Department of Nephrology, Yangpu Hospital, School of Medicine, Tongji University, Shanghai, China.
Department of Radiopharmacy and Molecular Imaging, School of Pharmacy, Fudan University, Shanghai, China.
Front Immunol. 2021 Sep 16;12:739130. doi: 10.3389/fimmu.2021.739130. eCollection 2021.
Neuroinflammation play an important role in Alzheimer's disease pathogenesis. Advances in molecular imaging using positron emission tomography have provided insights into the time course of neuroinflammation and its relation with Alzheimer's disease central pathologies in patients and in animal disease models. Recent single-cell sequencing and transcriptomics indicate dynamic disease-associated microglia and astrocyte profiles in Alzheimer's disease. Mitochondrial 18-kDa translocator protein is the most widely investigated target for neuroinflammation imaging. New generation of translocator protein tracers with improved performance have been developed and evaluated along with tau and amyloid imaging for assessing the disease progression in Alzheimer's disease continuum. Given that translocator protein is not exclusively expressed in glia, alternative targets are under rapid development, such as monoamine oxidase B, matrix metalloproteinases, colony-stimulating factor 1 receptor, imidazoline-2 binding sites, cyclooxygenase, cannabinoid-2 receptor, purinergic P2X7 receptor, P2Y12 receptor, the fractalkine receptor, triggering receptor expressed on myeloid cells 2, and receptor for advanced glycation end products. Promising targets should demonstrate a higher specificity for cellular locations with exclusive expression in microglia or astrocyte and activation status (pro- or anti-inflammatory) with highly specific ligand to enable brain imaging. In this review, we summarised recent advances in the development of neuroinflammation imaging tracers and provided an outlook for promising targets in the future.
神经炎症在阿尔茨海默病发病机制中起重要作用。正电子发射断层扫描(PET)分子成像技术的进步为我们深入了解神经炎症的时间进程及其与患者和动物疾病模型中阿尔茨海默病核心病理的关系提供了帮助。最近的单细胞测序和转录组学研究表明,阿尔茨海默病中存在动态的与疾病相关的小胶质细胞和星形胶质细胞特征。线粒体 18kDa 转位蛋白(TSPO)是研究最广泛的神经炎症成像靶点。具有更好性能的新一代 TSPO 示踪剂已经被开发和评估,同时也对 tau 和淀粉样蛋白进行成像,以评估阿尔茨海默病连续体中的疾病进展。鉴于 TSPO 并非仅在神经胶质细胞中表达,替代靶点正在迅速开发中,例如单胺氧化酶 B、基质金属蛋白酶、集落刺激因子 1 受体、咪唑啉 2 结合位点、环氧化酶、大麻素 2 受体、嘌呤能 P2X7 受体、P2Y12 受体、 fractalkine 受体、髓样细胞触发受体 2 和晚期糖基化终产物受体。有前途的靶点应该表现出更高的特异性,能够在小胶质细胞或星形胶质细胞中具有独特表达的细胞位置上,并能够在细胞激活状态(促炎或抗炎)下特异性结合配体,从而实现对大脑的成像。在这篇综述中,我们总结了神经炎症成像示踪剂的最新进展,并对未来有前途的靶点进行了展望。