Proteases and Proteolysis in Alzheimer Disease: A Multifactorial View on the Disease Process

被引:361
作者
De Strooper, Bart [1 ,2 ]
机构
[1] Katholieke Univ Leuven VIB, Ctr Human Genet, B-3000 Louvain, Belgium
[2] VIB, Dept Mol & Dev Genet, Louvain, Belgium
关键词
AMYLOID PRECURSOR PROTEIN; INSULIN-DEGRADING ENZYME; GAMMA-SECRETASE ACTIVITY; PAIRED HELICAL FILAMENTS; ANGIOTENSIN-CONVERTING ENZYME; APP TRANSGENIC MICE; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; NECROSIS-FACTOR-ALPHA; TRUNCATED A-BETA; TISSUE-PLASMINOGEN ACTIVATOR;
D O I
10.1152/physrev.00023.2009
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
De Strooper B. Proteases and Proteolysis in Alzheimer Disease: A Multifactorial View on the Disease Process. Physiol Rev 90: 465-494, 2010; doi:10.1152/physrev.00023.2009.-Alzheimer disease is characterized by the accumulation of abnormally folded protein fragments, i.e., amyloid beta peptide (A beta) and tau that precipitate in amyloid plaques and neuronal tangles, respectively. In this review we discuss the complicated proteolytic pathways that are responsible for the generation and clearance of these fragments, and how disturbances in these pathways interact and provide a background for a novel understanding of Alzheimer disease as a multifactorial disorder. Recent insights evolve from the static view that the morphologically defined plaques and tangles are disease driving towards a more dynamic, biochemical view in which the intermediary soluble A beta oligomers and soluble tau fragments are considered as the main mediators of neurotoxicity. The relevance of proteolytic pathways, centered on the generation and clearance of toxic A beta, on the cleavage and nucleation of tau, and on the general proteostasis of the neurons, then becomes obvious. Blocking or stimulating these pathways provide, or have the potential to provide, interesting drug targets, which raises the hope that we will be able to provide a cure for this dreadful disorder.
引用
收藏
页码:465 / 494
页数:30
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