Prostaglandin PGE2 Receptor EP4 Regulates Microglial Phagocytosis and Increases Susceptibility to Diet-Induced Obesity

• Published in: Diabetes (New York, N.Y.) Vol. 72; no. 2; pp. 233 - 244
• Main Authors: Niraula, Anzela, Fasnacht, Rachael D, Ness, Kelly M, Frey, Jeremy M, Cuschieri, Sophia A, Dorfman, Mauricio D, Thaler, Joshua P
• Format: Journal Article
• Language: English
• Published: United States American Diabetes Association 01.02.2023
• Subjects: Animals; Axons; Body weight gain; Brain architecture; Diet, High-Fat - adverse effects; Dinoprostone - metabolism; Energy balance; Food intake; Glucose tolerance; High fat diet; Hypothalamus; Insulin; Insulin resistance; Mice; Mice, Inbred C57BL; Mice, Knockout; Microglia; Microglia - metabolism; Obesity; Obesity - genetics; Obesity - metabolism; Obesity Studies; Paraventricular nucleus; Phagocytes; Phagocytosis; Phenotypes; Pro-Opiomelanocortin - metabolism; Proopiomelanocortin; Prostaglandin E2; Weight Gain
• ISSN: 0012-1797; 1939-327X; 1939-327X
• DOI: 10.2337/db21-1072

In rodents, susceptibility to diet-induced obesity requires microglial activation, but the molecular components of this pathway remain incompletely defined. Prostaglandin PGE2 levels increase in the mediobasal hypothalamus during high-fat-diet (HFD) feeding, and the PGE2 receptor EP4 regulates microglial activation state and phagocytic activity, suggesting a potential role for microglial EP4 signaling in obesity pathogenesis. To test the role of microglial EP4 in energy balance regulation, we analyzed the metabolic phenotype in a microglia-specific EP4 knockout (MG-EP4 KO) mouse model. Microglial EP4 deletion markedly reduced weight gain and food intake in response to HFD feeding. Corresponding with this lean phenotype, insulin sensitivity was also improved in HFD-fed MG-EP4 KO mice, though glucose tolerance remained surprisingly unaffected. Mechanistically, EP4-deficient microglia showed an attenuated phagocytic state marked by reduced CD68 expression and fewer contacts with pro-opiomelanocortin (POMC) neuron processes. These cellular changes observed in the MG-EP4 KO mice corresponded with an increased density of POMC neurites extending into the paraventricular nucleus (PVN). These findings reveal that microglial EP4 signaling promotes body weight gain and insulin resistance during HFD feeding. Furthermore, the data suggest that curbing microglial phagocytic function may preserve POMC cytoarchitecture and PVN input to limit overconsumption during diet-induced obesity.