A central role for astrocytes in the inflammatory response to β-amyloid;: chemokines, cytokines and reactive oxygen species are produced

被引:273
作者
Johnstone, M [1 ]
Gearing, AJH [1 ]
Miller, KM [1 ]
机构
[1] British Biotech Pharmaceut, Oxford OX4 5LY, England
关键词
Alzheimer's disease; beta-amyloid; astrocytes; microglia; chemokines; inflammation;
D O I
10.1016/S0165-5728(98)00226-4
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Alzheimer's disease (AD) is the commonest form of adult onset dementia and is characterised neuropathologically by the accumulation of plaques containing beta-amyloid (A beta) fibrils, reactive astrocytes, activated microglia, and leukocytes. A beta plays a role in the pathology of AD by directly causing neuronal cytotoxicity and stimulating microglia to secrete cytokines and reactive oxygen species (ROS) which also damage neurons. Here, we demonstrate that A beta activates astrocytes and oligodendrocytes (the most common cell types in the brain) to produce chemokines, in particular MCP-I and RANTES, which serve as potent in vitro microglial and macrophage chemoattractants. Furthermore, we have shown that A beta activates astrocytes to upregulate pro-inflammatory cytokine expression and enhances the production of ROS. We propose therefore that A beta-mediated astrocyte activation initiates an inflammatory cascade which could be targeted for therapeutic intervention in AD. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:182 / 193
页数:12
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