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施万细胞发育和神经再生中的转录抑制

Transcriptional inhibition in Schwann cell development and nerve regeneration.

作者信息

Quintes Susanne, Brinkmann Bastian G

机构信息

Max-Planck-Institute of Experimental Medicine, Department of Neurogenetics, Göttingen, Germany.

Department of Clinical Neurophysiology, University Medical Center Göttingen (UMG), Göttingen, Germany.

出版信息

Neural Regen Res. 2017 Aug;12(8):1241-1246. doi: 10.4103/1673-5374.213537.

Abstract

Schwann cells, the myelinating glial cells of the peripheral nervous system are remarkably plastic after nerve trauma. Their transdifferentiation into specialized repair cells after injury shares some features with their development from the neural crest. Both processes are governed by a tightly regulated balance between activators and inhibitors to ensure timely lineage progression and allow re-maturation after nerve injury. Functional recovery after injury is very successful in rodents, however, in humans, lack of regeneration after nerve trauma and loss of function as the result of peripheral neuropathies represents a significant problem. Our understanding of the basic molecular machinery underlying Schwann cell maturation and plasticity has made significant progress in recent years and novel players have been discovered. While the transcriptional activators of Schwann cell development and nerve repair have been well defined, the mechanisms counteracting negative regulation of (re-)myelination are less well understood. Recently, transcriptional inhibition has emerged as a new regulatory mechanism in Schwann cell development and nerve repair. This mini-review summarizes some of the regulatory mechanisms controlling both processes and the novel concept of "inhibiting the inhibitors" in the context of Schwann cell plasticity.

摘要

施万细胞是周围神经系统的髓鞘形成神经胶质细胞,在神经损伤后具有显著的可塑性。它们在损伤后转分化为特殊的修复细胞,这一过程与它们从神经嵴发育而来有一些共同特征。这两个过程都受激活剂和抑制剂之间严格调控的平衡支配,以确保谱系及时进展,并使神经损伤后能够重新成熟。在啮齿动物中,损伤后的功能恢复非常成功,然而,在人类中,神经损伤后缺乏再生以及周围神经病变导致的功能丧失是一个重大问题。近年来,我们对施万细胞成熟和可塑性的基本分子机制的理解取得了重大进展,并且发现了新的相关分子。虽然施万细胞发育和神经修复的转录激活剂已经得到很好的定义,但对抗(再)髓鞘形成负调控的机制却了解较少。最近,转录抑制已成为施万细胞发育和神经修复中的一种新调控机制。这篇综述总结了一些控制这两个过程的调控机制,以及施万细胞可塑性背景下“抑制抑制剂”的新概念。

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