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Genetic programs and responses of neural stem/progenitor cells during demyelination: potential insights into repair mechanisms in multiple sclerosis

机译:脱髓鞘过程中神经干/祖细胞的遗传程序和反应:对多发性硬化症修复机制的潜在见解

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摘要

In recent years, it has become evident that the adult mammalian CNS contains a population of neural stem cells (NSCs) described as immature, undifferentiated, multipotent cells, that may be called upon for repair in neurodegenerative and demyelinating diseases. NSCs may give rise to oligodendrocyte progenitor cells (OPCs) and other myelinating cells. This article reviews recent progress in elucidating the genetic programs and dynamics of NSC and OPC proliferation, differentiation, and apoptosis, including the response to demyelination. Emerging knowledge of the molecules that may be involved in such responses may help ion the design of future stem cell based treatment of demyelinating diseases such as multiple sclerosis.
机译:近年来,很明显,成年哺乳动物中枢神经系统含有一群神经干细胞(NSC),被描述为不成熟的,未分化的多能细胞,可被要求修复神经退行性疾病和脱髓鞘疾病。 NSC可能会产生少突胶质细胞祖细胞(OPC)和其他髓鞘细胞。本文回顾了阐明NSC和OPC增殖,分化和凋亡的遗传程序和动力学的最新进展,包括对脱髓鞘的反应。可能参与此类反应的分子的新兴知识可能有助于设计未来基于干细胞的脱髓鞘疾病(例如多发性硬化)的治疗设计。

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