期刊
CURRENT ALZHEIMER RESEARCH
卷 12, 期 1, 页码 32-46出版社
BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1567205012666141218140953
关键词
Alzheimer's disease; amyloid beta degradation; amyloid beta peptide; endothelin-converting enzyme; insulin-degrading enzyme; neprilysin; neurodegeneration
资金
- Alzheimer Association IIRG [10-173-180]
- Alzheimer Association NIH [AG046200, AG042804]
- Alzheimer's Association [IIRG-11-206418]
- NIA
- MSTP grant [NIH T32 GM08716-13]
Amyloid-beta proteins (A beta) of 42 (A beta 42) and 40 aa (A beta 40) accumulate as senile plaques (SP) and cerebrovascular amyloid protein deposits that are defining diagnostic features of Alzheimer's disease (AD). A number of rare mutations linked to familial AD (FAD) on the A beta precursor protein (APP), Presenilin-1 (PS1), Presenilin-2 (PS2), Adamalysin10, and other genetic risk factors for sporadic AD such as the epsilon 4 allele of Apolipoprotein E (ApoE-epsilon 4) foster the accumulation of A beta and also induce the entire spectrum of pathology associated with the disease. A beta accumulation is therefore a key pathological event and a prime target for the prevention and treatment of AD. APP is sequentially processed by beta-site APP cleaving enzyme (BACE1) and gamma-secretase, a multisubunit PS1/PS2-containing integral membrane protease, to generate A beta. Although A beta accumulates in all forms of AD, the only pathways known to be affected in FAD increase A beta production by APP gene duplication or via base substitutions on APP and gamma-secretase subunits PS1 and PS2 that either specifically increase the yield of the longer A beta 42 or both A beta 40 and A beta 42. However, the vast majority of AD patients accumulate A beta without these known mutations. This led to proposals that impairment of A beta degradation or clearance may play a key role in AD pathogenesis. Several candidate enzymes, including Insulin-degrading enzyme (IDE), Neprilysin (NEP), Endothelin-converting enzyme (ECE), Angiotensin converting enzyme (ACE), Plasmin, and Matrix metalloproteinases (MMPs) have been identified and some have even been successfully evaluated in animal models. Several studies also have demonstrated the capacity of gamma-secretase inhibitors to paradoxically increase the yield of A beta and we have recently established that the mechanism is by skirting A beta degradation. This review outlines major cellular pathways of A beta degradation to provide a basis for future efforts to fully characterize the panel of pathways responsible for A beta turnover.
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