Yamazaki M, Arai Y, Baba M, Iwatsubo T, Mori O, Katayama Y, Oyanagi K
Department of Neuropathology, Tokyo Metropolitan Institute for Neuroscience, Fuchu, Japan.
J Neuropathol Exp Neurol. 2000 Jul;59(7):585-91. doi: 10.1093/jnen/59.7.585.
We investigated by immunohistochemistry the deposition of alpha-synuclein in the brains of deceased patients with the parkinsonism-dementia complex (PDC) of Guam. Five of 13 PDC brains showed numerous alpha-synuclein positive neuronal inclusions and abnormal neurites, chiefly in the amygdala. Similar alpha-synuclein positive lesions were observed, although to a lesser extent, in the entorhinal cortex and the dorsal vagal nucleus. No alpha-synuclein positive inclusions were observed in motor cortex or locus coeruleus, and only a small number of positive inclusions were found in the Sommer's sector, temporal cortex, or substantia nigra. Some of the alpha-synuclein positive inclusions were reminiscent of cortical Lewy bodies (LB), but many of those in the amygdala coexisted with tau-positive pretangles and/or neurofibrillary tangles (NFT) within the same neurons. In these neurons, tau-positive shells encapsulated alpha-synuclein positive central cores or irregularly shaped alpha-synuclein-positive deposition intermingled with pretangles/NFT. Thus, the present study suggests that a common mechanism may govern aggregation of alpha-synuclein and tau in the amygdala, and that aggregation of alpha-synuclein may play some role in the neurodegenerative process of a tauopathy (i.e. PDC) in which Abeta deposition is virtually absent.
我们通过免疫组织化学方法研究了关岛帕金森病痴呆综合征(PDC)已故患者大脑中α-突触核蛋白的沉积情况。13例PDC患者的大脑中有5例显示出大量α-突触核蛋白阳性神经元包涵体和异常神经突,主要位于杏仁核。在内嗅皮质和迷走神经背核也观察到了类似的α-突触核蛋白阳性病变,不过程度较轻。在运动皮质或蓝斑中未观察到α-突触核蛋白阳性包涵体,在海马 Sommer 区、颞叶皮质或黑质中仅发现少量阳性包涵体。一些α-突触核蛋白阳性包涵体让人联想到皮质路易小体(LB),但杏仁核中的许多阳性包涵体与同一神经元内的tau阳性前缠结和/或神经原纤维缠结(NFT)共存。在这些神经元中,tau阳性外壳包裹着α-突触核蛋白阳性中心核或与前缠结/NFT 交织在一起的不规则形状的α-突触核蛋白阳性沉积物。因此,本研究表明,可能存在一种共同机制控制着杏仁核中α-突触核蛋白和tau的聚集,并且α-突触核蛋白的聚集可能在几乎不存在β-淀粉样蛋白沉积的tau病(即PDC)的神经退行性过程中发挥一定作用。