Miller D W, Johnson J M, Solano S M, Hollingsworth Z R, Standaert D G, Young A B
Cell Biology and Gene Expression Section, Laboratory of Neurogenetics, NIA, Bethesda, MD 20892-3707, USA.
J Neural Transm (Vienna). 2005 Dec;112(12):1613-24. doi: 10.1007/s00702-005-0378-1.
alpha-Synuclein is a major constituent of glial cytoplasmic inclusions (GCIs), which are pathognomic for multiple system atrophy (MSA). We have previously demonstrated that in normal human brain, alpha-synuclein mRNA has a restricted pattern of neuronal expression and no apparent glial expression. The current study used double-label in situ hybridization to determine if alpha-synuclein mRNA is expressed by oligodendroglia of MSA cases. Analysis of MSA brain tissue revealed depletion of regional signal for this transcript in many brain areas due to extensive neurodegeneration. Cellular analysis of oligodendroglia in crus cerebri, a GCI-rich region ventral to substantia nigra, revealed an absence of alpha-synuclein mRNA signal in control and MSA cases. However, an abundance of this transcript was detected in melanin-containing neurons of substantia nigra. Therefore, oligodendroglia do not express alpha-synuclein mRNA in control and MSA cases suggesting that involvement of alpha-synuclein in GCI pathology of MSA is due to its ectopic presence in oligodendroglia.
α-突触核蛋白是神经胶质细胞质包涵体(GCI)的主要成分,而GCI是多系统萎缩(MSA)的病理特征。我们之前已经证明,在正常人类大脑中,α-突触核蛋白mRNA具有局限的神经元表达模式,且无明显的神经胶质细胞表达。当前研究采用双标记原位杂交技术来确定α-突触核蛋白mRNA是否在MSA病例的少突胶质细胞中表达。对MSA脑组织的分析显示,由于广泛的神经退行性变,许多脑区该转录本的区域信号缺失。对黑质腹侧富含GCI的大脑脚少突胶质细胞进行细胞分析,结果显示在对照和MSA病例中均未检测到α-突触核蛋白mRNA信号。然而,在黑质含黑色素的神经元中检测到大量该转录本。因此,在对照和MSA病例中,少突胶质细胞不表达α-突触核蛋白mRNA,这表明α-突触核蛋白参与MSA的GCI病理过程是由于其在少突胶质细胞中的异位存在。