Bordt Evan A, Moya Haley A, Jo Young Chan, Ravichandran Caitlin T, Bankowski Izabella M, Ceasrine Alexis M, McDougle Christopher J, Carlezon William A, Bilbo Staci D
Department of Pediatrics, Lurie Center for Autism, Massachusetts General Hospital for Children, Harvard Medical School, Boston, MA 02129, USA.
Department of Pediatrics, Lurie Center for Autism, Massachusetts General Hospital for Children, Harvard Medical School, Boston, MA 02129, USA; Department of Psychology and Neuroscience, Duke University, Durham, NC 27708, USA.
Brain Behav Immun. 2024 Jan;115:680-695. doi: 10.1016/j.bbi.2023.11.010. Epub 2023 Nov 14.
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.
在许多神经发育障碍(如自闭症谱系障碍)的患病率上存在强烈的男性偏向。然而,这种性别偏向背后的机制仍然难以捉摸。围产期感染与神经发育障碍发生风险增加有关。在这里,我们使用了一种早期生命免疫激活的小鼠模型,该模型仅在雄性小鼠中可靠地诱导社交行为缺陷。我们证明,社交行为中男性偏向的改变依赖于小胶质细胞免疫信号传导,并与线粒体形态、基因表达以及特别是小胶质细胞(大脑的固有免疫细胞)内的功能改变相关联。此外,我们表明,这种对早期生命免疫激活的行为和小胶质细胞线粒体易感性是由男性典型的围产期性腺激素激增所编程的。这些发现表明,雄性小鼠一生中的社交行为是由小胶质细胞特异性机制调节的,这些机制由早期发育中发生的事件所塑造。