An acute microglial metabolic response controls metabolism and improves memory

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

doi:10.7554/eLife.87120.3

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学術論文

An acute microglial metabolic response controls metabolism and improves memory

MPS-Authors

Drougard, Anne
Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

Wegert, Vanessa
Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

Panzeri, Ilaria
Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

Schaf, Judith
Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

Gossens, Klaus
Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

Völker, Josephine
Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

Bremser, Anna
Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

Dror, Erez
Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

Sagar, Sagar
Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

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Pospisilik, John Andrew
Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society;

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https://elifesciences.org/articles/87120
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10.7554_eLife.87120.pdf
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引用

Drougard, A., Ma, E. H., Wegert, V., Sheldon, R., Panzeri, I., Vatsa, N., Apostle, S., Fagnocchi, L., Schaf, J., Gossens, K., Völker, J., Pang, S., Bremser, A., Dror, E., Giacona, F., Sagar, S., Henderson, M. X., Prinz, M., Jones, R. G., & Pospisilik, J. A. (2024). An acute microglial metabolic response controls metabolism and improves memory. eLife, 12:. doi:10.7554/eLife.87120.3.

引用: https://hdl.handle.net/21.11116/0000-0010-EAAD-4

要旨

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.