Aβ-Degrading Proteases: Therapeutic Potential in Alzheimer Disease

被引:0
|
作者
Malcolm A. Leissring
机构
[1] University of California,Institute for Memory Impairments and Neurological Disorders (UCI MIND)
来源
CNS Drugs | 2016年 / 30卷
关键词
Alzheimer Disease; Amyloid Precursor Protein; Amyloid Precursor Protein Gene; Alzheimer Disease Case; Alzheimer Disease Pathogenesis;
D O I
暂无
中图分类号
学科分类号
摘要
The amyloid β-protein (Aβ) plays an indispensable role in the pathogenesis of Alzheimer disease (AD). Aβ is subject to proteolytic degradation by a diverse array of peptidases and proteinases, known collectively as Aβ-degrading proteases (AβDPs). A growing number of AβDPs have been identified that impact Aβ powerfully and in a surprising variety of ways. As such, AβDPs hold considerable therapeutic potential for the treatment and/or prevention of AD. Here, we critically review the relative merits of therapeutic strategies targeting AβDPs compared with current Aβ-lowering strategies focused on immunotherapies and pharmacological modulation of Aβ-producing enzymes. Several innovative advances have increased considerably the feasibility of delivering AβDPs to the brain or enhancing their activity in a non-invasive manner. We argue that therapies targeting AβDPs offer numerous potential advantages that should be explored through continued research into this promising field.
引用
收藏
页码:667 / 675
页数:8
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