Dendritic spine loss in the hippocampus of young PDAPP and Tg2576 mice and its prevention by the ApoE2 genotype

• Published in: Neurobiology of disease 2003-08, Vol.13 (3), p.246-253
• Main Authors: Lanz, T.A, Carter, D.B, Merchant, K.M
• Format: Article
• Language: English
• Subjects: Age Factors; Alzheimer Disease - genetics; Alzheimer’s disease; Amyloid; Amyloid beta-Protein Precursor - genetics; Animals; apoE; Apolipoprotein E2; Apolipoproteins E - genetics; CA1; Dendrite; Dendrites - pathology; Genotype; Hippocampus; Hippocampus - pathology; Humans; Male; Mice; Mice, Transgenic; Models, Animal; Mutation; PDAPP; Plaque, Amyloid - pathology; Species Specificity; Synapse; Tg2576; Time Factors
• ISSN: 0969-9961; 1095-953X
• DOI: 10.1016/S0969-9961(03)00079-2

Postmortem AD brains exhibit dendritic spine loss in the hippocampus. To determine whether this pathology may be associated with amyloid burden, the present study used the Golgi stain technique to assess age- and genotype-dependent changes in dendritic spine density in CA1 hippocampus of two transgenic mouse lines that produce high levels of Aβ. Tg2576 and PDAPP mice, as well as a group of Tg2576 mice crossed with human apoE2-expressing transgenic mice, were compared to respective transgene-negative controls. Since the time course of amyloid plaque deposition in the PDAPP and Tg2576 mice is well characterized, we examined changes in spine density at ages that corresponded to different levels of amyloid plaque load. The data show age- and genotype-dependent reductions in spine density in both Tg2576 and PDAPP mice, albeit at somewhat different time courses. The spine loss occurred prior to plaque deposition and was ameliorated by the overexpression of human apoE2. These results suggest that a soluble Aβ species may affect hippocampal synapses and thereby contribute to functional deficits evident in these animals.