Journal
ACTA NEUROPATHOLOGICA
Volume 100, Issue 5, Pages 451-458Publisher
SPRINGER-VERLAG
DOI: 10.1007/s004010000263
Keywords
amyloid precursor protein; Alzheimer's disease; apolipoprotein E; hippocampus; transgenic mice
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Funding
- NIA NIH HHS [K08 AG00793] Funding Source: Medline
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Apolipoprotein E (apoE) has been implicated as a risk factor for Alzheimer's disease and in the deposition, fibrillogenesis, and clearance of the amyloid beta-peptide (A beta). To examine the in vivo interactions between apoE and A beta deposition, we examined 12-month-old transgenic (tg) mice expressing human amyloid precursor protein (APP) with the V717F mutation (APP(V717F) homozygous) on an APOE null background. Elimination of APOE resulted in a redistribution and alteration in the character of A beta deposition in homozygous APP(V717F) 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 A beta deposition were not mediated by significant changes in regional APP expression, low-density lipoprotein receptor-related protein expression, or soluble A beta levels. Thus, apoE in APP(V717F) tg mice not only affects the amount and form of A beta deposition, but also the anatomical distribution of diffuse A beta deposits. The APP(V717F) tg mouse can serve as a model to investigate genetic influences on the vulnerability of specific neuroanatomical regions to A beta deposition.
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