Komori Takashi, Ishizawa Keisuke, Arai Nobutaka, Hirose Takanori, Mizutani Toshio, Oda Masaya
Department of Clinical Neuropathology, Tokyo Metropolitan Institute for Neuroscience, 2-6 Musashidai, Fuchu City, 183-8526 Tokyo, Japan.
Acta Neuropathol. 2003 Jul;106(1):66-70. doi: 10.1007/s00401-003-0702-5. Epub 2003 Apr 1.
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.
胶质细胞胞质内含物(GCIs)是多系统萎缩(MSA)的组织学标志。在6例MSA患者的尸检大脑中,在GCIs中鉴定出14-3-3蛋白免疫反应性,主要位于基底前脑和小脑的白质组织中。使用双重免疫组织化学,证实了GCIs中14-3-3蛋白和α-突触核蛋白免疫反应性的共定位。GCIs与14-3-3蛋白的免疫标记率在不同区域约为40%至90%。半定量分析显示组织变性程度与14-3-3蛋白免疫反应性GCIs的密度之间存在显著负相关。14-3-3蛋白是通过与靶蛋白中的磷酸化基序结合参与细胞调节的活性辅助因子,而α-突触核蛋白是14-3-3的已知靶点。我们的研究表明,14-3-3蛋白在GCIs中与α-突触核蛋白密切相关,并且14-3-3蛋白可能是GCI形成中α-突触核蛋白的候选辅助因子。