Wang Xin-Liang, Wang Zong-Yi, Chen Xing-Han, Cai Yuan, Hu Bing
Chinese Academy of Sciences Key Laboratory of Brain Function and Disease, Hefei National Research Center for Physical Sciences at the Microscale, University of Science and Technology of China, Hefei, 230026, China.
First Affiliated Hospital of USTC, School of Life Sciences, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, 230026, China.
Neurosci Bull. 2025 Apr;41(4):633-648. doi: 10.1007/s12264-024-01329-5. Epub 2024 Dec 8.
Acute mitochondrial damage and the energy crisis following axonal injury highlight mitochondrial transport as an important target for axonal regeneration. Syntaphilin (Snph), known for its potent mitochondrial anchoring action, has emerged as a significant inhibitor of both mitochondrial transport and axonal regeneration. Therefore, investigating the molecular mechanisms that influence the expression levels of the snph gene can provide a viable strategy to regulate mitochondrial trafficking and enhance axonal regeneration. Here, we reveal the inhibitory effect of microRNA-146b (miR-146b) on the expression of the homologous zebrafish gene syntaphilin b (snphb). Through CRISPR/Cas9 and single-cell electroporation, we elucidated the positive regulatory effect of the miR-146b-snphb axis on Mauthner cell (M-cell) axon regeneration at the global and single-cell levels. Through escape response tests, we show that miR-146b-snphb signaling positively regulates functional recovery after M-cell axon injury. In addition, continuous dynamic imaging in vivo showed that reprogramming miR-146b significantly promotes axonal mitochondrial trafficking in the pre-injury and early stages of regeneration. Our study reveals an intrinsic axonal regeneration regulatory axis that promotes axonal regeneration by reprogramming mitochondrial transport and anchoring. This regulation involves noncoding RNA, and mitochondria-associated genes may provide a potential opportunity for the repair of central nervous system injury.
轴突损伤后的急性线粒体损伤和能量危机凸显了线粒体运输作为轴突再生的重要靶点。突触亲和素(Snph)以其强大的线粒体锚定作用而闻名,已成为线粒体运输和轴突再生的重要抑制剂。因此,研究影响snph基因表达水平的分子机制可为调节线粒体运输和促进轴突再生提供可行策略。在此,我们揭示了微小RNA-146b(miR-146b)对斑马鱼同源基因突触亲和素b(snphb)表达的抑制作用。通过CRISPR/Cas9和单细胞电穿孔技术,我们在整体和单细胞水平上阐明了miR-146b-snphb轴对毛特纳细胞(M细胞)轴突再生的正向调节作用。通过逃避反应测试,我们发现miR-146b-snphb信号通路对M细胞轴突损伤后的功能恢复具有正向调节作用。此外,体内连续动态成像显示,重编程miR-146b可在损伤前和再生早期显著促进轴突线粒体运输。我们的研究揭示了一种内在的轴突再生调节轴,该轴通过重编程线粒体运输和锚定来促进轴突再生。这种调节涉及非编码RNA,线粒体相关基因可能为中枢神经系统损伤的修复提供潜在机会。