Center for Dementia Research, Nathan Kline Institute, Orangeburg, NY 10962, USA.
Proc Natl Acad Sci U S A. 2010 Jan 26;107(4):1630-5. doi: 10.1073/pnas.0908953107. Epub 2009 Dec 28.
An additional copy of the beta-amyloid precursor protein (APP) gene causes early-onset Alzheimer's disease (AD) in trisomy 21 (DS). Endosome dysfunction develops very early in DS and AD and has been implicated in the mechanism of neurodegeneration. Here, we show that morphological and functional endocytic abnormalities in fibroblasts from individuals with DS are reversed by lowering the expression of APP or beta-APP-cleaving enzyme 1 (BACE-1) using short hairpin RNA constructs. By contrast, endosomal pathology can be induced in normal disomic (2N) fibroblasts by overexpressing APP or the C-terminal APP fragment generated by BACE-1 (betaCTF), all of which elevate the levels of betaCTFs. Expression of a mutant form of APP that cannot undergo beta-cleavage had no effect on endosomes. Pharmacological inhibition of APP gamma-secretase, which markedly reduced Abeta production but raised betaCTF levels, also induced AD-like endosome dysfunction in 2N fibroblasts and worsened this pathology in DS fibroblasts. These findings strongly implicate APP and the betaCTF of APP, and exclude Abeta and the alphaCTF, as the cause of endocytic pathway dysfunction in DS and AD, underscoring the potential multifaceted value of BACE-1 inhibition in AD therapeutics.
额外的β-淀粉样前体蛋白(APP)基因拷贝导致三体 21(DS)中的早发性阿尔茨海默病(AD)。内体功能障碍在 DS 和 AD 中很早就出现,并与神经退行性变的机制有关。在这里,我们表明,使用短发夹 RNA 构建体降低 APP 或β-淀粉样前体蛋白切割酶 1(BACE-1)的表达,可以逆转 DS 个体成纤维细胞中的形态和功能内吞异常。相比之下,通过过表达 APP 或由 BACE-1(βCTF)产生的 APP 的 C 末端片段,可以在正常二倍体(2N)成纤维细胞中诱导内体病理学,所有这些都增加了βCTFs 的水平。表达不能进行β切割的 APP 突变体形式对内体没有影响。APP γ-分泌酶的药理学抑制显著减少了 Abeta 的产生,但增加了βCTF 水平,也在内 2N 成纤维细胞中诱导出类似 AD 的内体功能障碍,并在 DS 成纤维细胞中加重了这种病理学。这些发现强烈暗示 APP 和 APP 的βCTF,以及排除 Abeta 和αCTF,是 DS 和 AD 中内吞途径功能障碍的原因,突出了 BACE-1 抑制在 AD 治疗中的潜在多方面价值。