Phosphatidylethanolamine facilitates mitochondrial pyruvate entry to regulate metabolic flexibility

Siripoksup, P.; Cao, G.; Cluntun, A. A. A.; Maschek, J. A.; Pearce, Q.; Lang, M. J.; Eshima, H.; Opurum, P. C.; Mahmassani, Z. S.; Taylor, E. B.; Cox, J. E.; Drummond, M. J.; Rutter, J.; Funai, K.

doi:10.1101/2022.11.01.514767

bioRxiv · 10.1101/2022.11.01.514767

Phosphatidylethanolamine facilitates mitochondrial pyruvate entry to regulate metabolic flexibility

Siripoksup, P.·Cao, G.·Cluntun, A. A. A.·Maschek, J. A.·Pearce, Q.·Lang, M. J.·Eshima, H.·Opurum, P. C.·Mahmassani, Z. S.·Taylor, E. B.·Cox, J. E.·Drummond, M. J.·Rutter, J.·Funai, K.

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Abstract

Carbohydrates and lipids provide the majority of substrates to fuel mitochondrial oxidative phosphorylation (OXPHOS). Metabolic inflexibility, defined as an impaired ability to switch between these fuels, is implicated in a number of metabolic diseases. Here we explore the mechanism by which physical inactivity promotes metabolic inflexibility in skeletal muscle. We developed a mouse model of sedentariness by small mouse cage (SMC) that, unlike other classic models of disuse in mice, faithfully recapitulates metabolic responses that occur in humans. Bioenergetic phenotyping of mitochondria displayed metabolic inflexibility induced by physical inactivity, demonstrated by a reduction in pyruvate-stimulated respiration (JO2) in absence of a change in palmitate-stimulated JO2. Pyruvate resistance in these mitochondria was likely driven by a decrease in phosphatidylethanolamine (PE) abundance in the mitochondrial membrane. Reduction in mitochondrial PE by deletion of phosphatidylserine decarboxylase (PSD) was sufficient to induce metabolic inflexibility measured at the whole-body level, as well as at the level of skeletal muscle mitochondria. Low mitochondrial PE was sufficient to increase glucose flux towards lactate. We further implicate that resistance to pyruvate metabolism is due to attenuated mitochondrial entry via mitochondrial pyruvate carrier (MPC). These findings suggest a novel mechanism by which mitochondrial PE directly regulates MPC activity to modulate metabolic flexibility.

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Siripoksup, P., Cao, G., Cluntun, A. A. A., Maschek, J. A., Pearce, Q., Lang, M. J., Eshima, H., Opurum, P. C., Mahmassani, Z. S., Taylor, E. B., Cox, J. E., Drummond, M. J., Rutter, J., Funai, K.. 2022-11-02. Phosphatidylethanolamine facilitates mitochondrial pyruvate entry to regulate metabolic flexibility. https://doi.org/10.1101/2022.11.01.514767

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