Intracellular Aβ triggers neuron loss in the cholinergic system of the APP/PS1KI mouse model of Alzheimer's disease

被引:65
作者
Christensen, Ditte Z.
Bayer, Thomas A.
Wirths, Oliver [1 ]
机构
[1] Univ Gottingen, Div Mol Psychiat, D-37075 Gottingen, Germany
关键词
Alzheimer; Amyloid; Pathology; Acetylcholine; Intraneuronal abeta; Transgenic mice; Motor nuclei; AMYLOID PRECURSOR PROTEIN; TRANSGENIC MICE; SELECTIVE LOSS; HIPPOCAMPUS; APP; NEUROPATHOLOGY; ACCUMULATION; DEGENERATION; MODULATION; HYPOTHESIS;
D O I
10.1016/j.neurobiolaging.2008.07.022
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
Loss of cholinergic neurons in the Nucleus Basalis of Meynert in Alzheimer's disease (AD) patients was one of the first discoveries of neuron loss in AD. Despite an intense focus on the cholinergic system in AD, the reason for this cholinergic neuron loss is yet unknown. In the present study we examined A beta-induced pathology and neuron loss in the cholinergic system of the bigenic APP/PS1KI mouse model. Expression of the APP transgene was found in ChAT-positive neurons of motor nuclei accompanied by robust intracellular A beta accumulation, whereas no APP expressing neurons and thus no intracellular A beta accumulation were found in neither the forebrain or pons complexes, nor in the caudate putamen. This expression pattern was used as a model system to study the effect of intra- and extracellular A beta accumulation on neuron loss in the cholinergic system. Stereological quantification revealed a loss of ChAT-positive neurons in APP/PS1KI mice only in the motor nuclei Mo5 and 7N accumulating intracellular A beta. This study supports the hypothesis of intracellular A beta accumulation as an early pathological alteration contributing to cell death in AD. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:1153 / 1163
页数:11
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