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Acute RyR1 Ca2+ leak enhances NADH-linked mitochondrial respiratory capacity

Author

Listed:
  • Nadège Zanou

    (University of Lausanne)

  • Haikel Dridi

    (Columbia University Vagelos College of Physicians and Surgeons)

  • Steven Reiken

    (Columbia University Vagelos College of Physicians and Surgeons)

  • Tanes Imamura de Lima

    (École Polytechnique Fédérale de Lausanne (EPFL))

  • Chris Donnelly

    (University of Lausanne)

  • Umberto De Marchi

    (Nestlé Research – École Polytechnique Fédérale de Lausanne (EPFL))

  • Manuele Ferrini

    (University of Lausanne)

  • Jeremy Vidal

    (University of Lausanne)

  • Leah Sittenfeld

    (Columbia University Vagelos College of Physicians and Surgeons)

  • Jerome N. Feige

    (Nestlé Research – École Polytechnique Fédérale de Lausanne (EPFL)
    École Polytechnique Fédérale de Lausanne (EPFL))

  • Pablo M. Garcia-Roves

    (L’Hospitalet del Llobregat)

  • Isabel C. Lopez-Mejia

    (University of Lausanne)

  • Andrew R. Marks

    (Columbia University Vagelos College of Physicians and Surgeons
    Columbia University Medical Center)

  • Johan Auwerx

    (École Polytechnique Fédérale de Lausanne (EPFL))

  • Bengt Kayser

    (University of Lausanne)

  • Nicolas Place

    (University of Lausanne)

Abstract

Sustained ryanodine receptor (RyR) Ca2+ leak is associated with pathological conditions such as heart failure or skeletal muscle weakness. We report that a single session of sprint interval training (SIT), but not of moderate intensity continuous training (MICT), triggers RyR1 protein oxidation and nitrosylation leading to calstabin1 dissociation in healthy human muscle and in in vitro SIT models (simulated SIT or S-SIT). This is accompanied by decreased sarcoplasmic reticulum Ca2+ content, increased levels of mitochondrial oxidative phosphorylation proteins, supercomplex formation and enhanced NADH-linked mitochondrial respiratory capacity. Mechanistically, (S-)SIT increases mitochondrial Ca2+ uptake in mouse myotubes and muscle fibres, and decreases pyruvate dehydrogenase phosphorylation in human muscle and mouse myotubes. Countering Ca2+ leak or preventing mitochondrial Ca2+ uptake blunts S-SIT-induced adaptations, a result supported by proteomic analyses. Here we show that triggering acute transient Ca2+ leak through RyR1 in healthy muscle may contribute to the multiple health promoting benefits of exercise.

Suggested Citation

  • Nadège Zanou & Haikel Dridi & Steven Reiken & Tanes Imamura de Lima & Chris Donnelly & Umberto De Marchi & Manuele Ferrini & Jeremy Vidal & Leah Sittenfeld & Jerome N. Feige & Pablo M. Garcia-Roves & , 2021. "Acute RyR1 Ca2+ leak enhances NADH-linked mitochondrial respiratory capacity," Nature Communications, Nature, vol. 12(1), pages 1-19, December.
  • Handle: RePEc:nat:natcom:v:12:y:2021:i:1:d:10.1038_s41467-021-27422-1
    DOI: 10.1038/s41467-021-27422-1
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    References listed on IDEAS

    as
    1. Ran Zalk & Oliver B. Clarke & Amédée des Georges & Robert A. Grassucci & Steven Reiken & Filippo Mancia & Wayne A. Hendrickson & Joachim Frank & Andrew R. Marks, 2015. "Structure of a mammalian ryanodine receptor," Nature, Nature, vol. 517(7532), pages 44-49, January.
    2. Carles Cantó & Zachary Gerhart-Hines & Jerome N. Feige & Marie Lagouge & Lilia Noriega & Jill C. Milne & Peter J. Elliott & Pere Puigserver & Johan Auwerx, 2009. "AMPK regulates energy expenditure by modulating NAD+ metabolism and SIRT1 activity," Nature, Nature, vol. 458(7241), pages 1056-1060, April.
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