cc-by)
  • Utrecht University Repository (Utrecht University) (submittedVersion, other-oa)
Funders
  • Swedish Cancer Foundation
  • Nederlandse Organisatie voor Wetenschappelijk Onderzoek (SPI.2017.028, 184.034.019)
  • Knut och Alice Wallenbergs Stiftelse (2019.0109, 2016.0050)
  • Max-Planck-Gesellschaft
  • Novo Nordisk
  • Vetenskapsrådet (2015-00418)
  • Novo Nordisk Fonden (NNF22OC0078444, NNF20OC0063616, NNF20OC006316)
  • Medical Research Council (MC_UU_00015/2, MC_U105663141, MC_UU_00015/7)
  • H2020 European Research Council (741366)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
  • Health Sciences › Medicine › Physiology › Adipose Tissue and Metabolism
  • Health Sciences › Medicine › Epidemiology › Autophagy in Disease and Therapy
Keywords
respirasome, electron transport chain, cytochrome c oxidase, mitochondrial bioenergetics, knock-in mice, exercise performance, protein stability, protein aggregation
MeSH terms
Animals, Electron Transport Complex IV, Electron Transport, Energy Metabolism, Mammals, Mitochondria, Mitochondrial Membranes, Mice

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