Department of Neurology, Affiliated Nanhua Hospital, University of South China, Hengyang, Hunan 421001, China.
Department of Neurology, Affiliated Nanhua Hospital, University of South China, Hengyang, Hunan 421001, China.
Life Sci. 2020 Apr 1;246:117430. doi: 10.1016/j.lfs.2020.117430. Epub 2020 Feb 18.
Angiopoietin-1 (Ang-1), a regulatory angiogenesis protein and it has been found to be involved in the occurrence and progression of Alzheimer's disease. However, it was still to be addressed the distinctly role and the molecular mechanisms of Ang-1 affects Alzheimer's disease. Our data suggest that Ang-1 aggravated the accumulation of Aβ and cognitive decline in APP/PS1 mice. The upregulation of APPβ is essential for Aβ production in N2a cells overexpressing the mutational human APP gene (N2a/APP695 cells), while downregulation of PEN2 could reduce APP expression. Silencing of FOXA2 lead to inhibition of APP expression, as well as decrease of Aβ contents. In conclusion, Ang-1 has an accelerative effect on Alzheimer's disease by increasing the secretion of Aβ via FOXA2/PEN2/APP pathway.
血管生成素-1(Ang-1)是一种调节血管生成的蛋白,它已被发现与阿尔茨海默病的发生和发展有关。然而,Ang-1 影响阿尔茨海默病的明确作用和分子机制仍有待解决。我们的数据表明,Ang-1 加重了 APP/PS1 小鼠中 Aβ 的积累和认知能力下降。在过表达突变型人 APP 基因的 N2a 细胞(N2a/APP695 细胞)中,APPβ 的上调对于 Aβ 的产生是必不可少的,而 PEN2 的下调可以减少 APP 的表达。FOXA2 的沉默导致 APP 表达的抑制,以及 Aβ 含量的降低。总之,Ang-1 通过 FOXA2/PEN2/APP 途径增加 Aβ 的分泌,对阿尔茨海默病有加速作用。