期刊
JOURNAL OF NEUROCHEMISTRY
卷 116, 期 1, 页码 10-21出版社
WILEY-BLACKWELL PUBLISHING, INC
DOI: 10.1111/j.1471-4159.2010.07081.x
关键词
Alzheimer's disease; ADAM proteases; ectodomain shedding; metalloproteases; regulated intramembrane proteolysis; sirtuins
资金
- Deutsche Forschungsgemeinschaft [SFB596, TP B12]
- BMBF (KNDD)
P>Ectodomain shedding of the amyloid precursor protein (APP) by the metalloprotease activity alpha-secretase is a key regulatory event preventing the generation of the Alzheimer's disease (AD) amyloid beta peptide. Proteases similar to alpha-secretase are essential for diverse physiological processes, such as embryonic development, cell adhesion and neuronal guidance. Previously, several proteases were suggested as candidate alpha-secretases for APP, in particular members of the ADAM family (a disintegrin and metalloprotease). Two recent studies analyzed primary neurons, which are the cell type affected in AD, and finally demonstrated that the constitutively cleaving alpha-secretase activity is selectively mediated by ADAM10. An increase in alpha-secretase cleavage is considered a therapeutic approach for AD. However, the molecular mechanisms regulating alpha-secretase cleavage remain only partly understood. Signaling pathways activating protein kinase C and MAP kinase play a central role in stimulating alpha-secretase cleavage of APP. Additionally, several recent publications demonstrate that ADAM10 expression and alpha-secretase cleavage of APP are tightly controlled at the level of transcription, e.g. by retinoic acid receptors and sirtuins, and at the level of translation and protein trafficking. This review focuses on the recent progress made in unraveling the molecular identity, regulation and therapeutic potential of alpha-secretase in Alzheimer's disease.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据