路易氏体型失智症
路易体
病理
神经退行性变
α-突触核蛋白
帕金森病
共核细胞病
神经丝
神经科学
突触核蛋白
疾病
医学
生物
痴呆
免疫组织化学
作者
Maria Grazia Spillantini,Marie L. Schmidt,Virginia M.‐Y. Lee,John Q. Trojanowski,Ross Jakes,Michel Goedert
出处
期刊:Nature
[Nature Portfolio]
日期:1997-08-28
卷期号:388 (6645): 839-840
被引量:7671
摘要
Lewy bodies, a defining pathological characteristic of Parkinson's disease and dementia with Lewy bodies (DLB)1,2,3,4, constitute the second most common nerve cell pathology, after the neurofibrillary lesions of Alzheimer's disease. Their formation may cause neurodegeneration, but their biochemical composition is unknown. Neurofilaments and ubiquitin are present5,6,7,8, but it is unclear whether they are major components of the filamentous material of the Lewy body9,10. Here we describe strong staining of Lewy bodies from idiopathic Parkinson's disease with antibodies for α-synuclein, a presynaptic protein of unknown function which is mutated in some familial cases of the disease11. α-Synuclein may be the main component of the Lewy body in Parkinson's disease. We also show staining for α-synuclein of Lewy bodies from DLB, indicating that the Lewy bodies from these two diseases may have identical compositions.
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