Cheng Ying-Ying, Chen Bei-Yu, Bian Gan-Lan, Ding Yin-Xiu, Chen Liang-Wei
Department of Anatomy, Histology and Embryology, The Key Laboratory of Cerebrocranial Diseases, Ningxia Medical University, Yinchuan, 750004, People's Republic of China.
Department of Orthopedics, Xijing Hospital, The Fourth Military Medical University, Xi'an, 710032, People's Republic of China.
Mol Neurobiol. 2022 Apr;59(4):2642-2655. doi: 10.1007/s12035-022-02758-x. Epub 2022 Feb 10.
Abundant reactive gliosis and neuroinflammation are typical pathogenetic hallmarks of brains in Parkinson's disease (PD) patients, but regulation mechanisms are poorly understood. We are interested in role of programmed death-1 (PD-1) in glial reaction, neuroinflammation and neuronal injury in PD pathogenesis. Using PD mouse model and PD-1 knockout (KO) mice, we designed wild-type-control (WT-CON), WT-1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (WT-MPTP), PD-1-KO-control (KO-CON) and PD-1-KO-MPTP (KO-MPTP), and observed motor dysfunction of animal, morphological distribution of PD-1-positive cells, dopaminergic neuronal injury, glial activation and generation of inflammatory cytokines in midbrains by motor behavior detection, immunohistochemistry and western blot. WT-MPTP mouse model exhibited decrease of PD-1/Iba1-positive microglial cells in the substantia nigra compared with WT-CON mice. By comparison of four groups, PD-1 deficiency showed exacerbation in motor dysfunction of animals, decreased expression of TH protein and TH-positive neuronal protrusions. PD-1 deficiency enhanced microglial activation, production of proinflammatory cytokines like inducible nitric oxide synthase, tumor necrosis factor-α, interleukin-1β and interleukin-6, and expression and phosphorylation of AKT and ERK1/2 in the substantia nigra of MPTP model. We concluded that PD-1 deficiency could aggravate motor dysfunction of MPTP mouse model by inducing microglial activation and neuroinflammation in midbrains, suggesting that PD-1 signaling abnormality might be possibly involved in PD pathogenesis.
丰富的反应性胶质增生和神经炎症是帕金森病(PD)患者大脑典型的致病特征,但调控机制尚不清楚。我们对程序性死亡-1(PD-1)在PD发病机制中的胶质反应、神经炎症和神经元损伤中的作用感兴趣。利用PD小鼠模型和PD-1基因敲除(KO)小鼠,我们设计了野生型对照(WT-CON)、野生型1-甲基-4-苯基-1,2,3,6-四氢吡啶(WT-MPTP)、PD-1-KO对照(KO-CON)和PD-1-KO-MPTP(KO-MPTP)组,并通过运动行为检测、免疫组织化学和蛋白质印迹观察动物的运动功能障碍、PD-1阳性细胞的形态分布、多巴胺能神经元损伤、胶质细胞活化以及中脑炎性细胞因子的产生。与WT-CON小鼠相比,WT-MPTP小鼠模型黑质中PD-1/Iba1阳性小胶质细胞减少。通过四组比较,PD-1缺乏导致动物运动功能障碍加重,TH蛋白表达和TH阳性神经元突起减少。PD-1缺乏增强了MPTP模型小鼠黑质中小胶质细胞的活化、促炎细胞因子如诱导型一氧化氮合酶、肿瘤坏死因子-α、白细胞介素-1β和白细胞介素-6的产生,以及AKT和ERK1/2的表达和磷酸化。我们得出结论,PD-1缺乏可通过诱导中脑小胶质细胞活化和神经炎症加重MPTP小鼠模型的运动功能障碍,提示PD-1信号异常可能参与PD的发病机制。