Hattori N, Tanaka M, Ozawa T, Mizuno Y
Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
Ann Neurol. 1991 Oct;30(4):563-71. doi: 10.1002/ana.410300409.
We examined the substantia nigra of 8 patients with Parkinson's disease immunohistochemically using antisera against complexes I, II, III, and IV of the mitochondrial electron transport system. In the patients with Parkinson's disease, a fair proportion of the nigral neurons showed reduced staining against the complex I antibody. The proportion of the neurons with reduced staining ranged from 12.7 to 74.1% of the melanized nigral neurons. Although neurons with reduced immunostaining for complex I were also observed in control subjects, the proportion among the nigral neurons was significantly smaller than in parkinsonian patients. Staining for complexes III and IV appeared normal. Staining of substantia nigra for complex II was decreased in 3 parkinsonian patients. These results are consistent with our findings that there is a deletion of gene coding for the four subunits in the mitochondrial DNA located in the striata of parkinsonian patients.
我们使用针对线粒体电子传递系统复合体I、II、III和IV的抗血清,对8例帕金森病患者的黑质进行了免疫组织化学检查。在帕金森病患者中,相当一部分黑质神经元对复合体I抗体的染色减少。染色减少的神经元比例占黑色素化黑质神经元的12.7%至74.1%。虽然在对照受试者中也观察到对复合体I免疫染色减少的神经元,但其在黑质神经元中的比例明显低于帕金森病患者。复合体III和IV的染色看起来正常。3例帕金森病患者黑质对复合体II的染色减少。这些结果与我们的发现一致,即在帕金森病患者的纹状体中,线粒体DNA中编码四个亚基的基因存在缺失。