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An acute microglial metabolic response controls metabolism and improves memory.

Anne Drougard | Eric H Ma | Vanessa Wegert | Ryan Sheldon | Ilaria Panzeri | Naman Vatsa | Stefanos Apostle | Luca Fagnocchi | Judith Schaf | Klaus Gossens | Josephine Völker | Shengru Pang | Anna Bremser | Erez Dror | Francesca Giacona | Sagar Sagar | Michael X Henderson | Marco Prinz | Russell G Jones | John Andrew Pospisilik
eLife | 2024

Chronic high-fat feeding triggers metabolic dysfunction including obesity, insulin resistance, and diabetes. How high-fat intake first triggers these pathophysiological states remains unknown. Here, we identify an acute microglial metabolic response that rapidly translates intake of high-fat diet (HFD) to a surprisingly beneficial effect on metabolism and spatial/learning memory. High-fat intake rapidly increases palmitate levels in cerebrospinal fluid and triggers a wave of microglial metabolic activation characterized by mitochondrial membrane activation and fission as well as metabolic skewing toward aerobic glycolysis. These effects are detectable throughout the brain and can be detected within as little as 12 hr of HFD exposure. In vivo, microglial ablation and conditional DRP1 deletion show that the microglial metabolic response is necessary for the acute effects of HFD. 13C-tracing experiments reveal that in addition to processing via β-oxidation, microglia shunt a substantial fraction of palmitate toward anaplerosis and re-release of bioenergetic carbons into the extracellular milieu in the form of lactate, glutamate, succinate, and intriguingly, the neuroprotective metabolite itaconate. Together, these data identify microglia as a critical nutrient regulatory node in the brain, metabolizing away harmful fatty acids and liberating the same carbons as alternate bioenergetic and protective substrates for surrounding cells. The data identify a surprisingly beneficial effect of short-term HFD on learning and memory.

Pubmed ID: 39625057

Associated grants

  • Agency: NHGRI NIH HHS, United States
    Id: R21 HG011964
  • Agency: Deutsche Forschungsgemeinschaft,
    Id: NeuroMac - CRC/TRR167
  • Agency: NIH HHS, United States
    Id: R21HG011964
  • Agency: Marie Sklodowska-Curie Actions,
    Id: 10.3030/707123
  • Agency: NHGRI NIH HHS, United States
    Id: R01 HG012444
  • Agency: Marie Sklodowska-Curie Actions,
    Id: 10.3030/675610
  • Agency: NIH HHS, United States
    Id: 1R01HG012444

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