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Publication : Reducing human apolipoprotein E levels attenuates age-dependent Aβ accumulation in mutant human amyloid precursor protein transgenic mice.

First Author  Bien-Ly N Year  2012
Journal  J Neurosci Volume  32
Issue  14 Pages  4803-11
PubMed ID  22492035 Mgi Jnum  J:184138
Mgi Id  MGI:5320350 Doi  10.1523/JNEUROSCI.0033-12.2012
Citation  Bien-Ly N, et al. (2012) Reducing human apolipoprotein E levels attenuates age-dependent Abeta accumulation in mutant human amyloid precursor protein transgenic mice. J Neurosci 32(14):4803-11
abstractText  Apolipoprotein E4 (apoE4) plays a major role in the pathogenesis of Alzheimer's disease. Brain amyloid-beta (Abeta) accumulation depends on age and apoE isoforms (apoE4 > apoE3) both in humans and in transgenic mouse models. Brain apoE levels are also isoform dependent, but in the opposite direction (apoE4 < apoE3). Thus, one prevailing hypothesis is to increase brain apoE expression to reduce Abeta levels. To test this hypothesis, we generated mutant human amyloid precursor protein transgenic mice expressing one or two copies of the human APOE3 or APOE4 gene that was knocked in and flanked by LoxP sites. We report that reducing apoE3 or apoE4 expression by 50% in 6-month-old mice results in efficient Abeta clearance and does not increase Abeta accumulation. However, 12-month-old mice with one copy of the human APOE gene had significantly reduced Abeta levels and plaque loads compared with mice with two copies, regardless of which human apoE isoform was expressed, suggesting a gene dose-dependent effect of apoE on Abeta accumulation in aged mice. Additionally, 12-month-old mice expressing one or two copies of the human APOE4 gene had significantly higher levels of Abeta accumulation and plaque loads than age-matched mice expressing one or two copies of the human APOE3 gene, suggesting an isoform-dependent effect of apoE on Abeta accumulation in aged mice. Moreover, Cre-mediated APOE4 gene excision in hippocampal astrocytes significantly reduced insoluble Abeta in adult mice. Thus, reducing, rather than increasing, apoE expression is an attractive approach to lowering brain Abeta levels.
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