Jensen N A, Pedersen K M, Celis J E, West M J
Department of Medical Biochemistry, University of Aarhus, 8000 Aarhus C, Denmark.
J Clin Invest. 1998 Mar 15;101(6):1292-9. doi: 10.1172/JCI1807.
Pit, Oct, Unc (POU) homeo domain transcription factors have been implicated in various developmental processes, including cell division, differentiation, specification, and survival of specific cell types. Although expression of the transcription factor Oct-6 in oligodendroglia is confined to the promyelin stage and is downregulated at the myelin stage of development, the effect of Oct-6 overexpression on oligodendrocyte development has not been established. Here we show that transgenic animals overexpressing Oct-6 at late oligodendrocyte development develop a severe neurologic syndrome characterized by action tremors, recurrent seizures, and premature death. Axons in the central nervous system of Oct-6 transgenics were hypomyelinated, hypermyelinated, or dysmyelinated, and ultrastructural analyses suggested that myelin formation was premature. The vulnerability of developing oligodendroglia to Oct-6 deregulation provides evidence that the POU factor may play a direct role in myelin disease pathogenesis in the mammalian CNS.
POU(Pit、Oct、Unc)同源结构域转录因子参与了多种发育过程,包括特定细胞类型的细胞分裂、分化、特化和存活。尽管少突胶质细胞中转录因子Oct-6的表达局限于前髓鞘形成阶段,并在发育的髓鞘形成阶段下调,但Oct-6过表达对少突胶质细胞发育的影响尚未明确。在此我们表明,在少突胶质细胞发育后期过表达Oct-6的转基因动物会出现严重的神经综合征,其特征为动作性震颤、反复发作的癫痫和过早死亡。Oct-6转基因动物中枢神经系统中的轴突髓鞘形成不足、髓鞘过度形成或髓鞘形成异常,超微结构分析表明髓鞘形成过早。发育中的少突胶质细胞对Oct-6失调的易感性提供了证据,表明POU因子可能在哺乳动物中枢神经系统的髓鞘疾病发病机制中起直接作用。