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α-synuclein immunoreactivity in glial cytoplasmic inclusions in multiple system atrophy
被引:523
作者:
Wakabayashi, K
Yoshimoto, M
Tsuji, S
Takahashi, H
机构:
[1] Niigata Univ, Brain Res Inst, Brain Dis Res Ctr, Niigata 9518585, Japan
[2] Taisho Pharmaceut Co Ltd, Med Res Labs, Mol Biol Lab, Ohmiya, Saitama 3300031, Japan
[3] Niigata Univ, Brain Res Inst, Dept Neurol, Niigata 9518585, Japan
[4] Niigata Univ, Brain Res Inst, Dept Pathol, Niigata 9518585, Japan
关键词:
alpha-synuclein;
multiple system atrophy;
glial cytoplasmic inclusion;
oligodendrocyte;
tubulin;
neurodegeneration;
immunohistochemistry;
D O I:
10.1016/S0304-3940(98)00407-8
中图分类号:
Q189 [神经科学];
学科分类号:
071006 ;
摘要:
Lewy bodies in Parkinson's disease (PD) are strongly immunoreactive with antibodies against alpha-synuclein, which is mutated in some familial cases of the disease. We carried out immunohistochemical examinations of the brains of multiple system atrophy (MSA) patients using anti-alpha-synuclein antibodies. Strong a-synuclein immunoreactivity was found in glial cytoplasmic inclusions (GCIs), which are of oligodendroglial origin and occur exclusively in MSA. alpha-Synuclein-immunoreactive neuronal cytoplasmic inclusions (NCIs) were also found occasionally in the substantia nigra, pontine and inferior olivary nuclei, and dentate fascia. These findings indicate that alpha-synuclein is also a major component of GCIs and NCIs in MSA and strongly suggest that alpha-synuclein aggregation is a common process in certain neurodegenerative diseases, including PD and MSA. (C) 1998 Published by Elsevier Science Ireland Ltd. All rights reserved.
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页码:180 / 182
页数:3
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