Gironda Stephen C, Centanni Samuel W, Weiner Jeffrey L
bioRxiv. 2024 Aug 12:2024.07.27.605403. doi: 10.1101/2024.07.27.605403.
Early life stress (ELS) has lasting consequences on microglia and brain macrophage function. During ELS, microglia and brain macrophages alter their engagement with synapses leading to changes in neuronal excitability. Further, ELS can induce innate immune memory formation in microglia and brain macrophages resulting in altered responsivity to future environmental stimuli. These alterations can result in lasting adaptations in circuit function and may mediate the relationship between ELS and the risk to develop alcohol use disorder (AUD). Whether microglia and brain macrophages truly mediate this relationship remains elusive. Here, we report: 1) an ELS model, psychosocial stress (PSS), increases binge-like ethanol consumption in early adulthood. 2) Repeated binge-like ethanol consumption increases microglia and brain macrophage population densities across the brain. 3) PSS may elicit innate immune memory formation in microglia and brain macrophages leading to altered population densities following repeated binge-like ethanol consumption. 4) Microglia and brain macrophage inhibition trended towards preventing PSS-evoked changes in binge-like ethanol consumption and normalized microglia and brain macrophage population densities. Therefore, our study suggests that acutely inhibiting microglia and brain macrophage function during periods of early life PSS may prevent innate immune memory formation and assist in reducing the risk to develop AUD.
An early life psychosocial stress (PSS) exposure increases ethanol consumptionMicroglial inhibition during PSS trends towards reducing ethanol consumptionBinge ethanol consumption increases microglial count and alters cell proximityEarly life PSS alters microglial responsivity to binge ethanol consumptionMicroglial inhibition may prevent microglial innate immune memory formation.
早年生活应激(ELS)对小胶质细胞和脑巨噬细胞功能有持久影响。在ELS期间,小胶质细胞和脑巨噬细胞改变它们与突触的相互作用,导致神经元兴奋性发生变化。此外,ELS可诱导小胶质细胞和脑巨噬细胞形成先天性免疫记忆,从而改变对未来环境刺激的反应性。这些改变可导致神经回路功能的持久适应性变化,并可能介导ELS与发生酒精使用障碍(AUD)风险之间的关系。小胶质细胞和脑巨噬细胞是否真的介导这种关系仍不清楚。在此,我们报告:1)一种ELS模型,即心理社会应激(PSS),会增加成年早期类似暴饮的乙醇摄入量。2)反复进行类似暴饮的乙醇摄入会增加全脑小胶质细胞和脑巨噬细胞的群体密度。3)PSS可能引发小胶质细胞和脑巨噬细胞中的先天性免疫记忆形成,导致在反复进行类似暴饮的乙醇摄入后群体密度发生改变。4)抑制小胶质细胞和脑巨噬细胞有阻止PSS引起的类似暴饮的乙醇摄入量变化的趋势,并使小胶质细胞和脑巨噬细胞群体密度恢复正常。因此,我们的研究表明,在早年生活PSS期间急性抑制小胶质细胞和脑巨噬细胞功能可能会阻止先天性免疫记忆形成,并有助于降低发生AUD的风险。
早年心理社会应激(PSS)暴露会增加乙醇摄入量;PSS期间抑制小胶质细胞有减少乙醇摄入量的趋势;暴饮乙醇会增加小胶质细胞数量并改变细胞间距;早年PSS会改变小胶质细胞对暴饮乙醇的反应性;抑制小胶质细胞可能会阻止小胶质细胞先天性免疫记忆形成。