Laboratory of Axon Regeneration & Degeneration, Department of Life Sciences, Korea University, Seoul, Korea.
FEBS J. 2021 Aug;288(16):4786-4797. doi: 10.1111/febs.15646. Epub 2020 Dec 9.
Axons are vulnerable to injury, potentially leading to degeneration or neuronal death. While neurons in the central nervous system fail to regenerate, neurons in the peripheral nervous system are known to regenerate. Since it has been shown that injury-response signal transduction is mediated by gene expression changes, expression profiling is a useful tool to understand the molecular mechanisms of regeneration. Axon regeneration is regulated by injury-responsive genes induced in both neurons and their surrounding non-neuronal cells. Thus, an experimental setup for the comparative analysis between regenerative and nonregenerative conditions is essential to identify ideal targets for the promotion of regeneration-associated genes and to understand the mechanisms of axon regeneration. Here, we review the original research that shows the key factors regulating axon regeneration, in particular by using comparative gene expression profiling in diverse systems.
轴突容易受伤,可能导致退化或神经元死亡。虽然中枢神经系统的神经元不能再生,但周围神经系统的神经元可以再生。由于已经表明,损伤反应信号转导是由基因表达变化介导的,因此表达谱分析是理解再生分子机制的有用工具。轴突再生受神经元及其周围非神经元细胞中诱导的损伤反应基因调控。因此,建立再生和非再生条件之间的比较分析实验设置对于鉴定促进与再生相关基因的理想靶标以及理解轴突再生机制至关重要。在这里,我们综述了原始研究,这些研究表明了调节轴突再生的关键因素,特别是通过在不同系统中使用比较基因表达谱分析。