Amyloid deposition in the hippocampus and entorhinal cortex

Quantitative analysis of a transgenic mouse model

John F. Reilly, Dora Games, Russell E. Rydel, Stephen Freedman, Dale Schenk, Warren G. Young, John Morrison, Floyd E. Bloom

Research output: Contribution to journalArticle

101 Citations (Scopus)

Abstract

Various transgenic mouse models of Alzheimer's disease (AD) have been developed that overexpress mutant forms of amyloid precursor protein in an effort to elucidate more fully the potential role of β-amyloid (Aβ) in the etiopathogenesis of the disease. The present study represents the first complete 3D reconstruction of Aβ in the hippocampus and entorhinal cortex of PDAPP transgenic mice. Aβ deposits were detected by immunostaining and thioflavin fluorescence, and quantified by using high-throughput digital image acquisition and analysis. Quantitative analysis of amyloid load in hippocampal subfields showed a dramatic increase between 12 and 15 months of age, with little or no earlier detectable deposition. Three-dimensional reconstruction in the oldest brains visualized previously unrecognized sheets of Aβ coursing through the hippocampus and cerebral cortex. In contrast with previous hypotheses, compact plaques form before significant deposition of diffuse Aβ, suggesting that different mechanisms are involved in the deposition of diffuse amyloid and the aggregation into plaques. The dentate gyrus was the hippocampal subfield with the greatest amyloid burden. Sublaminar distribution of Aβ in the dentate gyrus correlated most closely with the termination of afferent projections from the lateral entorhinal cortex, mirroring the selective vulnerability of this circuit in human AD. This detailed temporal and spatial analysis of Aβ and compact amyloid deposition suggests that specific corticocortical circuits express selective, but late, vulnerability to the pathognomonic markers of amyloid deposition, and can provide a basis for detecting prior vulnerability factors.

Original languageEnglish (US)
Pages (from-to)4837-4842
Number of pages6
JournalProceedings of the National Academy of Sciences of the United States of America
Volume100
Issue number8
DOIs
StatePublished - Apr 15 2003
Externally publishedYes

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Entorhinal Cortex
Amyloid
Transgenic Mice
Hippocampus
Dentate Gyrus
Alzheimer Disease
Spatio-Temporal Analysis
Amyloid beta-Protein Precursor
Cerebral Cortex
Fluorescence
Brain

ASJC Scopus subject areas

  • General

Cite this

Amyloid deposition in the hippocampus and entorhinal cortex : Quantitative analysis of a transgenic mouse model. / Reilly, John F.; Games, Dora; Rydel, Russell E.; Freedman, Stephen; Schenk, Dale; Young, Warren G.; Morrison, John; Bloom, Floyd E.

In: Proceedings of the National Academy of Sciences of the United States of America, Vol. 100, No. 8, 15.04.2003, p. 4837-4842.

Research output: Contribution to journalArticle

Reilly, John F. ; Games, Dora ; Rydel, Russell E. ; Freedman, Stephen ; Schenk, Dale ; Young, Warren G. ; Morrison, John ; Bloom, Floyd E. / Amyloid deposition in the hippocampus and entorhinal cortex : Quantitative analysis of a transgenic mouse model. In: Proceedings of the National Academy of Sciences of the United States of America. 2003 ; Vol. 100, No. 8. pp. 4837-4842.
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