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Key role of MIF-related neuroinflammation in neurodegeneration and cognitive impairment in Alzheimer’s disease

机译:MIF相关的神经炎症在阿尔茨海默病的神经变性和认知障碍中的关键作用

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摘要

In-vitro results of STZ stimulation on murine Microglia and Astrocytes. ELISA of MIF secretion in supernatants of astrocytes and microglia after 24 h STZ treatment. Graphs represent the mean of  = 3 biological replicates (two technical replicates for each) with standard errors of the mean (± SEM), (*  b and mRNA expression levels for different cytokine in response to STZ treatment in astrocytes ( ) and microglia ( ) with and without ISO-1 treatment. - . Cytokine ELISA of astrocytes after 24 h STZ treatment. Data are means of  = 3 independent biological replicates, error bars represents ± SEM (*  d), IL-1β ( ) and IL-12p40 ( ) were released in response to STZ treatment in astrocytes using different concentrations of ISO-1 to inhibit MIF resulted in dose dependent decrease in cytokine release in both cell types. Cytokine ELISA in wild type microglia. IL-6 ( ) IL-1β ( ) and IL-10 ( ) were measured after STZ treatment with and without ISO-1. One-way ANOVA with Tukey’s multiple comparison test was performed. (*  P
机译:STZ刺激小鼠小胶质细胞和星形胶质细胞的体外结果。 STZ处理24小时后,星形胶质细胞和小胶质细胞上清液中MIF分泌的ELISA。图形代表= 3生物学重复的平均值(每个重复两次,每个均重复两次),标准差的平均值为(±SEM),(* b和星形胶质细胞和小胶质细胞对STZ处理后不同细胞因子的mRNA表达水平)进行和不进行ISO-1处理的情况-。STZ处理24小时后星形胶质细胞的细胞因子ELISA。数据是= 3个独立的生物学重复的平均值,误差线代表±SEM(* d),IL-1β()和IL-12p40(分别在星形胶质细胞中使用不同浓度的ISO-1抑制MIF释放星形胶质瘤以响应STZ处理,导致两种细胞类型中细胞因子的释放呈剂量依赖性降低;野生型小胶质细胞因子ELISA; IL-6()IL-1β()在有或没有ISO-1的STZ处理后,测定IL-10()和IL-10()。采用Tukey的多重比较测试进行单向ANOVA(* P

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