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体内递送 STC2 基因促进坐骨神经轴突再生。

In Vivo Gene Delivery of STC2 Promotes Axon Regeneration in Sciatic Nerves.

机构信息

Department of Life Sciences, Lab of Axon Regeneration & Degeneration, Korea University, Anam-ro 145, Seongbuk-gu, Seoul, 02841, Republic of Korea.

Department of Molecular Neuroscience, Dong-A University College of Medicine, Busan, 49201, Republic of Korea.

出版信息

Mol Neurobiol. 2021 Feb;58(2):750-760. doi: 10.1007/s12035-020-02155-2. Epub 2020 Oct 4.

Abstract

Neurons are vulnerable to injury, and failure to activate self-protective systems after injury leads to neuronal death. However, sensory neurons in dorsal root ganglions (DRGs) mostly survive and regenerate their axons. To understand the mechanisms of the neuronal injury response, we analyzed the injury-responsive transcriptome and found that Stc2 is immediately upregulated after axotomy. Stc2 is required for axon regeneration in vivo and in vitro, indicating that Stc2 is a neuronal factor regulating axonal injury response. The application of the secreted stanniocalcin 2 to injured DRG neurons promotes regeneration. Stc2 thus represents a potential secretory protein with a feedback function regulating regeneration. Finally, the in vivo gene delivery of STC2 increases regenerative growth after injury in peripheral nerves in mice. These results suggest that Stc2 is an injury-responsive gene required for axon regeneration and a potential target for developing therapeutic applications.

摘要

神经元容易受到损伤,而损伤后自我保护系统未能激活会导致神经元死亡。然而,背根神经节(DRG)中的感觉神经元大多存活并再生其轴突。为了了解神经元损伤反应的机制,我们分析了损伤反应转录组,发现轴突切断后 Stc2 立即上调。Stc2 对于体内和体外的轴突再生是必需的,这表明 Stc2 是一种调节轴突损伤反应的神经元因子。将分泌的 Stc2 应用于损伤的 DRG 神经元可促进再生。因此,Stc2 代表了一种具有反馈功能的潜在分泌蛋白,可调节再生。最后,体内基因传递 STC2 可增加小鼠周围神经损伤后的再生性生长。这些结果表明,Stc2 是一种对轴突再生必需的损伤反应基因,也是开发治疗应用的潜在靶点。

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