TY - JOUR T1 - Blocking mitochondrial pyruvate import causes energy wasting via futile lipid cycling in brown fat JF - bioRxiv DO - 10.1101/841551 SP - 841551 AU - Michaela Veliova AU - Caroline M. Ferreira AU - Ilan Y. Benador AU - Anthony E. Jones AU - Brandon R. Desousa AU - Kiana Mahdaviani AU - Rebeca Acín-Pérez AU - Anton Petcherski AU - Ajit S. Divakaruni AU - Marc Prentki AU - Barbara E. Corkey AU - Marc Liesa AU - Marcus F. Oliveira AU - Orian S. Shirihai Y1 - 2019/01/01 UR - http://biorxiv.org/content/early/2019/11/15/841551.abstract N2 - Futile lipid cycling is an ATP-wasting process proposed to participate in energy expenditure of mature fat-storing white adipocytes, given their inability to oxidize fat. The hallmark of activated brown adipocytes is to increase fat oxidation by uncoupling respiration from ATP synthesis. Whether ATP-consuming lipid cycling can contribute to BAT energy expenditure has been largely unexplored. Here we find that pharmacological inhibition of the mitochondrial pyruvate carrier (MPC) in brown adipocytes is sufficient to increase ATP-synthesis fueled by fatty acid oxidation, even in the absence of adrenergic stimulation. We find that elevated ATP-demand induced by MPC inhibition results from activation of futile lipid cycling. Furthermore, we identify that glutamine consumption and the Malate-Aspartate Shuttle are required for the increase in Energy Expenditure induced by MPC inhibition in Brown Adipocytes (MAShEEBA). These data demonstrate that futile energy expenditure through lipid cycling can be activated in BAT by altering fuel availability to mitochondria. Therefore, we identify a new mechanism to increase fat oxidation and energy expenditure in BAT that bypasses the need for adrenergic stimulation of mitochondrial uncoupling. ER -