Departments of Cell Biology and Human Anatomy, University of California, Davis, Sacramento, California 95817, USA.
Sci Rep. 2011;1:2. doi: 10.1038/srep00002. Epub 2011 Jun 14.
Basic helix-loop-helix transcription factors Olig1 and Olig2 critically regulate oligodendrocyte development. Initially identified as a downstream effector of Olig1, an oligodendrocyte-specific zinc finger transcription repressor, Zfp488, cooperates with Olig2 function. Although Zfp488 is required for oligodendrocyte precursor formation and differentiation during embryonic development, its role in oligodendrogenesis of adult neural progenitor cells is not known. In this study, we tested whether Zfp488 could promote an oligodendrogenic fate in adult subventricular zone (SVZ) neural stem/progenitor cells (NSPCs). Using a cuprizone-induced demyelination model in mice, we examined the effect of retrovirus-mediated Zfp488 overexpression in SVZ NSPCs. Our results showed that Zfp488 efficiently promoted the differentiation of the SVZ NSPCs into mature oligodendrocytes in vivo. After cuprizone-induced demyelination injury, Zfp488-transduced mice also showed significant restoration of motor function to levels comparable to control mice. Together, these findings identify a previously unreported role for Zfp488 in adult oligodendrogenesis and functional remyelination after injury.
碱性螺旋-环-螺旋转录因子 Olig1 和 Olig2 对少突胶质细胞的发育起关键作用。最初被鉴定为少突胶质细胞特异性锌指转录抑制因子 Olig1 的下游效应物,Zfp488 与 Olig2 功能合作。虽然 Zfp488 在胚胎发育过程中少突胶质前体细胞的形成和分化中是必需的,但它在成年神经祖细胞中的少突胶质发生中的作用尚不清楚。在这项研究中,我们测试了 Zfp488 是否可以促进成年侧脑室下区 (SVZ) 神经干细胞/祖细胞 (NSPC) 中的少突胶质细胞命运。我们使用在小鼠中诱导脱髓鞘的 cuprizone 模型,研究了 SVZ NSPC 中逆转录病毒介导的 Zfp488 过表达的效果。我们的结果表明,Zfp488 有效地促进了 SVZ NSPC 体内向成熟少突胶质细胞的分化。在 cuprizone 诱导的脱髓鞘损伤后,转导 Zfp488 的小鼠的运动功能也显著恢复到与对照小鼠相当的水平。总之,这些发现确定了 Zfp488 在成年少突胶质细胞发生和损伤后功能髓鞘形成中的一个以前未报道的作用。