Gonadal hormones impart male-biased behavioral vulnerabilities to immune activation via microglial mitochondrial function

性腺激素通过小胶质细胞线粒体功能赋予雄性个体对免疫激活的易感行为。

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作者:Evan A Bordt ,Haley A Moya ,Young Chan Jo ,Caitlin T Ravichandran ,Izabella M Bankowski ,Alexis M Ceasrine ,Christopher J McDougle ,William A Carlezon Jr ,Staci D Bilbo

Abstract

There is a strong male bias in the prevalence of many neurodevelopmental disorders such as autism spectrum disorder. However, the mechanisms underlying this sex bias remain elusive. Infection during the perinatal period is associated with an increased risk of neurodevelopmental disorder development. Here, we used a mouse model of early-life immune activation that reliably induces deficits in social behaviors only in males. We demonstrate that male-biased alterations in social behavior are dependent upon microglial immune signaling and are coupled to alterations in mitochondrial morphology, gene expression, and function specifically within microglia, the innate immune cells of the brain. Additionally, we show that this behavioral and microglial mitochondrial vulnerability to early-life immune activation is programmed by the male-typical perinatal gonadal hormone surge. These findings demonstrate that social behavior in males over the lifespan are regulated by microglia-specific mechanisms that are shaped by events that occur in early development.

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