Schmidt M L, Gur R E, Gur R C, Trojanowski J Q
Department of Pathology and Laboratory Medicine, University of Pennsylvania School of Medicine, Philadelphia 19104.
Ann Neurol. 1988 Feb;23(2):184-9. doi: 10.1002/ana.410230212.
We examined the possibility that neurofibrillary tangles (NFTs) were heterogeneous in postmortem hippocampus from 22 patients with or without senile dementia of the Alzheimer type. Intraneuronal NFTs and extracellular, or "ghost," NFTs were recognized in situ by only one or the other of two monoclonal antibodies. The first monoclonal antibody, RMO87, stained only intraneuronal NFTs and is specific for phosphate-dependent epitopes in tau and the two high molecular weight neurofilament proteins. The second monoclonal antibody, 2.2B10, is specific for glial fibrillary acidic protein, and it stained only the RMO87-negative extracellular NFTs. Treatment of sections with alkaline phosphatase or sodium dodecyl sulfate, and the isolation of NFTs from hippocampus, did not expose RMO87 binding sites in extracellular NFTs. These observations indicate that neurofilament-like and tau-like epitopes can be lost from NFTs in situ, and that at least two populations of morphologically and immunochemically distinct NFTs exist.
我们研究了22例患有或未患有阿尔茨海默型老年痴呆症患者死后海马体中神经原纤维缠结(NFTs)是否存在异质性的可能性。通过两种单克隆抗体中的一种或另一种在原位识别神经元内NFTs和细胞外或“幽灵”NFTs。第一种单克隆抗体RMO87仅对神经元内NFTs染色,对tau蛋白和两种高分子量神经丝蛋白中的磷酸依赖性表位具有特异性。第二种单克隆抗体2.2B10对胶质纤维酸性蛋白具有特异性,且仅对RMO87阴性的细胞外NFTs染色。用碱性磷酸酶或十二烷基硫酸钠处理切片,以及从海马体中分离NFTs,均未暴露细胞外NFTs中的RMO87结合位点。这些观察结果表明,神经丝样和tau样表位可在原位从NFTs中丢失,且至少存在两种形态和免疫化学上不同的NFTs群体。