NEUROINFLAMMATION IN ALZHEIMER'S DISEASE; A SOURCE OF HETEROGENEITY AND TARGET FOR PERSONALIZED THERAPY

被引:135
|
作者
Latta, C. H. [1 ,2 ]
Brothers, H. M. [1 ]
Wilcock, D. M. [1 ]
机构
[1] Univ Kentucky, Sanders Brown Ctr Aging, Dept Physiol, Lexington, KY 40536 USA
[2] Univ Manchester, Dept Biol, Manchester M13 9PL, Lancs, England
关键词
microglia; amyloid; Alzheimer's; cytokines; phenotypes; inflammation; CENTRAL-NERVOUS-SYSTEM; ANTIINFLAMMATORY PREVENTION TRIAL; RANDOMIZED CONTROLLED-TRIAL; APP+PS1 TRANSGENIC MICE; MACROPHAGE ACTIVATION; A-BETA; ALTERNATIVE ACTIVATION; DOUBLE-BLIND; IMMUNOHISTOCHEMICAL LOCALIZATION; MICROGLIAL ACTIVATION;
D O I
10.1016/j.neuroscience.2014.09.061
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neuroinflammation has long been known as an accompanying pathology of Alzheimer's disease. Microglia surrounding amyloid plaques in the brain of Auguste D were described in the original publication of Alois Alzheimer. It is only quite recently, however, that we have a more complete appreciation for the diverse roles of neuroinflammation in neurodegenerative disorders such as Alzheimer's. While gaps in our knowledge remain, and conflicting data are abound in the field, our understanding of the complexities and heterogeneous functions of the inflammatory response in Alzheimer's is vastly improved. This review article will discuss some of the roles of neuroinflammation in Alzheimer's disease, in particular, how understanding heterogeneity in the individual inflammatory response can be used in therapeutic development and as a mechanism of personalizing our treatment of the disease. (C) 2014 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:103 / 111
页数:9
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