Wakabayashi K, Yoshimoto M, Fukushima T, Koide R, Horikawa Y, Morita T, Takahashi H
Brain Disease Research Center, Brain Research Institute, Niigata University, Japan.
Neuropathol Appl Neurobiol. 1999 Oct;25(5):363-8. doi: 10.1046/j.1365-2990.1999.00193.x.
Alpha-Synuclein (originally called precursor of the non-Abeta component of Alzheimer's disease amyloid-NACP) is a presynaptic nerve terminal protein and is now known to be a major component of Lewy bodies (LBs) in Parkinson's disease. Previous studies have shown that LBs are occasionally found in patients with Hallervorden-Spatz disease (HSD), a hereditary or sporadic neuroaxonal dystrophy. Therefore, an immunocytochemical examination of the brain tissues from two patients with HSD for alpha-synuclein/NACP was performed. In both cases, LBs were observed in the substantia nigra, locus ceruleus and other subcortical nuclei. These LBs were strongly immunolabelled with anti-alpha-synuclein/NACP. Moreover, abnormal alpha-synuclein/NACP-immunoreactive structures in the neuronal somata and processes were found in the cerebral neocortex, hippocampus, basal ganglia, thalamus, pontine and inferior olivary nuclei, spinal grey matter, and peripheral sympathetic ganglia. Although numerous dystrophic axons (spheroids) were found throughout the brain, either none or only a few were positive for alpha-synuclein/NACP. These findings suggest that widespread accumulation of alpha-synuclein/NACP is a pathological feature in patients suffering from HSD with LBs, and that this phenomenon is unrelated to axonal spheroid formation.
α-突触核蛋白(最初称为阿尔茨海默病淀粉样蛋白非Aβ成分的前体-NACP)是一种突触前神经末梢蛋白,现在已知是帕金森病路易小体(LBs)的主要成分。先前的研究表明,在遗传性或散发性神经轴突营养不良的Hallervorden-Spatz病(HSD)患者中偶尔会发现路易小体。因此,对两名HSD患者的脑组织进行了α-突触核蛋白/NACP的免疫细胞化学检查。在这两个病例中,在黑质、蓝斑和其他皮质下核中均观察到路易小体。这些路易小体被抗α-突触核蛋白/NACP强烈免疫标记。此外,在大脑新皮质、海马、基底神经节、丘脑、脑桥和下橄榄核、脊髓灰质以及外周交感神经节的神经元胞体和突起中发现了异常的α-突触核蛋白/NACP免疫反应性结构。尽管在整个大脑中发现了大量营养不良性轴突(球体),但其中没有或只有少数对α-突触核蛋白/NACP呈阳性。这些发现表明,α-突触核蛋白/NACP的广泛积累是患有伴有路易小体的HSD患者的病理特征,并且这种现象与轴突球体形成无关。