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α-突触核蛋白病:帕金森病、路易体痴呆和多系统萎缩。

The alpha-synucleinopathies: Parkinson's disease, dementia with Lewy bodies, and multiple system atrophy.

作者信息

Spillantini M G, Goedert M

机构信息

Department of Neurology and Brain Repair Centre, University of Cambridge, Cambridge, UK.

出版信息

Ann N Y Acad Sci. 2000;920:16-27. doi: 10.1111/j.1749-6632.2000.tb06900.x.

Abstract

Parkinson's disease is the second most common neurodegenerative disease, after Alzheimer's disease. Neuropathologically, it is characterized by the degeneration of populations of nerve cells that develop filamentous inclusions in the form of Lewy bodies and Lewy neurites. Recent work has shown that the filamentous inclusions of Parkinson's disease are made of the protein alpha-synuclein and that rare, familial forms of Parkinson's disease are caused by missense mutations in the alpha-synuclein gene. Besides Parkinson's disease, the filamentous inclusions of two additional neurodegenerative diseases, namely, dementia with Lewy bodies and multiple system atrophy, have also been found to be made of alpha-synuclein. Recombinant alpha-synuclein has been shown to assemble into filaments with similar morphologies to those found in the human diseases and with a cross-beta fiber diffraction pattern. The new work has established the alpha-synucleinopathies as a major class of neurodegenerative disease.

摘要

帕金森病是仅次于阿尔茨海默病的第二常见神经退行性疾病。在神经病理学上,其特征是神经细胞群体发生退化,形成路易小体和路易神经突形式的丝状内含物。最近的研究表明,帕金森病的丝状内含物由α-突触核蛋白构成,而且罕见的家族性帕金森病形式是由α-突触核蛋白基因的错义突变引起的。除帕金森病外,另外两种神经退行性疾病,即路易体痴呆和多系统萎缩的丝状内含物也已被发现由α-突触核蛋白构成。重组α-突触核蛋白已被证明能组装成形态与人疾病中发现的相似且具有交叉β纤维衍射图谱的细丝。这项新研究已将α-突触核蛋白病确立为一类主要的神经退行性疾病。

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