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Title

Synaptic changes in the dentate gyrus of APP/PS1 transgenic mice revealed by electron microscopy

AuthorsAlonso-Nanclares, Lidia ; Merino-Serrais, Paula ; González, Santiago; DeFelipe, Javier
Issue Date2013
PublisherAmerican Association of Neuropathologists
CitationJournal of Neuropathology and Experimental Neurology 72: 386-395 (2013)
AbstractNumerous studies have reported widespread synaptic dysfunction or loss in early stages of both Alzheimer disease (AD) patients and animal models; it is widely accepted that synapse loss is the major structural correlate of cognitive dysfunction. Elucidation of the changes that may affect synapses is crucial for understanding the pathogenic mechanisms underlying AD, but ultrastructural preservation of human postmortem brain tissue is often poor, and classical methods for quantification of synapses have significant technical limitations. We previously observed changes in dendritic spines in plaque-free regions of the neuropil of the dentate gyrus of double-transgenic APP/PS1 (amyloid precursor protein/presenilin 1) model mice by light microscopy. Here, we used electron microscopy to examine possible synaptic alterations in this region. We used standard stereologic techniques to determine numbers of synapses per volume. We were able to reconstruct and analyze thousands of synapses and their 3-dimensional characteristics using a focused ion beam/scanning electron microscope and 3-dimensional reconstruction software (EspINA), which performs semiautomated segmentation of synapses. Our results show that both numbers of synapses per volume and synaptic morphology are affected in plaque-free regions of APP/PS1 mice. Therefore, changes in the number and morphology of synapses seem to be widespread alterations in this animal model. Copyright © 2013 by the American Association of Neuropathologists, Inc. Unauthorized reproduction of this article is prohibited.
URIhttp://hdl.handle.net/10261/80253
DOI10.1097/NEN.0b013e31828d41ec
Identifiersdoi: 10.1097/NEN.0b013e31828d41ec
issn: 0022-3069
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