Shen Zhiwei, Bao Xinjie, Wang Renzhi
Department of Neurosurgery, Peking Union Medical College Hospital, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing, China.
Front Aging Neurosci. 2018 Oct 8;10:314. doi: 10.3389/fnagi.2018.00314. eCollection 2018.
In addition to extracellular β-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 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.
除了细胞外β淀粉样斑块和细胞内神经原纤维缠结外,神经炎症已被确定为阿尔茨海默病(AD)的关键病理特征。一旦被激活,称为小胶质细胞的神经炎症细胞会获得不同的激活表型。在AD的早期,被激活的小胶质细胞主要以神经保护和抗炎的M2表型为主。相反,在AD的后期,小胶质细胞的过度激活被认为是有害的且具有促炎作用,转变为M1表型。针对小胶质细胞调节的治疗策略可能会调节它们的特定表型。幸运的是,随着成像方法的迅速发展,小胶质细胞激活的可视化已经得到了充分探索。在这篇综述中,我们总结了激活的小胶质细胞在AD发病机制中的关键作用以及目前关于AD患者小胶质细胞激活成像的研究。我们探讨了用成像技术识别激活的小胶质细胞表型的可能性,并强调了在AD小鼠中调节小胶质细胞表型的有前景的治疗方法。