Cardiolipin content controls mitochondrial coupling and energetic efficiency in muscle

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Prola, Alexandre | Blondelle, Jordan | Vandestienne, Aymeline | Piquereau, Jérôme | Denis, Raphaël | Guyot, Stéphane | Chauvin, Hadrien | Mourier, Arnaud | Maurer, Marie | Henry, Céline | Khadhraoui, Nahed | Gallerne, Cindy | Molinié, Thibaut | Courtin, Guillaume | Guillaud, Laurent | Gressette, Mélanie | Solgadi, Audrey | Dumont, Florent | Castel, Julien | Ternacle, Julien | Demarquoy, Jean | Malgoyre, Alexandra | Koulmann, Nathalie | Derumeaux, Geneviève | Giraud, Marie-france | Joubert, Frederic | Veksler, Vladimir | Luquet, Serge | Relaix, Frédéric | Tiret, Laurent | Pilot-Storck, Fanny

Edité par CCSD ; American Association for the Advancement of Science (AAAS) -

International audience. Unbalanced energy partitioning participates in the rise of obesity, a major public health concern in many countries. Increasing basal energy expenditure has been proposed as a strategy to fight obesity yet raises efficiency and safety concerns. Here, we show that mice deficient for a muscle-specific enzyme of very-long-chain fatty acid synthesis display increased basal energy expenditure and protection against high-fat diet–induced obesity. Mechanistically, muscle-specific modulation of the very-long-chain fatty acid pathway was associated with a reduced content of the inner mitochondrial membrane phospholipid cardiolipin and a blunted coupling efficiency between the respiratory chain and adenosine 5′-triphosphate (ATP) synthase, which was restored by cardiolipin enrichment. Our study reveals that selective increase of lipid oxidative capacities in skeletal muscle, through the cardiolipin-dependent lowering of mitochondrial ATP production, provides an effective option against obesity at the whole-body level.

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