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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >A Subpopulation of Foxj1-Expressing, Nonmyelinating Schwann Cells of the Peripheral Nervous System Contribute to Schwann Cell Remyelination in the Central Nervous System
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A Subpopulation of Foxj1-Expressing, Nonmyelinating Schwann Cells of the Peripheral Nervous System Contribute to Schwann Cell Remyelination in the Central Nervous System

机译:外周神经系统的表达福克斯J1表达的亚群,促进了中枢神经系统中的施曼细胞髓髓

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New myelin sheaths can be restored to demyelinated axons in a spontaneous regenerative process called remyelination. In general, new myelin sheaths are made by oligodendrocytes newly generated from a widespread population of adult CNS progenitors called oligodendrocyte progenitor cells (OPCs). New myelin in CNS remyelination in both experimental models and clinical diseases can also be generated by Schwann cells (SCs), the myelin-forming cells of the PNS. Fate-mapping studies have shown that SCs contributing to remyelination in the CNS are often derived from OPCs and appear not to be derived from myelinating SCs from the PNS. In this study, we address whether CNS remyelinating SCs can also be generated from PNS-derived cells other than myelinating SCs. Using a genetic fate-mapping approach, we have found that a subpopulation of nonmyelinating SCs identified by the expression of the transcription factor Foxj1 also contribute to CNS SC remyelination, as well as to remyelination in the PNS. We also find that the ependymal cells lining the central canal of the spinal cord, which also express Foxj1, do not generate cells that contribute to CNS remyelination. These findings therefore identify a previously unrecognized population of PNS glia that can participate in the regeneration of new myelin sheaths following CNS demyelination.
机译:新的髓鞘可以在被称为remyelinal的自发再生过程中恢复到脱髓鞘轴突中。通常,新的髓鞘是由新的寡核细胞从名为少突胶质细胞祖细胞(OPCS)的成年CNS祖细胞群的广泛群体新产生。在实验模型和临床疾病中的CNS重新髓鞘中的新髓鞘也可以由Schwann细胞(SCS)产生PNS的髓鞘细胞。命运映射研究表明,CNS中贡献的SCS往往源自OPCS,并且看起来不会从PNS中源自髓鞘SCS。在这项研究中,我们解决了CNS重新链接SCS的CNS雷米序列SC是否也可以从髓鞘之外的PNS衍生的细胞中产生。使用遗传命运映射方法,我们发现通过转录因子FoxJ1的表达鉴定的非混蛋SC的亚群也有助于CNS SC重新髓鞘,以及PNS中的重新髓鞘。我们还发现,脊髓中央管道的突出突变细胞,其也表达FoxJ1,不会产生有助于CNS重新髓鞘的细胞。因此,这些结果鉴定了先前未被识别的PNS胶质群人群,可以在CNS脱髓鞘后参与新的髓鞘鞘的再生。

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