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首页> 外文期刊>The Journal of Neuroscience: The Official Journal of the Society for Neuroscience >Peripheral nervous system progenitors can be reprogrammed to produce myelinating oligodendrocytes and repair brain lesions.
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Peripheral nervous system progenitors can be reprogrammed to produce myelinating oligodendrocytes and repair brain lesions.

机译:周围神经系统祖细胞可以重新编程以产生髓鞘少突胶质细胞并修复脑损伤。

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摘要

Neural crest stem cells (NCSCs) give rise to the neurons and glia of the peripheral nervous system (PNS). NCSC-like cells can be isolated from multiple peripheral organs and maintained in neurosphere culture. Combining in vitro culture and transplantation, we show that expanded embryonic NCSC-like cells lose PNS traits and are reprogrammed to generate CNS cell types. When transplanted into the embryonic or adult mouse CNS, they differentiate predominantly into cells of the oligodendrocyte lineage without any signs of tumor formation. NCSC-derived oligodendrocytes generate CNS myelin and contribute to the repair of the myelin deficiency in shiverer mice. These results demonstrate a reprogramming of PNS progenitors to CNS fates without genetic modification and imply that PNS cells could be a potential source for cell-based CNS therapy.
机译:神经c干细胞(NCSC)产生周围神经系统(PNS)的神经元和神经胶质。可以从多个周围器官中分离出类似NCSC的细胞,并将其保存在神经球培养物中。结合体外培养和移植,我们显示扩大的胚胎NCSC样细胞失去PNS性状,并重新编程以生成CNS细胞类型。当移植到胚胎或成年小鼠CNS中时,它们主要分化为少突胶质细胞谱系的细胞,而没有任何肿瘤形成的迹象。 NCSC衍生的少突胶质细胞产生CNS髓磷脂,并有助于修复颤抖小鼠的髓磷脂缺乏症。这些结果表明,PNS祖细胞无需进行基因改造即可重编程为CNS命运,这意味着PNS细胞可能是基于细胞的CNS治疗的潜在来源。

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