Food perception promotes phosphorylation of MFFS131 and mitochondrial fragmentation in liver

Author:

Henschke Sinika123ORCID,Nolte Hendrik34ORCID,Magoley Judith123ORCID,Kleele Tatjana5,Brandt Claus123ORCID,Hausen A. Christine123ORCID,Wunderlich Claudia M.123ORCID,Bauder Corinna A.123ORCID,Aschauer Philipp6ORCID,Manley Suliana5ORCID,Langer Thomas34ORCID,Wunderlich F. Thomas123ORCID,Brüning Jens C.1237ORCID

Affiliation:

1. Max Planck Institute for Metabolism Research, Department of Neuronal Control of Metabolism, Cologne, Germany.

2. Policlinic for Endocrinology, Diabetes and Preventive Medicine (PEDP), University Hospital Cologne, Cologne, Germany.

3. Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases (CECAD) and Center of Molecular Medicine Cologne (CMMC), University of Cologne, Cologne, Germany.

4. Max Planck Institute for Biology of Ageing, Cologne, Germany.

5. Institute of Physics, École Polytechnique Fédérale de Lausanne (EPFL), Lausanne, Switzerland.

6. Institute of Molecular Biosciences, University of Graz, Graz, Austria.

7. National Center for Diabetes Research (DZD), Neuherberg, Germany.

Abstract

Liver mitochondria play a central role in metabolic adaptations to changing nutritional states, yet their dynamic regulation upon anticipated changes in nutrient availability has remained unaddressed. Here, we found that sensory food perception rapidly induced mitochondrial fragmentation in the liver through protein kinase B/AKT (AKT)–dependent phosphorylation of serine 131 of the mitochondrial fission factor (MFFS131). This response was mediated by activation of hypothalamic pro-opiomelanocortin (POMC)–expressing neurons. A nonphosphorylatable MFF S131G knock-in mutation abrogated AKT-induced mitochondrial fragmentation in vitro. In vivo, MFF S131G knock-in mice displayed altered liver mitochondrial dynamics and impaired insulin-stimulated suppression of hepatic glucose production. Thus, rapid activation of a hypothalamus–liver axis can adapt mitochondrial function to anticipated changes of nutritional state in control of hepatic glucose metabolism.

Publisher

American Association for the Advancement of Science (AAAS)

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