Alam Md Maqusood, Lee Jihye, Lee Sang-Yoon
Neuroscience Research Institute, Gachon University, Incheon, 20565 South Korea.
Department of Neuroscience, College of Medicine, Gachon University, Incheon, 21936 South Korea.
Nucl Med Mol Imaging. 2017 Dec;51(4):283-296. doi: 10.1007/s13139-017-0475-8. Epub 2017 Mar 16.
Neuroinflammation is heavily associated with various neurological diseases including Alzheimer's disease, Parkinson's disease, multiple sclerosis, and stroke. It is strongly characterized by the activation of microglia which can be visualized using position emission tomography (PET). Traditionally, translocator protein 18 kDa (TSPO) has been the preferred target for imaging the inflammatory progression of the microglial component. TSPO is expressed in the outer mitochondrial membrane and present in very low concentrations in the healthy human brain, but is markedly upregulated in response to brain injury and inflammation. Due to its value as a marker of microglial activation and subsequent utility for evaluating neuroinflammation in CNS disorders, several classes of TSPO radioligands have been developed and evaluated. However, the application of these second-generation TSPO radiotracers has been subject to several limiting factors, including a polymorphism that affects TSPO binding. This review focuses on recent developments in TSPO imaging, as well as current limitations and suggestions for future directions from a medical imaging perspective.
神经炎症与包括阿尔茨海默病、帕金森病、多发性硬化症和中风在内的多种神经系统疾病密切相关。其显著特征是小胶质细胞的激活,这可以通过正电子发射断层扫描(PET)进行可视化。传统上,18 kDa转位蛋白(TSPO)一直是成像小胶质细胞成分炎症进展的首选靶点。TSPO在外线粒体膜中表达,在健康人脑中浓度极低,但在脑损伤和炎症反应中会显著上调。由于其作为小胶质细胞激活标志物的价值以及随后在评估中枢神经系统疾病中的神经炎症方面的效用,已开发并评估了几类TSPO放射性配体。然而,这些第二代TSPO放射性示踪剂的应用受到几个限制因素的影响,包括影响TSPO结合的多态性。本综述重点关注TSPO成像的最新进展,以及从医学成像角度看当前的局限性和未来方向的建议。