1 Department of Rehabilitation Medicine, Yonsei University Wonju College of Medicine, Wonju, South Korea.
2 Department and Research Institute of Rehabilitation Medicine, Yonsei University College of Medicine, Seoul, South Korea.
Cell Transplant. 2017 Jul;26(7):1286-1300. doi: 10.1177/0963689717715822.
Spinal cord injury (SCI) is a devastating neurological disease. The pathophysiological mechanisms of SCI have been reported to be relevant to central nervous system injury such as brain injury. In this study, gene expression of the brain after SCI was elucidated using transcriptome analysis to characterize the temporal changes in global gene expression patterns in a SCI mouse model. Subjects were randomly classified into 3 groups: sham control, acute (3 h post-injury), and subacute (2 wk post-injury) groups. We sought to confirm the genes differentially expressed between post-injured groups and sham control group. Therefore, we performed transcriptome analysis to investigate the enriched pathways associated with pathophysiology of the brain after SCI using Database for Annotation Visualization, and Integrated Discovery (DAVID), which yielded Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway. Following enriched pathways were found in the brain: oxidative phosphorylation pathway; inflammatory response pathways-cytokine-cytokine receptor interaction and chemokine signaling pathway; and endoplasmic reticulum (ER) stress-related pathways-antigen processing and presentation and mitogen-activated protein kinase signaling pathway. Oxidative phosphorylation pathway was identified at acute phase, while inflammation response and ER stress-related pathways were identified at subacute phase. Since the following pathways-oxidative phosphorylation pathway, inflammatory response pathways, and ER stress-related pathways-have been well known in the SCI, we suggested a link between SCI and brain injury. These mechanisms provide valuable reference data for better understanding pathophysiological processes in the brain after SCI.
脊髓损伤(SCI)是一种毁灭性的神经疾病。据报道,SCI 的病理生理机制与脑损伤等中枢神经系统损伤有关。在这项研究中,使用转录组分析阐明了 SCI 后大脑的基因表达,以表征 SCI 小鼠模型中全局基因表达模式的时间变化。将研究对象随机分为 3 组:假手术对照组、急性(损伤后 3 小时)组和亚急性(损伤后 2 周)组。我们试图证实受伤组和假手术对照组之间差异表达的基因。因此,我们进行了转录组分析,使用数据库注释可视化和综合发现(DAVID)来研究与 SCI 后大脑病理生理学相关的富集途径,这产生了京都基因与基因组百科全书(KEGG)途径。在大脑中发现了以下富集途径:氧化磷酸化途径;炎症反应途径-细胞因子-细胞因子受体相互作用和趋化因子信号通路;内质网(ER)应激相关途径-抗原加工和呈递以及丝裂原激活蛋白激酶信号通路。氧化磷酸化途径在急性期被识别,而炎症反应和 ER 应激相关途径在亚急性期被识别。由于以下途径-氧化磷酸化途径、炎症反应途径和 ER 应激相关途径-在 SCI 中已被充分了解,我们提出了 SCI 与脑损伤之间的联系。这些机制为更好地理解 SCI 后大脑的病理生理过程提供了有价值的参考数据。