Alzheimer pathology disorganizes cortico-cortical circuitry: direct evidence from a transgenic animal model

被引:50
作者
Delatour, B
Blanchard, V
Pradier, L
Duyckaerts, C
机构
[1] Univ Paris 11, Lab Neurobiol Apprentissage Memoire & Commun, NAMC, CNRS,UMR 8620, F-91405 Orsay, France
[2] Univ Paris 06, Grp Hosp Pitie Salpetriere, Lab Neuropathol R Escourolle, INSERM,U289, F-75651 Paris, France
[3] Univ Paris 06, Grp Hosp Pitie Salpetriere, IFR Neurosci, F-75651 Paris, France
[4] Aventis Pharma, Neurodegenerat Dis Grp, Ctr Rech Paris, F-94403 Vitry Sur Seine, France
关键词
Alzheimer disease; connections; neurodegeneration; dystrophic neurites; amyloidosis; axonal tracing; cortex; transgenic mice; amyloid protein precursor; presenilin;
D O I
10.1016/j.nbd.2004.01.008
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
It has been proposed that Alzheimer disease (AD) is associated with a "disconnection syndrome" due to the gradual loss of morphological and functional integrity of cortico-cortical pathways. This hypothesis derives from indirect neuropathological observations, but definitive evidence that AD primarily targets cortico-cortical networks is still lacking. By means of neuroanatomical anterograde tracing methods, we have investigated, in a murine transgenic model of AD, the impact of the amyloid burden on axonal terminals in different neural systems. Axonal tracings revealed, in accordance with the "disconnection syndrome" hypothesis, that cortico-cortical fibers are significantly disorganized. Terminal fields in local and distant cortical areas contained numerous swollen dystrophic neurites often grouped in grape-like clusters at the plaque periphery. In contrary to fibers of cortical origin, those originating from subcortical brain structures only showed limited signs of degeneration upon reaching their cortical targets. These observations suggest a selective disruption of cortico-cortical connections induced by AD brain pathology. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:41 / 47
页数:7
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