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调节周围神经髓鞘形成和施万细胞对损伤反应的信号。

Signals regulating myelination in peripheral nerves and the Schwann cell response to injury.

机构信息

Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, United States.

出版信息

Curr Opin Neurobiol. 2013 Dec;23(6):1041-8. doi: 10.1016/j.conb.2013.06.010. Epub 2013 Jul 26.

Abstract

In peripheral nerves, Schwann cells form myelin, which facilitates the rapid conduction of action potentials along axons in the vertebrate nervous system. Myelinating Schwann cells are derived from neural crest progenitors in a step-wise process that is regulated by extracellular signals and transcription factors. In addition to forming the myelin sheath, Schwann cells orchestrate much of the regenerative response that occurs after injury to peripheral nerves. In response to injury, myelinating Schwann cells dedifferentiate into repair cells that are essential for axonal regeneration, and then redifferentiate into myelinating Schwann cells to restore nerve function. Although this remarkable plasticity has long been recognized, many questions remain unanswered regarding the signaling pathways regulating both myelination and the Schwann cell response to injury.

摘要

在周围神经系统中,施万细胞形成髓鞘,这有助于动作电位沿着脊椎动物神经系统中的轴突快速传导。少突胶质细胞是由神经嵴祖细胞逐步分化而来的,这个过程受到细胞外信号和转录因子的调节。除了形成髓鞘外,施万细胞还协调周围神经损伤后发生的大部分再生反应。作为对损伤的反应,髓鞘形成的施万细胞去分化为修复细胞,这对于轴突再生是必不可少的,然后再重新分化为髓鞘形成的施万细胞,以恢复神经功能。尽管这种显著的可塑性早已被认识到,但关于调节髓鞘形成和施万细胞对损伤反应的信号通路,仍有许多问题尚未得到解答。

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