The Role of Apolipoprotein E Isoforms in Alzheimer's Disease

被引:25
|
作者
Roda, Alejandro R. [1 ]
Montoliu-Gaya, Laia [1 ,2 ]
Villegas, Sandra [1 ]
机构
[1] Univ Autonoma Barcelona, Dept Bioquim & Biol Mol, Fac Biociencies, Prot Design & Immunotherapy Grp, E-08193 Barcelona, Spain
[2] Univ Gothenburg, Inst Biomed, Dept Clin Chem & Transfus Med, Gothenburg, Sweden
关键词
A beta clearance; A beta aggregation; A beta PP transcription; AICD generation; Alzheimer's disease; amyloid-beta; apolipoprotein E; lipid metabolism; mitochondrial damage; neuroinflammation; GENOME-WIDE ASSOCIATION; CENTRAL-NERVOUS-SYSTEM; DORSAL RAPHE NUCLEUS; AMYLOID-BETA; A-BETA; MOUSE MODEL; SYNAPTIC PLASTICITY; POSTERIOR CINGULATE; IDENTIFIES VARIANTS; SIGNALING PROTEINS;
D O I
10.3233/JAD-180740
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Alzheimer's disease (AD), the most common type of dementia worldwide, is characterized by high levels of amyloid-beta (A beta) peptide and hyperphosphorylated tau protein. Genetically, the epsilon 4 allele of apolipoprotein E (ApoE) has been established as the major risk factor for developing late-onset AD (LOAD), the most common form of the disease. Although the role ApoE plays in AD is still not completely understood, a differential role of its isoforms has long been known. The current review compiles the involvement of ApoE isoforms in amyloid-beta protein precursor transcription, A beta aggregation and clearance, synaptic plasticity, neuroinflammation, lipid metabolism, mitochondrial function, and tau hyperphosphorylation. Due to the complexity of LOAD, an accurate description of the interdependence among all the related molecular mechanisms involved in the disease is needed for developing successful therapies.
引用
收藏
页码:459 / 471
页数:13
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