少突胶质细胞
双相情感障碍
精神分裂症(面向对象编程)
微阵列
微阵列分析技术
髓鞘
基因表达
生物
基因
神经科学
心理学
遗传学
精神科
中枢神经系统
认知
作者
Dmitri Tkachev,Michael L. Mimmack,Margaret M. Ryan,Matthew T. Wayland,Tom P. Freeman,Peter B. Jones,Michael P. Starkey,Maree J. Webster,Robert H. Yolken,Sabine Bahn
出处
期刊:The Lancet
[Elsevier]
日期:2003-09-01
卷期号:362 (9386): 798-805
被引量:904
标识
DOI:10.1016/s0140-6736(03)14289-4
摘要
Results of array studies have suggested abnormalities in expression of lipid and myelin-related genes in schizophrenia. Here, we investigated oligodendrocyte-specific and myelination-associated gene expression in schizophrenia and bipolar affective disorder.We used samples from the Stanley brain collection, consisting of 15 schizophrenia, 15 bipolar affective disorder, and 15 control brains. Indexing-based differential display PCR was done to screen for differences in gene expression in schizophrenia patients versus controls. Results were cross-validated with quantitative PCR, which was also used to investigate expression profiles of 16 other oligodendrocyte and myelin genes in schizophrenia and bipolar disorder. These genes were further investigated with an ongoing microarray analysis.Results of differential display and quantitative PCR analysis showed a reduction of key oligodendrocyte-related and myelin-related genes in schizophrenia and bipolar patients; expression changes for both disorders showed a high degree of overlap. Microarray results of the same genes investigated by quantitative PCR correlated well overall.Schizophrenia and bipolar brains showed downregulation of key oligodendrocyte and myelination genes, including transcription factors that regulate these genes, compared with control brains. These results lend support to and extend observations from other microarray investigations. Our study also showed similar expression changes to the schizophrenia group in bipolar brains, which thus lends support to the notion that the disorders share common causative and pathophysiological pathways.
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