LRP1型
淀粉样前体蛋白
α分泌酶
内化
劈理(地质)
免疫沉淀
淀粉样前体蛋白分泌酶
P3肽
细胞生物学
化学
老年斑
受体
生物
阿尔茨海默病
生物化学
基因
低密度脂蛋白受体
医学
内科学
胆固醇
古生物学
断裂(地质)
疾病
脂蛋白
作者
Bjoern von Einem,Daniel Schwanzar,Florian Rehn,Annika Beyer,Petra Weber,Michael Wagner,Herbert Schneckenburger,Christine A. F. Von Arnim
标识
DOI:10.1016/j.expneurol.2010.05.017
摘要
Cleavage of APP by BACE1 is the first proteolytic step in the production of amyloid-beta (Aβ), which accumulates in senile plaques in Alzheimer's disease. Through its interaction with APP, the low-density receptor-related protein 1 (LRP1) enhances APP internalization. Recently, BACE1 has been shown to interact with and cleave the light chain (lc) of LRP1. Since LRP1 is known to compete with APP for cleavage by gamma-secretase, we tested the hypothesis that LRP1 also acts as a competitive substrate for β-secretase. We found that the increase in secreted APP (sAPP) mediated by over-expression of BACE1 in APP-transfected cells could be decreased by simultaneous LRP1 over-expression. Analysis by multi-spot ELISA revealed that this is due to a decrease in sAPPβ, but not sAPPα. Interaction between APP and BACE1, as measured by immunoprecipitation and fluorescence lifetime assays, was impaired by LRP1 over-expression. We also demonstrate that APP over-expression leads to decreased LRP1 association with and cleavage by BACE1. In conclusion, our data suggest that – in addition to its role in APP trafficking – LRP1 affects APP processing by competing for cleavage by BACE1.
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