Clinical PET Imaging of Microglial Activation: Implications for Microglial Therapeutics in Alzheimer's Disease

被引:60
作者
Shen, Zhiwei [1 ]
Bao, Xinjie [1 ]
Wang, Renzhi [1 ]
机构
[1] Chinese Acad Med Sci, Dept Neurosurg, Peking Union Med Coll Hosp, Peking Union Med Coll, Beijing, Peoples R China
基金
中国国家自然科学基金; 国家高技术研究发展计划(863计划); 北京市自然科学基金;
关键词
microglia; therapy; Alzheimer's disease; imaging; phenotype; MILD COGNITIVE IMPAIRMENT; TRANSLOCATOR PROTEIN TSPO; STEM-CELL THERAPY; AMYLOID-BETA; MOUSE MODEL; 18; KDA; ALTERNATIVE ACTIVATION; MEMORY IMPAIRMENT; M1/M2; PHENOTYPE; INNATE IMMUNITY;
D O I
10.3389/fnagi.2018.00314
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
In addition to extracellular beta-amyloid plaques and intracellular neurofibrillary tangles, neuroinflammation has been identified as a key pathological characteristic of Alzheimer's disease (AD). Once activated, neuroinflammatory cells called microglia acquire different activation phenotypes. At the early stage of AD, activated microglia are mainly dominated by the neuroprotective and anti-inflammatory M2 phenotype. Conversely, in the later stage of AD, the excessive activation of microglia is considered detrimental and pro-inflammatory, turning into the M1 phenotype. Therapeutic strategies targeting the modulation of microglia may regulate their specific phenotype. Fortunately, with the rapid development of in vivo imaging methodologies, visualization of microglial activation has been well-explored. In this review, we summarize the critical role of activated microglia during the pathogenesis of AD and current studies concerning imaging of microglial activation in AD patients. We explore the possibilities for identifying activated microglial phenotypes with imaging techniques and highlight promising therapies that regulate the microglial phenotype in AD mice.
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页数:10
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