Yao Rumeng, Pan Ruiyuan, Shang Chao, Li Xiaoheng, Cheng Jinbo, Xu Jiangping, Li Yunfeng
Department of Neuropharmacology and Drug Discovery, School of Pharmaceutical Sciences, Southern Medical University, Guangzhou, China.
State Key Laboratory of Toxicology and Medical Countermeasures, Beijing Key Laboratory of Neuropsychopharmacology, Beijing Institute of Pharmacology and Toxicology, Beijing, China.
Front Pharmacol. 2020 Jun 30;11:986. doi: 10.3389/fphar.2020.00986. eCollection 2020.
TSPO is mainly expressed in the mitochondrial outer membrane of microglia in the central nervous system, and its expression is greatly increased when microglia are activated. However, the role and mechanism of this protein in microglial activation is not well characterized. In this study, we investigated the role of TSPO in microglial activation by isolating primary microglia from knockout mice and constructing TSPO-knockdown microglial cell line. We found that TSPO deficiency significantly inhibited microglial activation induced by LPS or IL-4. Mechanistically, TSPO deficiency greatly decreased the mitochondrial membrane potential and ATP production. Moreover, an analysis of cellular energy metabolism showed that TSPO deficiency suppressed mitochondrial oxidative phosphorylation (OXPHOS) and glycolysis, resulting in microglial overall metabolic deficits. Together, our results reveal a crucial role of TSPO in microglial activation through the regulation of mitochondrial metabolism, thus providing a potential therapeutic target for neuroinflammation-related diseases of the central nervous system.
TSPO主要表达于中枢神经系统小胶质细胞的线粒体外膜,当小胶质细胞被激活时其表达会大幅增加。然而,这种蛋白质在小胶质细胞激活中的作用和机制尚未得到充分阐明。在本研究中,我们通过从基因敲除小鼠中分离原代小胶质细胞并构建TSPO敲低的小胶质细胞系,研究了TSPO在小胶质细胞激活中的作用。我们发现TSPO缺陷显著抑制了由脂多糖(LPS)或白细胞介素-4(IL-4)诱导的小胶质细胞激活。从机制上讲,TSPO缺陷极大地降低了线粒体膜电位和ATP生成。此外,细胞能量代谢分析表明,TSPO缺陷抑制了线粒体氧化磷酸化(OXPHOS)和糖酵解,导致小胶质细胞整体代谢缺陷。总之,我们的结果揭示了TSPO通过调节线粒体代谢在小胶质细胞激活中的关键作用,从而为中枢神经系统神经炎症相关疾病提供了一个潜在的治疗靶点。