Abstract

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 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.

Highlights

  • Alzheimer’s disease (AD), the most common cause of dementia, was first described by Dr Alois Alzheimer in 1907 (Vishal et al, 2011)

  • We mainly aim to review the possibility of imaging microglial activation in AD patients using magnetic resonance imaging (MRI) and Positron emission tomography (PET), which have the potential for further in vivo application in human beings

  • Microglial activation plays a significant role in the underlying pathology of AD

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Summary

INTRODUCTION

Alzheimer’s disease (AD), the most common cause of dementia, was first described by Dr Alois Alzheimer in 1907 (Vishal et al, 2011). It has been realized that a simple M1 or M2 phenotype may not capture the whole status of activated microglia (Ransohoff, 2016b; Tang and Le, 2016; Plescher et al, 2018), this classification serves as a crucial guide for microglia-targeted treatment in AD patients. Thanks to the rapid development of imaging technologies, imaging microglial activation in vivo is already possible This kind of technology is unable to discriminate the exact phenotype of activated microglia, we can distinguish the phenotype according to the disease stage. This technique might be applied to direct the treatment of AD patients in the hospital. We summarize the critical role of microglial activation in the pathogenesis of AD, review the published studies on imaging of microglial activation, and highlight a novel therapeutic approach that exerts neuroprotective effects by modulating microglial activation states in AD patients

PATHOLOGICAL SIGNIFICANCE OF MICROGLIAL PHENOTYPES IN AD
THE THERAPEUTIC EFFECTS OF DRUGS THAT ACT ON MICROGLIA IN AD
CURRENT IMAGING OF MICROGLIA IN VIVO IN AD PATIENTS
Increase in both MCI and AD
CONCLUSION
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