Literature DB >> 24055684

Synaptic deficits in layer 5 neurons precede overt structural decay in 5xFAD mice.

Y Buskila1, S E Crowe, G C R Ellis-Davies.   

Abstract

Synaptic decay and neurodegeneration are hallmarks of Alzheimer's disease that are thought to precede dementia. Recently, we have reported that the first signs of neuritic dystrophy in a new transgenic mouse model of familial Alzheimer's disease (FAD) called the "5xFAD" are axonal dystrophy followed by loss of spines on basal dendrites. The 5xFAD mouse has profound loss of layer 5 neurons by 12months, and these initial structural insults appear between 4 and 6months of age. Here, we test, for the first time, if synaptic failure of layer 5 neurons in the 5xFAD mouse precedes these structural changes. We used longitudinal, in vivo two-photon fluorescence imaging of bigenic 5xFAD/YFP mice to assess the overall structural stability of layer 5 neurons in young mice (age less than 14weeks). We found these neurons to be structurally and morphologically sound. In parallel, we used in vitro, whole-cell patch clamp electrophysiology of layer 5 pyramidal neurons, from mice aged 8-12weeks, to reveal significant pre- and postsynaptic defects in these cells. Thus our data suggest that layer 5 neurons in the 5xFAD mouse model have synaptic deficits at an early time point, before any overt structural dystrophy, and that such synaptic failure, with co-temporal biochemical changes, may be an early step in neuronal loss.
Copyright © 2013 IBRO. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  5xFAD; EGTA; FAD; HEPES; PPR; RMP; STDP; WT; aCSF; artificial cerebrospinal fluid; ethylene glycol tetraacetic acid; familial Alzheimer’s disease; hydroxyethyl piperazineethanesulfonic acid; in vivo imaging; mEPSCs; miniature excitatory post-synaptic currents; paired-pulse ratio; resting membrane potential; spike-timing-dependent plasticity; synaptic failure; wild type

Mesh:

Year:  2013        PMID: 24055684      PMCID: PMC4078998          DOI: 10.1016/j.neuroscience.2013.09.016

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


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