Abstract
Apolipoprotein E (apoE) has been implicated as a risk factor for Alzheimer’s disease and in the deposition, fibrillogenesis, and clearance of the amyloid β-peptide (Aβ). To examine the in vivo interactions between apoE and Aβ deposition, we examined 12-month-old transgenic (tg) mice expressing human amyloid precursor protein (APP) with the V717F mutation (APPV717F homozygous) on an APOE null background. Elimination of APOE resulted in a redistribution and alteration in the character of Aβ deposition in homozygous APPV717F tg mice, with a dramatic reduction in cortical and dentate gyrus deposition, prominent increase in diffuse CA1 and CA3 deposition, and prevention of the formation of thioflavin-S-positive deposits. These alterations in Aβ deposition were not mediated by significant changes in regional APP expression, low-density lipoprotein receptor-related protein expression, or soluble Aβ levels. Thus, apoE in APPV717F tg mice not only affects the amount and form of Aβ deposition, but also the anatomical distribution of diffuse Aβ deposits. The APPV717F tg mouse can serve as a model to investigate genetic influences on the vulnerability of specific neuroanatomical regions to Aβ deposition.
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Received: 11 April 2000 / Revised, accepted: 25 May 2000
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Irizarry, M., Cheung, B., Rebeck, G. et al. Apolipoprotein E affects the amount, form, and anatomical distribution of amyloid β-peptide deposition in homozygous APPV717F transgenic mice. Acta Neuropathol 100, 451–458 (2000). https://doi.org/10.1007/s004010000263
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DOI: https://doi.org/10.1007/s004010000263