Microglial priming in Alzheimer's disease

被引:73
|
作者
Li, Jun-Wei [1 ]
Zong, Yu [2 ]
Cao, Xi-Peng [3 ]
Tan, Lin [2 ]
Tan, Lan [1 ,2 ]
机构
[1] Dalian Med Univ, Qingdao Municipal Hosp, Dept Neurol, Qingdao 266000, Peoples R China
[2] Qingdao Univ, Qingdao Municipal Hosp, Dept Neurol, Qingdao 266071, Peoples R China
[3] Qingdao Univ, Qingdao Municipal Hosp, Clin Res Ctr, Qingdao 266071, Peoples R China
关键词
Alzheimer's disease (AD); amyloid beta (A beta); microglial priming; neuroinflammation; tau-protein; PATTERN-RECOGNITION RECEPTORS; MILD COGNITIVE IMPAIRMENT; SYSTEMIC INFLAMMATION; IMMUNE ACTIVATION; MOUSE MODEL; BRAIN-DEVELOPMENT; OXIDATIVE STRESS; AMYLOID-BETA; WILD-TYPE; NEUROINFLAMMATION;
D O I
10.21037/atm.2018.04.22
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Alzheimer's disease (AD) is a chronic and progressive neurodegenerative disease of central nervous system (CNS). Nowadays, increasing evidence suggests that immune system plays a significant role in the mechanisms of AD's onset and progression. Microglia, the main participator in the immune system of CNS, is always regarded as a protector of our brain in a healthy state and also has a beneficial role in maintaining the homeostasis of CNS microenvironment. However, chronic and sustained stimulation can push microglia into the state termed priming. Primed microglia can induce the production of amyloid beta (A beta), tau pathology, neuroinflammation and reduce the release of neurotrophic factors, resulting in loss of normal neurons in quantity and function that has immense relationship with AD. The therapeutic strategies mainly aimed at modulating the microenvironment and microglial activity in CNS to delay progression and alleviate pathogenesis of AD. Overall, in this review, we highlight the mechanism of microglial priming, and discuss the profound relationship between microglial priming and AD. Besides, we also pay attention to the therapeutic strategies targeting at microglial priming.
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收藏
页数:14
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