Department of Neurobiology, George S. Wise Faculty of Life Sciences, Tel Aviv University, Sherman building, Room 424, 69978, Tel Aviv, Israel.
Sagol School of Neuroscience, George S. Wise Faculty of Life Sciences, Tel Aviv University, Tel Aviv, Israel.
J Neural Transm (Vienna). 2020 Feb;127(2):149-158. doi: 10.1007/s00702-020-02154-6. Epub 2020 Feb 3.
Parkinson's disease (PD) is a neurodegenerative disease associated with motor deficiency and rigidity. The genetic risks of the disease is reported to be between 5 and 10% depending on the background of the population. While PD is not considered an immune-mediated disease, amounting evidence in recent years suggests a major role of inflammation in the progression of PD. Markers of inflammation can be found around the regions of risk and adjacent to the appearance of Lewy bodies within the basal ganglia and the substantia nigra (SN) that are associated with PD pathology. Microglia, an important type of brain cell, has been reported to play a major role in mediating neuroinflammation and in PD disease pathology. This review aims to point out the potential role of microglia in disease progression and suggest that the interaction of microglia with the dopaminergic neurons may also facilitate the specificity of the disease in brain regions affected by PD.
帕金森病(PD)是一种与运动缺陷和僵硬相关的神经退行性疾病。据报道,该疾病的遗传风险在 5%至 10%之间,具体取决于人群背景。虽然 PD 不被认为是一种免疫介导的疾病,但近年来越来越多的证据表明炎症在 PD 的进展中起着重要作用。在与 PD 病理相关的基底神经节和黑质(SN)的风险区域及其周围,以及Lewy 体出现的部位,都可以发现炎症标志物。已报道小胶质细胞(一种重要的脑细胞类型)在介导神经炎症和 PD 疾病病理中起着主要作用。本综述旨在指出小胶质细胞在疾病进展中的潜在作用,并表明小胶质细胞与多巴胺能神经元的相互作用也可能促进 PD 影响的大脑区域中疾病的特异性。