Wakabayashi K, Hayashi S, Yoshimoto M, Kudo H, Takahashi H
Brain Disease Research Center, Brain Research Institute, Niigata University, Japan.
Acta Neuropathol. 2000 Jan;99(1):14-20. doi: 10.1007/pl00007400.
The precursor of the non-Abeta component of Alzheimer's disease amyloid (NACP), also called alpha-synuclein, is a major component of Lewy bodies in Parkinson's disease (PD) as well as of neuronal and oligodendroglial cytoplasmic inclusions in multiple system atrophy. We previously reported argyrophilic, tau-negative glial inclusions in the midbrains of patients with PD and have now conducted immunocytochemical and ultrastructural examinations. The PD glial inclusions also are immunoreactive for NACP/alpha-synuclein, but not for beta-synuclein, and ultrastructurally are composed of filamentous structures about 25-40 nm in diameter. Double immunolabeling showed that the inclusions were present in both astrocytic and oligodendroglial cells. They were located within the substantia nigra in 13 of 30 patients with PD and outside the nigra in 24. The number of inclusions was correlated with the severity of nigral neuronal loss. These findings indicate that abnormal accumulation of NACP/alpha-synuclein in glial cells is a pathological feature of PD related to its progression.
阿尔茨海默病淀粉样蛋白非Aβ成分(NACP)的前体,也称为α-突触核蛋白,是帕金森病(PD)中路易小体的主要成分,也是多系统萎缩中神经元和少突胶质细胞质内包涵体的主要成分。我们之前报道了PD患者中脑内嗜银性、tau蛋白阴性的胶质细胞内包涵体,现在进行了免疫细胞化学和超微结构检查。PD胶质细胞内包涵体对NACP/α-突触核蛋白也有免疫反应,但对β-突触核蛋白无反应,超微结构上由直径约25 - 40nm的丝状结构组成。双重免疫标记显示这些包涵体存在于星形胶质细胞和少突胶质细胞中。在30例PD患者中,13例的包涵体位于黑质内,24例位于黑质外。包涵体数量与黑质神经元丢失的严重程度相关。这些发现表明胶质细胞中NACP/α-突触核蛋白的异常积累是与PD进展相关的病理特征。