Dupont Anne-Claire, Largeau Bérenger, Santiago Ribeiro Maria Joao, Guilloteau Denis, Tronel Claire, Arlicot Nicolas
CHRU Tours, 2 Boulevard Tonnellé, 37044 Tours, France.
Institut National de la Santé et de la Recherche Médicale U930, 10 Boulevard Tonnellé, 37032 Tours, France.
Int J Mol Sci. 2017 Apr 7;18(4):785. doi: 10.3390/ijms18040785.
In vivo exploration of activated microglia in neurodegenerative diseases is achievable by Positron Emission Tomography (PET) imaging, using dedicated radiopharmaceuticals targeting the translocator protein-18 kDa (TSPO). In this review, we emphasized the major advances made over the last 20 years, thanks to TSPO PET imaging, to define the pathophysiological implication of microglia activation and neuroinflammation in neurodegenerative diseases, including Parkinson's disease, Huntington's disease, dementia, amyotrophic lateral sclerosis, multiple sclerosis, and also in psychiatric disorders. The extent and upregulation of TSPO as a molecular biomarker of activated microglia in the human brain is now widely documented in these pathologies, but its significance, and especially its protective or deleterious action regarding the disease's stage, remains under debate. Thus, we exposed new and plausible suggestions to enhance the contribution of TSPO PET imaging for biomedical research by exploring microglia's role and interactions with other cells in brain parenchyma. Multiplex approaches, associating TSPO PET radiopharmaceuticals with other biomarkers (PET imaging of cellular metabolism, neurotransmission or abnormal protein aggregates, but also other imaging modalities, and peripheral cytokine levels measurement and/or metabolomics analysis) was considered. Finally, the actual clinical impact of TSPO PET imaging as a routine biomarker of neuroinflammation was put into perspective regarding the current development of diagnostic and therapeutic strategies for neurodegenerative diseases.
通过正电子发射断层扫描(PET)成像,使用靶向18 kDa转运蛋白(TSPO)的专用放射性药物,可以在体内探索神经退行性疾病中活化的小胶质细胞。在这篇综述中,我们强调了过去20年来由于TSPO PET成像所取得的主要进展,以确定小胶质细胞活化和神经炎症在神经退行性疾病(包括帕金森病、亨廷顿舞蹈病、痴呆症、肌萎缩侧索硬化症、多发性硬化症)以及精神疾病中的病理生理意义。在这些疾病中,TSPO作为人脑活化小胶质细胞的分子生物标志物的程度和上调情况现在已有广泛记录,但其意义,尤其是其对疾病阶段的保护或有害作用仍存在争议。因此,我们提出了新的、合理的建议,通过探索小胶质细胞在脑实质中的作用及其与其他细胞的相互作用,来增强TSPO PET成像对生物医学研究的贡献。我们考虑了将TSPO PET放射性药物与其他生物标志物相结合的多重方法(细胞代谢、神经传递或异常蛋白质聚集体的PET成像,以及其他成像方式,以及外周细胞因子水平测量和/或代谢组学分析)。最后,鉴于神经退行性疾病诊断和治疗策略的当前发展,探讨了TSPO PET成像作为神经炎症常规生物标志物的实际临床影响。