Neurogenesis in mouse models of Alzheimer's disease

被引:68
作者
Chuang, Tsu Tshen [1 ]
机构
[1] GlaxoSmithKline, Stem Cells DPU, Cambridge, MA 01139 USA
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2010年 / 1802卷 / 10期
关键词
Neural stem cell; Neurogenesis; Alzheimer's disease; Mouse model; Beta amyloid; Presenilin; AMYLOID-BETA-PEPTIDE; ADULT HIPPOCAMPAL NEUROGENESIS; NEURAL STEM-CELLS; A-BETA; PROGENITOR CELLS; SUBVENTRICULAR ZONE; PRECURSOR-PROTEIN; POSTNATAL NEUROGENESIS; SYNAPTIC PLASTICITY; COGNITIVE DEFICITS;
D O I
10.1016/j.bbadis.2009.12.008
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The brains of the adult mouse and human possess neural stem cells (NSCs) that retain the capacity to generate new neurons through the process of neurogenesis. They share the same anatomical locations of stem cell niches in the brain, as well as the prominent feature of rostral migratory stream formed by neuroblasts migrating from the lateral ventricles towards the olfactory bulb. Therefore the mouse possesses some fundamental features that may qualify it as a relevant model for adult human neurogenesis. Adult born young hippocampal neurons in the mouse display the unique property of enhanced plasticity, and can integrate physically and functionally into existing neural circuits in the brain. Such crucial properties of neurogenesis may at least partially underlie the improved learning and memory functions observed in the mouse when hippocampal neurogenesis is augmented, leading to the suggestion that neurogenesis induction may be a novel therapeutic approach for diseases with cognitive impairments such as Alzheimer's disease (AD). Research towards this goal has benefited significantly from the use of AD mouse models to facilitate the understanding in the impact of AD pathology on neurogenesis. The present article reviews the growing body of controversial data on altered neurogenesis in mouse models of AD and attempts to assess their relative relevance to humans. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:872 / 880
页数:9
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