Wilson Christina A, Doms Robert W, Zheng Hui, Lee Virginia M-Y
Center for Neurodegenerative Disease Research, Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
Nat Neurosci. 2002 Sep;5(9):849-55. doi: 10.1038/nn898.
Presenilins 1 and 2 (PS1/PS2) have been suggested to be gamma-secretases responsible for the proteolytic cleavage of amyloid precursor protein (APP) to form amyloid-beta (A beta), a protein implicated in the development of Alzheimer's disease. Here we examined whether these presenilins are required for the generation of multiple A beta species by analyzing the production of several forms of secreted and intracellular A beta in mouse cells lacking PS1, PS2 or both proteins. Although most A beta species were abolished in PS1/PS2(-/-) cells, the production of intracellular A beta 42 generated in the endoplasmic reticulum/intermediate compartment was unaffected by the absence of these proteins, either singly or in combination. These results indicate that production of this pool of A beta occurs independently of PS1/PS2, and therefore, another gamma-secretase activity must be responsible for cleavage of APP within the early secretory compartments.
早老素1和2(PS1/PS2)被认为是γ-分泌酶,负责将淀粉样前体蛋白(APP)进行蛋白水解切割,以形成β淀粉样蛋白(Aβ),该蛋白与阿尔茨海默病的发展有关。在此,我们通过分析缺乏PS1、PS2或这两种蛋白的小鼠细胞中几种分泌型和细胞内Aβ形式的产生情况,来研究这些早老素是否是产生多种Aβ物种所必需的。尽管在PS1/PS2(-/-)细胞中大多数Aβ物种被消除,但在内质网/中间区室中产生的细胞内Aβ42的产生不受这些蛋白单独或联合缺失的影响。这些结果表明,这一Aβ池的产生独立于PS1/PS2,因此,另一种γ-分泌酶活性必定负责在早期分泌区室中对APP的切割。