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Maternal high-fat diet drives sex-specific microglia remodeling of serotonergic reward circuitry

Michael S. PattoniD, William Sun, Lillian Stanley, Aasha Paredes, Joanna Kang, Zachary Schettewi, Benjamin L. HorvathiD, Julia E. DziabisiD, Benjamin A. DevliniD, Trisha V. VaidyanathaniD, Staci D. BilboiD

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Abstract

Maternal nutrition shapes offspring brain development and influences neurodevelopmental disorder risk, but the underlying mechanisms remain unclear. In mice, maternal high-fat diet exposure disrupted microglia-serotonin interactions during a critical postnatal period, producing persistent, sex-specific mesolimbic alterations. Male but not female offspring showed increased serotonergic fiber density in the nucleus accumbens (NAc), coincident with reduced microglial phagocytosis of serotonergic projections. Microglial 5-HT2C receptor signaling is a key regulator of this process. Viral over expression in microglia, mimicking diet-induced upregulation, was sufficient to cause serotonergic hyperinnervation. By adulthood, male offspring displayed increased NAc serotonin release and projection-specific changes in dorsal raphe physiology. These circuit alterations accelerated reward-motivated learning, a phenotype reproduced by chemogenetic activation of NAc-projecting serotonergic neurons. Together, these findings reveal a novel mechanism by which maternal diet programs serotonergic circuit assembly and behavior in a sex-specific manner, providing a potential link between early-life metabolic inflammation and lifelong serotonergic dysfunction.

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