Wakabayashi K, Matsumoto K, Takayama K, Yoshimoto M, Takahashi H
Brain Disease Research Center, Niigata University, Japan.
Neurosci Lett. 1997 Dec 12;239(1):45-8. doi: 10.1016/s0304-3940(97)00891-4.
NACP, originally identified as a precursor of the non-Abeta component of Alzheimer's disease amyloid (NAC), is now known to be identical to alpha-synuclein, a presynaptic protein in the human brain. Recently, a mutation in the alpha-synuclein gene in families with autosomal dominant Parkinson's disease (PD) was identified. We carried out immunohistochemical examinations of the brains of sporadic PD patients using anti-NACP and anti-ubiquitin antibodies. Consistent with previous studies, the anti-NACP antibody immunostained the neuropil in a punctate pattern throughout the brain. Moreover, much stronger NACP immunoreactivity was found in Lewy bodies and degenerating neurites in the brainstem. Serial sections immunolabeled with anti-ubiquitin or anti-NACP showed that all ubiquitin-immunoreactive LBs were also NACP-immunoreactive. These findings suggest that alteration of NACP metabolism is involved in the pathogenesis of PD, particularly in Lewy body formation, leading to neurodegeneration.
NACP最初被鉴定为阿尔茨海默病淀粉样蛋白(NAC)非Aβ成分的前体,现在已知它与α-突触核蛋白相同,α-突触核蛋白是人类大脑中的一种突触前蛋白。最近,在常染色体显性帕金森病(PD)家族中发现了α-突触核蛋白基因的突变。我们使用抗NACP和抗泛素抗体对散发性PD患者的大脑进行了免疫组织化学检查。与先前的研究一致,抗NACP抗体以点状模式对全脑的神经纤维网进行免疫染色。此外,在脑干的路易小体和变性神经突中发现了更强的NACP免疫反应性。用抗泛素或抗NACP免疫标记的连续切片显示,所有泛素免疫反应性路易小体也具有NACP免疫反应性。这些发现表明,NACP代谢的改变参与了PD的发病机制,特别是在路易小体形成过程中,导致神经退行性变。