Department of Nutrition, School of Public Health, Jilin University, 1163 Ximin Street, Changchun, China.
Life Sci. 2013 Oct 6;93(12-14):429-34. doi: 10.1016/j.lfs.2013.08.004. Epub 2013 Aug 22.
Oligodendrocyte/myelin abnormalities may be an important component of the pathogenesis found in schizophrenia. The aim of this current study was to examine the possible effects of the antipsychotic drugs (APDs) haloperidol (HAL), olanzapine (OLA), and quetiapine (QUE) on the development of oligodendroglial lineage cells.
CG4 cells, an oligodendrocyte progenitor cell line, were treated with various concentrations of HAL, OLA, or QUE for specific periods. The proliferation and differentiation of the CG4 cells were measured. The regulation of CG4 cell differentiation by oligodendrocyte lineage transcription factors 1 and 2 (Olig1 and Olig2) was examined.
The APDs used in this study had no effect on the proliferation of CG4 cells. The APDs elevated the expression of 2',3'-cyclic nucleotide 3'-phosphodiesterase (CNP), a specific marker of oligodendrocytes, and promoted the CG4 cells to differentiate into CNP positive oligodendrocytes. QUE and OLA increased the expression of both Olig1 and Olig2 whereas HAL only increased the expression of Olig2.
Our findings suggest that oligodendrocyte development is a target of HAL, OLA, and QUE and provide further evidence of the important role of oligodendrocytes in the pathophysiology and treatment of schizophrenia. They also indicate that the expression level of oligodendrocyte/myelin-related genes could be profoundly affected by APDs, which should be considered in future studies aiming to measure the oligodendrocyte/myelin-related gene expressions in schizophrenia patients.
少突胶质细胞/髓鞘异常可能是精神分裂症发病机制中的一个重要组成部分。本研究旨在探讨抗精神病药物(APD)氟哌啶醇(HAL)、奥氮平(OLA)和喹硫平(QUE)对少突胶质细胞谱系细胞发育的可能影响。
用不同浓度的 HAL、OLA 或 QUE 处理少突胶质前体细胞系 CG4 细胞一定时间。测量 CG4 细胞的增殖和分化。检测少突胶质细胞谱系转录因子 1 和 2(Olig1 和 Olig2)对 CG4 细胞分化的调节。
本研究中使用的 APD 对 CG4 细胞的增殖没有影响。APD 上调了寡核苷酸 2',3'-环核苷酸 3'-磷酸二酯酶(CNP)的表达,CNP 是少突胶质细胞的特异性标志物,并促进 CG4 细胞分化为 CNP 阳性少突胶质细胞。QUE 和 OLA 增加了 Olig1 和 Olig2 的表达,而 HAL 仅增加了 Olig2 的表达。
我们的研究结果表明,少突胶质细胞的发育是 HAL、OLA 和 QUE 的作用靶点,并为少突胶质细胞在精神分裂症的病理生理学和治疗中的重要作用提供了进一步的证据。它们还表明,少突胶质细胞/髓鞘相关基因的表达水平可能会受到 APD 的深刻影响,这在未来旨在测量精神分裂症患者少突胶质细胞/髓鞘相关基因表达的研究中应予以考虑。