ApoE Lipidation as a Therapeutic Target in Alzheimer's Disease

被引:102
|
作者
Lanfranco, Maria Fe [1 ]
Ng, Christi Anne [1 ]
Rebeck, G. William [1 ]
机构
[1] Georgetown Univ, Dept Neurosci, Med Ctr, 3970 Reservoir Rd NW, Washington, DC 20057 USA
关键词
apolipoprotein E; cholesterol; lipid homeostasis; neurodegeneration; HUMAN APOLIPOPROTEIN-E; CENTRAL-NERVOUS-SYSTEM; CHOLESTEROL BIOSYNTHETIC-PATHWAY; LDL RECEPTOR-BINDING; LIVER-X-RECEPTOR; AMYLOID-BETA; MOUSE MODEL; CEREBROSPINAL-FLUID; E GENOTYPE; IN-VITRO;
D O I
10.3390/ijms21176336
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
Apolipoprotein E (APOE) is the major cholesterol carrier in the brain, affecting various normal cellular processes including neuronal growth, repair and remodeling of membranes, synaptogenesis, clearance and degradation of amyloid beta (A beta) and neuroinflammation. In humans, theAPOEgene has three common allelic variants, termed E2, E3, and E4.APOE4is considered the strongest genetic risk factor for Alzheimer's disease (AD), whereasAPOE2is neuroprotective. To perform its normal functions, apoE must be secreted and properly lipidated, a process influenced by the structural differences associated with apoE isoforms. Here we highlight the importance of lipidated apoE as well as theAPOE-lipidation targeted therapeutic approaches that have the potential to correct or prevent neurodegeneration. Many of these approaches have been validated using diverse cellular and animal models. Overall, there is great potential to improve the lipidated state of apoE with the goal of amelioratingAPOE-associated central nervous system impairments.
引用
收藏
页码:1 / 19
页数:19
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