Department of Psychiatry, Washington University School of Medicine, St Louis, MO, 63110, USA.
Department of Genetics & Genome Technology Access Center, Washington University School of Medicine, St Louis, MO, 63110, USA.
J Neuroinflammation. 2024 Oct 5;21(1):251. doi: 10.1186/s12974-024-03233-1.
Neuroinflammation has been implicated in the pathogenesis of several neurologic and psychiatric disorders. Microglia are key drivers of neuroinflammation and, in response to different inflammatory stimuli, overexpress a proinflammatory signature of genes. Among these, Ch25h is a gene overexpressed in brain tissue from Alzheimer's disease as well as various mouse models of neuroinflammation. Ch25h encodes cholesterol 25-hydroxylase, an enzyme upregulated in activated microglia under conditions of neuroinflammation, that hydroxylates cholesterol to form 25-hydroxycholesterol (25HC). 25HC can be further metabolized to 7α,25-dihydroxycholesterol, which is a potent chemoattractant of leukocytes. We have previously shown that 25HC increases the production and secretion of the proinflammatory cytokine, IL-1β, by primary mouse microglia treated with lipopolysaccharide (LPS). In the present study, wildtype (WT) and Ch25h-knockout (KO) mice were peripherally administered LPS to induce an inflammatory state in the brain. In LPS-treated WT mice, Ch25h expression and 25HC levels increased in the brain relative to vehicle-treated WT mice. Among LPS-treated WT mice, females produced significantly higher levels of 25HC and showed transcriptomic changes reflecting higher levels of cytokine production and leukocyte migration than WT male mice. However, females were similar to males among LPS-treated KO mice. Ch25h-deficiency coincided with decreased microglial activation in response to systemic LPS. Proinflammatory cytokine production and intra-parenchymal infiltration of leukocytes were significantly lower in KO compared to WT mice. Amounts of IL-1β and IL-6 in the brain strongly correlated with 25HC levels. Our results suggest a proinflammatory role for 25HC in the brain following peripheral administration of LPS.
神经炎症与几种神经和精神疾病的发病机制有关。小胶质细胞是神经炎症的关键驱动因素,并且在响应不同的炎症刺激时,过度表达基因的促炎特征。在这些基因中,Ch25h 是在阿尔茨海默病的脑组织以及各种神经炎症的小鼠模型中过度表达的基因。Ch25h 编码胆固醇 25-羟化酶,该酶在神经炎症条件下被激活的小胶质细胞上调,将胆固醇羟基化为 25-羟胆固醇(25HC)。25HC 可以进一步代谢为 7α,25-二羟胆固醇,后者是白细胞的有效趋化因子。我们之前已经表明,25HC 增加了用脂多糖(LPS)处理的原代小鼠小胶质细胞中促炎细胞因子 IL-1β 的产生和分泌。在本研究中,野生型(WT)和 Ch25h 敲除(KO)小鼠经外周给予 LPS 以在大脑中诱导炎症状态。在 LPS 处理的 WT 小鼠中,Ch25h 的表达和 25HC 水平相对于 vehicle 处理的 WT 小鼠在脑中增加。在 LPS 处理的 WT 小鼠中,雌性产生的 25HC 水平明显高于 WT 雄性小鼠,并且反映细胞因子产生和白细胞迁移水平较高的转录组变化。然而,在 LPS 处理的 KO 小鼠中,雌性与雄性相似。Ch25h 缺陷与系统性 LPS 反应中小胶质细胞的激活减少有关。与 WT 小鼠相比,KO 小鼠中的促炎细胞因子产生和实质内白细胞浸润明显降低。大脑中的 IL-1β 和 IL-6 含量与 25HC 水平强烈相关。我们的结果表明,外周给予 LPS 后,25HC 在大脑中发挥促炎作用。