Department of Pharmacy, College of Pharmacy, Pusan National University, Busan, 46241, Republic of Korea.
Institute of BioPhysio Sensor Technology, Pusan National University, Busan, 46241, Republic of Korea.
Arch Pharm Res. 2019 May;42(5):416-425. doi: 10.1007/s12272-019-01133-0. Epub 2019 Mar 4.
Glial cells outnumber neurons in the brain and play important roles in the neuroinflammation that accompanies brain damage in neurodegenerative diseases. In Parkinson's disease (PD), dopaminergic neuronal loss is accompanied by inflammatory changes in microglia, astrocytes, innate immune cells, and infiltrating peripheral immune cells. Neuroinflammation is probably a fundamental immune response to protect neurons from harm and compensate for neuronal damage, but at the same time, its neurotoxic effects exacerbate neuron damage. Furthermore, neuroinflammatory response is regulated by immune cells, such as microglia, astrocytes, and peripheral immune cells, and by cytokines and chemokines. Accordingly, it is crucial that we understand how such immune cells in the brain regulate neuroinflammatory responses in PD pathology. This review describes the roles played by glia-mediated neuroinflammation in PD, both good and bad, and the therapeutic strategies used to treat PD.
胶质细胞在大脑中的数量超过神经元,并在神经退行性疾病伴随的脑损伤所引起的神经炎症中发挥重要作用。在帕金森病(PD)中,多巴胺能神经元的丧失伴随着小胶质细胞、星形胶质细胞、固有免疫细胞和浸润的外周免疫细胞的炎症改变。神经炎症可能是一种基本的免疫反应,旨在保护神经元免受伤害并补偿神经元损伤,但同时,其神经毒性作用会加剧神经元损伤。此外,神经炎症反应受到免疫细胞(如小胶质细胞、星形胶质细胞和外周免疫细胞)以及细胞因子和趋化因子的调节。因此,我们必须了解大脑中的这些免疫细胞如何调节 PD 病理中的神经炎症反应。本综述描述了胶质细胞介导的神经炎症在 PD 中的作用,包括好的和坏的方面,以及用于治疗 PD 的治疗策略。