Membrane Trafficking Pathways in Alzheimer's Disease

被引:148
|
作者
Rajendran, Lawrence [1 ]
Annaert, Wim [2 ,3 ]
机构
[1] Univ Zurich, Div Psychiat Res, CH-8008 Zurich, Switzerland
[2] Ctr Human Genet KULeuven, Lab Membrane Trafficking, B-3000 Louvain, Belgium
[3] VIB Ctr Biol Dis, B-3000 Louvain, Belgium
基金
瑞士国家科学基金会;
关键词
Alzheimer's disease; amyloid; APP; BACE; 1; endosomes; GWAS; lipid rafts; presenilin retromer; secretase; tau; AMYLOID PRECURSOR PROTEIN; GAMMA-SECRETASE COMPLEX; BETA-SECRETASE; A-BETA; ALPHA-SECRETASE; PRION PROTEIN; LIPID RAFTS; IN-VIVO; ENDOCYTIC TRAFFICKING; INTRACELLULAR DOMAIN;
D O I
10.1111/j.1600-0854.2012.01332.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Membrane proteins are constantly being trafficked in cells and the relevant proteins in Alzheimer's disease (AD), such as the amyloid precursor protein (APP) and its processing enzymes, are not exempted from that. Molecular cell biologists have been endeavoring to ascertain a roadmap for APP processing and trafficking in various cell types including neurons. This has led to the identification of numerous regulatory sorting mechanisms, proteinprotein interactions and lipidic microenvironments that largely define how and where the substrate APP meets its processing enzymes. However, the cell biology of tau, and the formation of neurofibrillary tangles, has long been regarded as a separate field. Nonetheless, recent progress is bringing both worlds together in a new paradigm on how A beta toxicity and tau are physiologically connected. Here, we discuss an update of our current appraisal on how membrane trafficking may play an important role in the pathogenesis of the disease and how this could be exploited for effective therapy.
引用
收藏
页码:759 / 770
页数:12
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