Middleton Ryan J, Liu Guo-Jun, Banati Richard B
Life Sciences, Australian Nuclear Science and Technology Organisation, New Illawarra Road, Lucas Heights, NSW 2234, Australia
Life Sciences, Australian Nuclear Science and Technology Organisation, New Illawarra Road, Lucas Heights, NSW 2234, Australia National Imaging Facility, Brain and Mind Research Institute and Faculty of Health Sciences, University of Sydney, 94 Mallett Street, Camperdown, NSW 2050, Australia.
Biochem Soc Trans. 2015 Aug;43(4):553-8. doi: 10.1042/BST20150039. Epub 2015 Aug 3.
The highly conserved 18-kDa translocator protein (TSPO) or peripheral benzodiazepine receptor (PBR), is being investigated as a diagnostic and therapeutic target for disease conditions ranging from inflammation to neurodegeneration and behavioural illnesses. Many functions have been attributed to TSPO/PBR including a role in the mitochondrial permeability transition pore (MPTP), steroidogenesis and energy metabolism. In this review, we detail the recent developments in determining the physiological role of TSPO/PBR, specifically based on data obtained from the recently generated Tspo knockout mouse models. In addition to defining the role of TSPO/PBR, we also describe the value of Tspo knockout mice in determining the selectivity, specificity and presence of any off-target effects of TSPO/PBR ligands.
高度保守的18 kDa转位蛋白(TSPO)或外周苯二氮䓬受体(PBR),正作为从炎症到神经退行性疾病和行为疾病等多种病症的诊断和治疗靶点进行研究。TSPO/PBR具有多种功能,包括在线粒体通透性转换孔(MPTP)、类固醇生成和能量代谢中发挥作用。在本综述中,我们详细介绍了确定TSPO/PBR生理作用方面的最新进展,特别是基于最近构建的Tspo基因敲除小鼠模型所获得的数据。除了明确TSPO/PBR的作用外,我们还描述了Tspo基因敲除小鼠在确定TSPO/PBR配体的选择性、特异性以及任何脱靶效应方面的价值。