The spatial pattern of discrete beta-amyloid deposits in Alzheimer's disease reflects synaptic disconnection.

R A Armstrong
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引用次数: 17

Abstract

The spatial pattern of discrete beta-amyloid (A beta) deposits was studied in the superficial laminae of cortical fields of different types and in the hippocampus in 6 cases of Alzheimer's disease (AD). In 41/42 tissues examined, discrete A beta deposits were aggregated into clusters and in 34/41 tissues (25/34 of the cortical tissues), there was evidence for a regular periodicity of the A beta deposit clusters parallel to the tissue boundary. The dimensions of the clusters varied from 400 to > 12,800 microns in different tissues. Although the A beta deposit clusters were larger than predicted, the regular periodicity suggests that they develop in relation to groups of cells associated with specific projections. This would be consistent with the hypothesis that the distribution of discrete A beta deposits in AD could reflect progressive synaptic disconnection along interconnected neuronal pathways. This implies that amyloid deposition could be a response to, rather than a cause of, synaptic disconnection in AD.
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阿尔茨海默病中离散的β -淀粉样蛋白沉积的空间模式反映了突触的断开。
本文研究了6例阿尔茨海默病(AD)不同类型皮质区浅层和海马中离散β -淀粉样蛋白(A β)沉积的空间格局。在41/42个被检查的组织中,离散的A - β沉积聚集成簇,在34/41个组织(25/34的皮质组织)中,有证据表明平行于组织边界的A - β沉积簇有规律的周期性。在不同的组织中,簇的尺寸从400微米到> 12,800微米不等。尽管A β沉积簇比预测的要大,但规律的周期性表明它们是与特定突起相关的细胞群相关的。这与一种假设是一致的,即阿尔茨海默病中离散A β沉积的分布可能反映了沿相互连接的神经元通路的进行性突触断开。这意味着淀粉样蛋白沉积可能是对阿尔茨海默病突触断开的反应,而不是原因。
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