Gambetti P, Shecket G, Ghetti B, Hirano A, Dahl D
J Neuropathol Exp Neurol. 1983 Jan;42(1):69-79. doi: 10.1097/00005072-198301000-00006.
Brain samples from cases of Alzheimer's disease, postencephalitic Parkinson's disease, progressive supranuclear palsy, amyotrophic lateral sclerosis, and Pick's disease, as well as from a case of Alzheimer's disease with a large number of Hirano bodies, were stained with the peroxidase-anti-peroxidase method using an antiserum previously shown to immunoreact with normal neurofilaments and neurofilament polypeptides. The specificity of this serum was confirmed by absorption an purified neurofilament proteins. Neurofibrillary tangles of Alzheimer's disease, postencephalitic Parkinson's disease, and progressive supranuclear palsy, Pick's bodies, and the fibrillary inclusions of amyotrophic lateral sclerosis were all immunostained. Hirano bodies showed no immunostaining. Thus, with the exception of the Hirano bodies, all the neuronal fibrillary inclusions examined appeared to share common antigenic characteristics. The orgin of all these structures from normal neurofilaments is postulated.
取自阿尔茨海默病、脑炎后帕金森病、进行性核上性麻痹、肌萎缩侧索硬化症和皮克病病例的脑样本,以及取自一例有大量 Hirano 小体的阿尔茨海默病病例的脑样本,使用先前已证明能与正常神经丝和神经丝多肽发生免疫反应的抗血清,通过过氧化物酶 - 抗过氧化物酶方法进行染色。该血清的特异性通过与纯化的神经丝蛋白吸附得以证实。阿尔茨海默病、脑炎后帕金森病和进行性核上性麻痹的神经原纤维缠结、皮克小体以及肌萎缩侧索硬化症的纤维状包涵体均被免疫染色。Hirano 小体未显示免疫染色。因此,除 Hirano 小体外,所有检查的神经元纤维状包涵体似乎都具有共同的抗原特征。推测所有这些结构均起源于正常神经丝。