转染
葛兰素史克-3
脂质体
糖原合酶
分子生物学
磷酸化
基因敲除
载脂蛋白E
τ蛋白
小干扰RNA
GSK3B公司
化学
质粒
污渍
生物
细胞生物学
重组DNA
内科学
基因
医学
生物化学
阿尔茨海默病
载体(分子生物学)
疾病
作者
Yan-Jie He,Pei-Ru Wei,Qiao-Yan Wu,Xin-Yu Zhang,Xing-mei Zhang,Xiao-Jia Liu,Fang Wang
出处
期刊:Journal of Southern Medical University
日期:2016-06-20
卷期号:36 (7): 904-8
被引量:1
摘要
To explore the relations among apolipoprotein E4, Tau protein and glycogen synthase kinase 3β (GSK-3β).U87 cells were transfected with pIRES-EGFP (control) or the recombinant plasmids ApoE4/pIRES-EGFP or ApoE3/pIRES-EGFP, and the expression levels of p-Tau/Tau and GSK-3β in the cells were examined with Western blotting. To further confirm the effect of ApoE on GSK-3β and p-Tau expressions, a short interfering RNA (siRNA) targeting ApoE (ApoE-siRNA) was transfected into U87 cells via Lipofectamine 2000 and the protein expressions were examined 24 h later.Compared with those in the control group, the expressions levels of both GSK-3β and p-Tau/Tau increased significantly in the cells transfected with ApoE4 and ApoE3 plasmids (P<0.01), and the ApoE4 plasmid produced a more potent effect than the ApoE3 plasmid on the protein expressions (P<0.01). ApoE knockdown resulted in significantly reduced expressions of GSK-3β (P<0.001) and p-Tau (P<0.01) in the cells.ApoE4 can enhance Tau phosphorylation though upregulating GSK-3β, which sheds light on a new role of ApoE4 in Alzheimer's disease.
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