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损伤后周围神经修复中施万细胞可塑性的机制。

Mechanisms of Schwann cell plasticity involved in peripheral nerve repair after injury.

机构信息

Faculty of Biology, Institute of Developmental Biology and Neurobiology, Johannes Gutenberg University, Mainz, Germany.

出版信息

Cell Mol Life Sci. 2020 Oct;77(20):3977-3989. doi: 10.1007/s00018-020-03516-9. Epub 2020 Apr 10.

Abstract

The great plasticity of Schwann cells (SCs), the myelinating glia of the peripheral nervous system (PNS), is a critical feature in the context of peripheral nerve regeneration following traumatic injuries and peripheral neuropathies. After a nerve damage, SCs are rapidly activated by injury-induced signals and respond by entering the repair program. During the repair program, SCs undergo dynamic cell reprogramming and morphogenic changes aimed at promoting nerve regeneration and functional recovery. SCs convert into a repair phenotype, activate negative regulators of myelination and demyelinate the damaged nerve. Moreover, they express many genes typical of their immature state as well as numerous de-novo genes. These genes modulate and drive the regeneration process by promoting neuronal survival, damaged axon disintegration, myelin clearance, axonal regrowth and guidance to their former target, and by finally remyelinating the regenerated axon. Many signaling pathways, transcriptional regulators and epigenetic mechanisms regulate these events. In this review, we discuss the main steps of the repair program with a particular focus on the molecular mechanisms that regulate SC plasticity following peripheral nerve injury.

摘要

许旺细胞(Schwann cells,SCs)是周围神经系统(peripheral nervous system,PNS)的髓鞘形成胶质细胞,具有很强的可塑性,这是周围神经损伤和周围神经病变后再生的关键特征。在神经损伤后,SCs 会被损伤诱导信号迅速激活,并通过进入修复程序来做出反应。在修复程序中,SCs 经历动态的细胞重编程和形态发生变化,旨在促进神经再生和功能恢复。SCs 转变成修复表型,激活髓鞘形成的负调控因子,并对受损的神经进行脱髓鞘处理。此外,SCs 还表达许多其不成熟状态的典型基因以及许多新基因。这些基因通过促进神经元存活、损伤轴突解体、髓鞘清除、轴突再生和引导到其前靶标,并最终对再生轴突进行髓鞘化,来调节和驱动再生过程。许多信号通路、转录调节因子和表观遗传机制调节这些事件。在这篇综述中,我们讨论了修复程序的主要步骤,特别关注了周围神经损伤后调节 SC 可塑性的分子机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9099/11105056/00e61df602c9/18_2020_3516_Fig1_HTML.jpg

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