期刊论文详细信息
Structures of alpha-synuclein filaments from human brains with Lewy pathology
Article
关键词: MULTIPLE SYSTEM ATROPHY;    PARKINSONS-DISEASE;    DEMENTIA;    BODIES;    MUTATION;    PHOSPHORYLATION;    AGGREGATION;    INCLUSIONS;    COMPONENT;    TAU;   
DOI  :  10.1038/s41586-022-05319-3
来源: SCIE
【 摘 要 】
Parkinson's disease (PD) is the most common movement disorder, with resting tremor, rigidity, bradykinesia and postural instability being major symptoms(1). Neuropathologically, it is characterized by the presence of abundant filamentous inclusions of alpha-synuclein in the form of Lewy bodies and Lewy neurites in some brain cells, including dopaminergic nerve cells of the substantia nigra(2). PD is increasingly recognised as a multisystem disorder, with cognitive decline being one of its most common non-motor symptoms. Many patients with PD develop dementia more than 10 years after diagnosis(3). PD dementia (PDD) is clinically and neuropathologically similar to dementia with Lewy bodies (DLB), which is diagnosed when cognitive impairment precedes parkinsonian motor signs or begins within one year from their onset(4). In PDD, cognitive impairment develops in the setting of well-established PD. Besides PD and DLB, multiple system atrophy (MSA) is the third major synucleinopathy(5). It is characterized by the presence of abundant filamentous alpha-synuclein inclusions in brain cells, especially oligodendrocytes (Papp-Lantos bodies). We previously reported the electron cryo-microscopy structures of two types of alpha-synuclein filament extracted from the brains of individuals with MSA(6). Each filament type is made of two different protofilaments. Here we report that the cryo-electron microscopy structures of alpha-synuclein filaments from the brains of individuals with PD, PDD and DLB are made of a single protofilament (Lewy fold) that is markedly different from the protofilaments of MSA. These findings establish the existence of distinct molecular conformers of assembled alpha-synuclein in neurodegenerative disease.
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