Immunoexpression of 14-3-3 proteins in glial cytoplasmic inclusions of multiple system atrophy

被引:22
作者
Komori, T
Ishizawa, K
Arai, N
Hirose, T
Mizutani, T
Oda, M
机构
[1] Tokyo Metropolitan Inst Neurosci, Dept Clin Neuropathol, Fuchu, Tokyo 1838526, Japan
[2] Tokyo Metropolitan Neurol Hosp, Dept Pathol, Tokyo, Japan
[3] Saitama Med Sch, Dept Pathol, Moroyama, Saitama, Japan
关键词
14-3-3; proteins; glial cytoplasmic inclusions; multiple system atrophy; alpha-synuclein; immunohistochemistry;
D O I
10.1007/s00401-003-0702-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Glial cytoplasmic inclusions (GCIs) are the histological hallmark of multiple system atrophy (MSA). In six postmortem brains of patients with MSA, 14-3-3-protein immunoreactivity was identified in GCIs predominately in the white matter tissue of the basal forebrain and cerebellum. Using double immunohistochemistry, co-localization of 14-3-3-protein and alpha-synuclein immunoreactivities in the GCIs was confirmed. The immunolabeling rate of GCIs with 14-3-3 proteins varied regionally from approximately 40% to 90%. Semiquantitative analysis yielded a significant negative correlation between degree of tissue degeneration and density of 14-3-3-protein-immunoreactive GCIs. The 14-3-3 proteins are active cofactors involved in cellular regulation through binding to phosphorylated motifs in target proteins and alpha-synuclein is a known target of 14-3-3: Our study suggests that 14-3-3 proteins are closely associated with alpha-synuclein in GCIs and 14-3-3 proteins may be candidate cofactors of alpha-synuclein in GCI formation.
引用
收藏
页码:66 / 70
页数:5
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