Department of Neurology, Osaka University Graduate School of Medicine, Osaka, Japan.
Neuropathology. 2022 Apr;42(2):93-103. doi: 10.1111/neup.12812. Epub 2022 Mar 31.
Parkinson's disease (PD) is a neurodegenerative disorder characterized by progressive movement disability accompanied by non-motor symptoms. The neuropathology hallmark of PD is the loss of dopaminergic neurons predominantly in the substantia nigra pars compacta and the presence of intracellular inclusions termed Lewy bodies (LBs), which are mainly composed of α-synuclein (αSyn). Detailed staging based on the distribution and progression pattern of αSyn pathology in the postmortem brains of PD patients revealed correlation with the clinical phenotypes but not invariably. Cumulative evidence from cell and animal studies has implied that αSyn propagation contributes to the anatomical spread of αSyn pathology in the brain. Here, we recount the studies over the past two centuries on the anatomopathological foundations of PD documented. We also review studies on the structural analysis of αSyn and LBs, Braak staging of αSyn pathology, the cell-to-cell propagation of αSyn as well as αSyn fibril polymorphisms, which underlie the phenotypic differences in synucleinopathies.
帕金森病(PD)是一种神经退行性疾病,其特征是进行性运动障碍伴非运动症状。PD 的神经病理学标志是多巴胺能神经元的丧失,主要发生在黑质致密部,并且存在称为路易体(LB)的细胞内包涵体,主要由α-突触核蛋白(αSyn)组成。基于 PD 患者死后大脑中αSyn 病理学分布和进展模式的详细分期与临床表型相关,但并非一成不变。来自细胞和动物研究的累积证据表明,αSyn 的传播有助于αSyn 病理学在大脑中的解剖传播。在这里,我们回顾了过去两个世纪中有关 PD 的解剖病理学基础的研究。我们还回顾了关于 αSyn 和 LB 的结构分析、αSyn 病理学的 Braak 分期、αSyn 的细胞间传播以及αSyn 纤维多态性的研究,这些研究是导致突触核蛋白病表型差异的基础。