Da Pozzo Eleonora, Giacomelli Chiara, Barresi Elisabetta, Costa Barbara, Taliani Sabrina, Passetti Federico Da Settimo, Martini Claudia
Department of Pharmacy, University of Pisa, Via Bonanno 6, 56126 Pisa, Italy.
Department of Pharmacy, University of Pisa, Via Bonanno 6, 56126 Pisa, Italy
Biochem Soc Trans. 2015 Aug;43(4):559-65. doi: 10.1042/BST20150028. Epub 2015 Aug 3.
The translocator protein (TSPO, 18 kDa), mainly localized in the outer mitochondrial membrane of steroidogenic tissues, is involved in several cellular functions. TSPO level alterations have been reported in a number of human disorders, particularly in cancer, psychiatric and neurological diseases. In the central nervous system (CNS), TSPO is usually expressed in glial cells, but also in some neuronal cell types. Interestingly, the expression of TSPO on glial cells rises after brain injury and increased TSPO expression is often observed in neurological disorders, gliomas, encephalitis and traumatic injury. Since TSPO is up-regulated in brain diseases, several structurally different classes of ligands targeting TSPO have been described as potential diagnostic or therapeutic agents. Recent researches have reported that TSPO ligands might be valuable in the treatment of brain diseases. This review focuses on currently available TSPO ligands, as useful tools for the treatment of neurodegeneration, neuro-inflammation and neurotrauma.
转位蛋白(TSPO,18 kDa)主要定位于类固醇生成组织的线粒体外膜,参与多种细胞功能。已有报道称,TSPO水平改变见于多种人类疾病,尤其是癌症、精神疾病和神经疾病。在中枢神经系统(CNS)中,TSPO通常在胶质细胞中表达,但在某些神经元细胞类型中也有表达。有趣的是,脑损伤后胶质细胞上TSPO的表达会升高,并且在神经疾病、胶质瘤、脑炎和创伤性损伤中经常观察到TSPO表达增加。由于TSPO在脑部疾病中上调,因此已描述了几种结构不同的靶向TSPO的配体类别作为潜在的诊断或治疗药物。最近的研究报道,TSPO配体可能在脑部疾病治疗中具有重要价值。本综述重点关注目前可用的TSPO配体,它们是治疗神经退行性变、神经炎症和神经创伤的有用工具。