Center for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY 14642, USA.
Center for Translational Neuromedicine and the Department of Neurology, University of Rochester Medical Center, Rochester, NY 14642, USA; Center for Translational Neuromedicine, University of Copenhagen, Copenhagen, Denmark.
Cell Rep. 2020 May 19;31(7):107658. doi: 10.1016/j.celrep.2020.107658.
Neonatally transplanted human glial progenitor cells (hGPCs) can myelinate the brains of myelin-deficient shiverer mice, rescuing their phenotype and survival. Yet, it has been unclear whether implanted hGPCs are similarly able to remyelinate the diffusely demyelinated adult CNS. We, therefore, ask if hGPCs could remyelinate both congenitally hypomyelinated adult shiverers and normal adult mice after cuprizone demyelination. In adult shiverers, hGPCs broadly disperse and differentiate as myelinating oligodendrocytes after subcortical injection, improving both host callosal conduction and ambulation. Implanted hGPCs similarly remyelinate denuded axons after cuprizone demyelination, whether delivered before or after demyelination. RNA sequencing (RNA-seq) of hGPCs back from cuprizone-demyelinated brains reveals their transcriptional activation of oligodendrocyte differentiation programs, while distinguishing them from hGPCs not previously exposed to demyelination. These data indicate the ability of transplanted hGPCs to disperse throughout the adult CNS, to broadly myelinate regions of dysmyelination, and also to be recruited as myelinogenic oligodendrocytes later in life, upon demyelination-associated demand.
新生期移植的人神经胶质前体细胞(hGPCs)可以使髓鞘缺失的颤抖小鼠大脑髓鞘化,从而挽救其表型和生存。然而,植入的 hGPCs 是否能够同样地使弥漫性脱髓鞘的成年中枢神经系统再髓鞘化仍不清楚。因此,我们想问 hGPCs 是否能够在成年后对先天低髓鞘化的颤抖者和正常成年小鼠进行再髓鞘化。在成年颤抖者中,hGPCs 在皮质下注射后广泛分散并分化为髓鞘形成的少突胶质细胞,改善了宿主胼胝体的传导和活动能力。植入的 hGPCs 在铜剥夺脱髓鞘后同样可以使裸露的轴突再髓鞘化,无论是在脱髓鞘之前还是之后。从铜剥夺脱髓鞘的大脑中返回的 hGPCs 的 RNA 测序(RNA-seq)揭示了它们对少突胶质细胞分化程序的转录激活,同时将其与以前未暴露于脱髓鞘的 hGPCs 区分开来。这些数据表明,移植的 hGPCs 具有在成年中枢神经系统中分散的能力,能够广泛地髓鞘化脱髓鞘区域,并且在脱髓鞘相关需求时,也能够在以后作为髓鞘形成的少突胶质细胞被招募。