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Título

3D Analysis of the Synaptic Organization in the Entorhinal Cortex in Alzheimer's Disease

AutorDomínguez-Álvaro, M.; Montero-Crespo, M. CSIC ORCID; Blázquez-Llorca, Lidia CSIC ORCID; Plaza-Alonso, Sergio CSIC ORCID; Cano-Astorga, Nicolás CSIC ORCID; DeFelipe, Javier CSIC ORCID ; Alonso-Nanclares, Lidia CSIC ORCID CVN
Palabras clavedementia
Electron microscopy
FIB/SEM
Medial temporal lobe
neuropil
postsynaptic targets
Fecha de publicación2021
EditorSociety for Neuroscience
CitacióneNeuro 8 (2021)
ResumenThe entorhinal cortex (EC) is especially vulnerable in the early stages of Alzheimer's disease (AD). In particular, cognitive deficits have been linked to alterations in the upper layers of EC. In the present report, we examined Layers II and III from eight human brain autopsies (four subjects with no recorded neurologic alterations and four AD cases). We used stereological methods to assess cortical atrophy of the EC and possible changes in the volume occupied by different cortical elements (neuronal and glial cell bodies; blood vessels; and neuropil). We performed 3D ultrastructural analyses of synapses using focused ion beam/scanning electron microscopy (FIB/SEM) to examine possible alterations related to AD. At the light microscope level, we found a significantly lower volume fraction occupied by neuronal bodies in Layer III and a higher volume fraction occupied by glial cell bodies in Layer II in AD cases. At the ultrastructural level, we observed that (1) there was a significantly lower synaptic density in both layers in AD cases; (2) synapses were larger and more complex in Layer II in AD cases; and (3) there was a greater proportion of small and simple synapses in Layer III in AD cases than in control individuals. These structural differences may play a role in the anatomic basis for the impairment of cognitive functions in AD.
Versión del editorhttp://dx.doi.org/10.1523/ENEURO.0504-20.2021
URIhttp://hdl.handle.net/10261/249302
DOI10.1523/ENEURO.0504-20.2021
Identificadoresdoi: 10.1523/ENEURO.0504-20.2021
issn: 2373-2822
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