Evidence for glial-mediated inflammation in aged APPSW transgenic mice

被引:255
作者
Benzing, WC [1 ]
Wujek, JR
Ward, EK
Shaffer, D
Ashe, KH
Younkin, SG
Brunden, KR
机构
[1] Gliatech Inc, Cleveland, OH 44122 USA
[2] Univ Minnesota, Dept Neurol, Minneapolis, MN 55455 USA
[3] Mayo Clin Jacksonville, Jacksonville, FL 32224 USA
关键词
Alzheimer's disease; animal model; cytokine; glia; IL-1; beta; IL-6; immunocytochemistry; inflammation; mouse; transgenic; TNF;
D O I
10.1016/S0197-4580(99)00065-2
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
Chronic expression of inflammatory cytokines, including interleukin-1 beta, tumor necrosis factor alpha, and interleukin-6, by glia may underlie the neurodegenerative events that occur within the brains of patients with Alzheimer's disease (AD). The present study determined whether these markers of inflammation could be observed within the brains of Te(HuAPP695.K670N/M67 1L)2576 transgenic mice (Tg2576) that have recently been shown to mimic many features of AD. Interleukin-1 beta- and turner necrosis factor alpha-immunopositive microglia were localized with thioflavine-positive (fibrillar) A beta deposits. Moreover, interleukin-6 immunoreactive astrocytes surrounded fibrillar A beta deposits. These findings provide evidence that Tg2516 mice exhibit features of the inflammatory pathology seen in AD and suggest that these mice are a useful animal model for studying the role inflammation may play in this disease. (C) 2000 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:581 / 589
页数:9
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