Division of Nuclear Medicine and Molecular Imaging, Massachusetts General Hospital, Boston 02114, Massachusetts, United States.
Department of Radiology, Harvard Medical School, 75 Francis Street, Boston 02115, Massachusetts, United States.
J Med Chem. 2021 Dec 23;64(24):17656-17689. doi: 10.1021/acs.jmedchem.1c01571. Epub 2021 Dec 14.
Neuroinflammation is an adaptive response of the central nervous system to diverse potentially injurious stimuli, which is closely associated with neurodegeneration and typically characterized by activation of microglia and astrocytes. As a noninvasive and translational molecular imaging tool, positron emission tomography (PET) could provide a better understanding of neuroinflammation and its role in neurodegenerative diseases. Ligands to translator protein (TSPO), a putative marker of neuroinflammation, have been the most commonly studied in this context, but they suffer from serious limitations. Herein we present a repertoire of different structural chemotypes and novel PET ligand design for classical and emerging neuroinflammatory targets beyond TSPO. We believe that this Perspective will support multidisciplinary collaborations in academic and industrial institutions working on neuroinflammation and facilitate the progress of neuroinflammation PET probe development for clinical use.
神经炎症是中枢神经系统对各种潜在损伤性刺激的适应性反应,与神经退行性变密切相关,其特征通常为小胶质细胞和星形胶质细胞的激活。正电子发射断层扫描(PET)作为一种非侵入性和转化性的分子成像工具,可以更好地了解神经炎症及其在神经退行性疾病中的作用。针对神经炎症的假定标志物——转译启动因子(TSPO)的配体在这方面是研究最多的,但它们存在严重的局限性。在此,我们提出了一系列不同结构的化学型和新型 PET 配体设计,用于 TSPO 以外的经典和新兴神经炎症靶点。我们相信,这一观点将支持在神经炎症领域开展学术和产业机构的多学科合作,并促进神经炎症 PET 探针开发用于临床应用的进展。