Aβ-independent roles of apolipoprotein E4 in the pathogenesis of Alzheimer's disease

被引:133
|
作者
Huang, Yadong [1 ,2 ,3 ]
机构
[1] Univ Calif San Francisco, Gladstone Inst Neurol Dis, Gladstone Inst Cardiovasc Dis, San Francisco, CA 94158 USA
[2] Univ Calif San Francisco, Dept Pathol, San Francisco, CA 94158 USA
[3] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94158 USA
关键词
CENTRAL-NERVOUS-SYSTEM; INCREASED TAU PHOSPHORYLATION; CEREBRAL GLUCOSE-METABOLISM; TRAUMATIC BRAIN-INJURY; APOE EPSILON-4 ALLELE; TRANSGENIC MICE; NEURITE OUTGROWTH; DOMAIN INTERACTION; NEUROFIBRILLARY TANGLES; CHOLESTEROL TRANSPORT;
D O I
10.1016/j.molmed.2010.04.004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human apolipoprotein (APO) E has three common isoforms that differentially affect lipid and neuronal homeotasis. APOE4, the major known genetic risk factor for Alzheimer's disease (AD), increases the occurrence and lowers the age of onset of AD. APOE4 carriers account or 65-80% of all AD cases, highlighting the importance f APOE4 in AD pathogenesis. Emerging data suggest hat APOE4 contributes to AD through various path-ways, some of which are dependent on amyloid-beta A beta). Although these A beta-dependent roles of APOE4 have seen widely studied, APOE4 has detrimental effects on eurons independent of A beta: aberrant proteolysis of APOE4 generates neurotoxic fragments, stimulates au phosphorylation, which disrupts the cytoskeleton, nd impairs mitochondrial function.
引用
收藏
页码:287 / 294
页数:8
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