Cheng Qiong, Wang Ya-Xian, Yu Jun, Yi Sheng
Key Laboratory of Neuroregeneration of Jiangsu and Ministry of Education, Co-innovation Center of Neuroregeneration, Nantong University, Nantong, Jiangsu Province, China.
Neural Regen Res. 2017 Jun;12(6):995-1002. doi: 10.4103/1673-5374.208596.
Wallerian degeneration is a critical biological process that occurs in distal nerve stumps after nerve injury. To systematically investigate molecular changes underlying Wallerian degeneration, we used a rat sciatic nerve transection model to examine microarray analysis outcomes and investigate significantly involved Kyoto Enrichment of Genes and Genomes (KEGG) pathways in injured distal nerve stumps at 0, 0.5, 1, 6, 12, and 24 hours, 4 days, 1, 2, 3, and 4 weeks after peripheral nerve injury. Bioinformatic analysis showed that only one KEGG pathway (cytokine-cytokine receptor interaction) was significantly enriched at an early time point (1 hour post-sciatic nerve transection). At later time points, the number of enriched KEGG pathways initially increased and then decreased. Three KEGG pathways were studied in further detail: cytokine-cytokine receptor interaction, neuroactive ligand-receptor interaction, and axon guidance. Moreover, temporal expression patterns of representative differentially expressed genes in these KEGG pathways were validated by real time-polymerase chain reaction. Taken together, the above three signaling pathways are important after sciatic nerve injury, and may increase our understanding of the molecular mechanisms underlying Wallerian degeneration.
沃勒变性是一种关键的生物学过程,发生在神经损伤后远端神经残端。为了系统地研究沃勒变性背后的分子变化,我们使用大鼠坐骨神经横断模型来检查微阵列分析结果,并研究在周围神经损伤后0、0.5、1、6、12和24小时、4天、1、2、3和4周时,受损远端神经残端中显著涉及的京都基因与基因组百科全书(KEGG)通路。生物信息学分析表明,在早期时间点(坐骨神经横断后1小时),只有一条KEGG通路(细胞因子-细胞因子受体相互作用)显著富集。在后期时间点,富集的KEGG通路数量最初增加,然后减少。对三条KEGG通路进行了更详细的研究:细胞因子-细胞因子受体相互作用、神经活性配体-受体相互作用和轴突导向。此外,通过实时聚合酶链反应验证了这些KEGG通路中代表性差异表达基因的时间表达模式。综上所述,上述三条信号通路在坐骨神经损伤后很重要,可能会增进我们对沃勒变性潜在分子机制的理解。