Department of Psychology and Neuroscience, Trinity College of Arts and Sciences, Duke University, Durham, NC 27710, USA.
Department of Cell Biology, Duke University Medical Center, Durham, NC 27710, USA.
Cell Rep. 2022 Aug 2;40(5):111161. doi: 10.1016/j.celrep.2022.111161.
Gestational exposure to environmental toxins and socioeconomic stressors is epidemiologically linked to neurodevelopmental disorders with strong male bias, such as autism. We model these prenatal risk factors in mice by co-exposing pregnant dams to an environmental pollutant and limited-resource stress, which robustly activates the maternal immune system. Only male offspring display long-lasting behavioral abnormalities and alterations in the activity of brain networks encoding social interactions. Cellularly, prenatal stressors diminish microglial function within the anterior cingulate cortex, a central node of the social coding network, in males during early postnatal development. Precise inhibition of microglial phagocytosis within the anterior cingulate cortex (ACC) of wild-type (WT) mice during the same critical period mimics the impact of prenatal stressors on a male-specific behavior, indicating that environmental stressors alter neural circuit formation in males via impairing microglia function during development.
妊娠期间暴露于环境毒素和社会经济压力源与神经发育障碍有关,这些障碍具有强烈的男性偏向,如自闭症。我们通过同时使怀孕的母鼠暴露于环境污染物和资源有限的应激中来在小鼠中模拟这些产前风险因素,这会强烈激活母体免疫系统。只有雄性后代表现出持久的行为异常和社交互动编码脑网络活动的改变。从细胞水平上讲,在雄性幼仔的早期发育过程中,产前应激源会降低扣带前皮质(ACC)中的小胶质细胞功能,而扣带前皮质是社交编码网络的中央节点。在同一关键时期,对野生型(WT)小鼠扣带前皮质(ACC)中的小胶质细胞吞噬作用进行精确抑制,可模拟产前应激源对雄性特异性行为的影响,表明环境应激源通过在发育过程中损害小胶质细胞功能来改变雄性的神经回路形成。