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髓鞘发育的调控

Regulation of myelin development.

作者信息

Kamholz J A

机构信息

Department of Neurology, Wayne State University School of Medicine, Detroit, Michigan, USA.

出版信息

Mult Scler. 1996 Dec;2(5):236-40. doi: 10.1177/135245859600200506.

Abstract

During the final stage of oligodendrocyte differentiation, oligodendrocyte precursors cease proliferating, and coordinately activate the set of genes encoding the myelin-specific structural proteins. Two homeodomain-containing transcription factors, SCIP and Gtx, by virtue of their temporal patterns of expression, are implicated in the regulation of this process. SCIP is expressed in dividing oligodendrocyte precursors, and its expression is downregulated prior to the onset of oligodendrocyte differentiation. Gtx, in contrast, is expressed in post-mitotic, differentiated oligodendrocytes, and its expression parallels that of the myelin-specific mRNA in a variety of physiologically relevant circumstances. In addition, Gtx binds to several sites within the MBP, PLP and Gtx promoters in a sequence-specific manner probably by way of the core homeodomain binding motif. A third transcription factor, NFI, is also important for oligodendrocyte-specific gene expression, since it turns off myelin gene expression in non-myelinating cells. These three transcription factors are thus important for the normal process of oligodendrocyte differentiation and myelination, and may be involved in the molecular pathogenesis of both demyelination and remyelination in multiple sclerosis.

摘要

在少突胶质细胞分化的最后阶段,少突胶质细胞前体细胞停止增殖,并协同激活一组编码髓鞘特异性结构蛋白的基因。两种含同源结构域的转录因子,即SCIP和Gtx,凭借其表达的时间模式,参与了这一过程的调控。SCIP在正在分裂的少突胶质细胞前体细胞中表达,其表达在少突胶质细胞分化开始前下调。相反,Gtx在有丝分裂后的分化少突胶质细胞中表达,在多种生理相关情况下,其表达与髓鞘特异性mRNA的表达平行。此外,Gtx可能通过核心同源结构域结合基序以序列特异性方式结合到MBP、PLP和Gtx启动子内的多个位点。第三种转录因子NFI对少突胶质细胞特异性基因表达也很重要,因为它在非髓鞘形成细胞中关闭髓鞘基因表达。因此,这三种转录因子对少突胶质细胞分化和髓鞘形成的正常过程很重要,可能参与了多发性硬化症中脱髓鞘和再髓鞘形成的分子发病机制。

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