Do Microglia Default on Network Maintenance in Alzheimer's Disease?

被引:17
|
作者
Southam, Katherine A. [1 ]
Vincent, Adele J. [1 ]
Small, David H. [1 ]
机构
[1] Univ Tasmania, Menzies Inst Med Res, 17 Liverpool St, Hobart, Tas 7000, Australia
基金
英国医学研究理事会; 澳大利亚国家健康与医学研究理事会;
关键词
Microglia; network abnormalities; neural networks; phagocytosis; synapse pruning; CENTRAL-NERVOUS-SYSTEM; AMYLOID-BETA-PEPTIDE; MILD COGNITIVE IMPAIRMENT; GENOME-WIDE ASSOCIATION; APOLIPOPROTEIN-E; IN-VIVO; SYNAPTIC PLASTICITY; IDENTIFIES VARIANTS; NEUROTROPHIC FACTOR; IMAGING BIOMARKERS;
D O I
10.3233/JAD-151075
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Although the cause of Alzheimer's disease (AD) remains unknown, a number of new findings suggest that the immune system may play a critical role in the early stages of the disease. Genome-wide association studies have identified a wide array of risk-associated genes for AD, many of which are associated with abnormal functioning of immune cells. Microglia are the brain's immune cells. They play an important role in maintaining the brain's extracellular environment, including clearance of aggregated proteins such as amyloid-beta (A beta). Recent studies suggest that microglia play a more active role in the brain than initially considered. Specifically, microglia provide trophic support to neurons and also regulate synapses. Microglial regulation of neuronal activity may have important consequences for AD. In this article we review the function of microglia in AD and examine the possible relationship between microglial dysfunction and network abnormalities, which occur very early in disease pathogenesis.
引用
收藏
页码:657 / 669
页数:13
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