Wirths Oliver, Bayer Thomas A
Division of Molecular Psychiatry and Alzheimer Ph.D. Graduate School, Department of Psychiatry, University of Goettingen, von-Siebold-Str. 5, 37075 Goettingen, Germany.
Int J Alzheimers Dis. 2010 Aug 12;2010:723782. doi: 10.4061/2010/723782.
Since their initial generation in the mid 1990s, transgenic mouse models of Alzheimers's disease (AD) have been proven to be valuable model systems which are indispensable for modern AD research. Whereas most of these models are characterized by extensive amyloid plaque pathology, inflammatory changes and often behavioral deficits, modeling of neuron loss was much less successful. The present paper discusses the current achievements of modeling neuron loss in transgenic mouse models based on APP/Aβ and Tau overexpression and provides an overview of currently available AD mouse models showing these pathological alterations.
自20世纪90年代中期首次产生以来,阿尔茨海默病(AD)转基因小鼠模型已被证明是现代AD研究不可或缺的有价值的模型系统。尽管这些模型大多具有广泛的淀粉样斑块病理、炎症变化且常常伴有行为缺陷,但神经元丢失的建模却不太成功。本文讨论了基于APP/Aβ和Tau过表达的转基因小鼠模型在神经元丢失建模方面的当前成果,并概述了目前显示这些病理改变的可用AD小鼠模型。