首页|PACS-2在阿尔茨海默病发展中作用机制研究

PACS-2在阿尔茨海默病发展中作用机制研究

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目的 探究磷酸呋喃酸性簇分选蛋白-2(phosphofurin acidic cluster sorting protein-2,PACS-2)在N2a/APP695swe细胞线粒体功能及细胞凋亡中的参与作用,进一步探讨PACS-2 在阿尔茨海默病(Alzheimer's disease,AD)发生、发展中的作用及意义.方法 CCK8 法分析不同浓度的二苯乙烯苷(tetrahydroxy stilbene glycoside,TSG)处理N2a/APP695swe细胞 48h后的细胞存活率,选择合适浓度的TSG用于后续实验.体外常规培养N2a/WT细胞和N2a/APP695swe细胞,实验细胞分为 3 个组:空白对照组(WT组):N2a/WT细胞;模型组(APP组):N2a/APP695swe细胞;治疗组(TSG组):N2a/APP695swe细胞,合适浓度的TSG干预.TUNEL法荧光显微镜观察细胞凋亡情况,JC-1 法流式检测细胞线粒体膜电位,Western blot(WB)检测PACS-2 的蛋白表达情况,RT-qPCR检测PACS-2 的mRNA表达情况.结果 CCK8法分析不同浓度的TSG作用细胞48h后的细胞存活率:100μmol/L的TSG保护作用最显著,差异有统计学意义(P<0.01);TUNEL法荧光显微镜观察细胞凋亡情况,与WT组相比,APP组的凋亡率升高,与APP组相比,TSG组的凋亡率降低,差异有统计学意义(P<0.05);JC-1 法检测细胞线粒体膜电位;与WT组相比,APP组的膜电位降低,与APP组相比,TSG组膜电位升高,差异有统计学意义(P<0.05);WB检测PACS-2 的蛋白表达:与WT组相比,APP组的PACS-2 表达升高,与APP组相比,TSG组的PACS-2 表达降低,差异有统计学意义(P<0.05);RT-qPCR检测PACS-2 的mRNA表达:与WT组相比,APP组的PACS-2表达升高,与APP组相比,TSG组的PACS-2表达降低,差异有统计学意义(P<0.05).结论 PACS-2 在AD的发生、发展中有重要作用,其上调可能促进AD的发生,脑保护药物TSG可能通过下调PACS-2抑制AD模型细胞凋亡并改善线粒体功能发挥细胞保护作用.
Effect of PACS-2 on the development of Alzheimer's disease
Objective To investigate the involvement of phosphofurin acidic cluster sorting protein-2(PACS-2)in mitochondrial function and apoptosis in N2a/APP695swe cells and further explore the role and significance of PACS-2 in the development of Alzheimer's disease(AD).Methods The CCK8 method was used to analyze the cell survival rate of N2a/APP695swe cells treated with different concentrations of tetrahydroxy stilbene glycoside(TSG)for 48h and to select the appropriate concentration of TSG for subsequent experiments.N2a/WT cells and N2a/APP695swe cells were routinely cultured in vitro,and the experimental cells were divided into 3 groups:blank control group(WT group):N2a/WT cells;model group(APP group):N2a/APP695swe cells;treatment group(TSG group):N2a/APP695swe cells with appropriate concentrations of TSG intervention.TUNEL method to observe apoptosis by fluorescence microscopy;JC-1 method for flow detection of cellular mitochondrial membrane potential;WB to detect protein expression of PACS-2;RT-qPCR to detect PACS-2 mRNA expression.Results CCK8 method was used to analyze the cell survival rate of different concentrations of TSG acting on cells after 48h:the protective effect of 100 μmol/L TSG was the most significant and the difference was statistically significant(P<0.01).The TUNEL method of fluorescence microscopy observed the apoptosis:compared with the WT group,the apoptosis rate of APP group was increased,compared with the APP group,the apoptosis rate of TSG group was decreased,and the differences were statistically significant(P<0.05).The JC-1 method was used to detect the mitochondrial membrane potential of cells:compared with the WT group,the membrane potential of APP group was decreased,compared with the APP group,the membrane potential of TSG group was increased,and the differences were statistically significant(P<0.05);Western blot(WB)detection of PACS-2 protein expression:compared with the WT group,PACS-2 expression was significantly higher in the APP group,and compared with the APP group,PACS-2 expression was significantly lower in the TSG group,with statistically significant differences(P<0.05);The RT-qPCR detected the mRNA expression of PACS-2:the expression of PACS-2 was elevated in the APP group compared with the WT group and decreased in the TSG group compared with the APP group,with statistically significant differences(P<0.05).Conclusion PACS-2 has an important role in the development of AD,and its upregulation may promote the development of AD.The cerebroprotective drug TSG may exert cytoprotective effects by downregulating PACS-2 to inhibit apoptosis and improve mitochondrial function in AD model cells.

Phosphofurin acidic cluster sorting protein-2Alzheimer's diseaseN2a/APP695swe cellMitochondrial dysfunctionApoptosis

王艳云、叶群英、钱军、刘志鹏、罗红波、李芸

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遵义医科大学第五附属(珠海)医院神经内科,广东珠海 519000

遵义医科大学第五附属(珠海)医院肾病风湿科,广东珠海 519000

PACS-2 阿尔茨海默病 N2a/APP695swe细胞 线粒体功能障碍 细胞凋亡

贵州省科技支撑计划项目遵义医科大学研究生科研立项基金项目广东省医学科学技术研究基金项目

黔科合支撑[2020]4Y128号ZYK51B2021047

2024

中国现代医生
中国医学科学院

中国现代医生

影响因子:1.571
ISSN:1673-9701
年,卷(期):2024.62(5)
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