Department of Spine Surgery, Department of Orthopedics, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Mol Neurobiol. 2023 Sep;60(9):4983-4999. doi: 10.1007/s12035-023-03357-0. Epub 2023 May 20.
Abnormal expression of non-coding RNAs after spinal cord injury (SCI) is associated with pathophysiological outcomes. We bioinformatically predicted a circRNA-miRNA-mRNA axis in SCI. A total of 4690 mRNAs, 17 miRNAs, and 3928 circRNAs were differentially expressed, with co-expressed RNAs predicted to regulate pathways related to wound healing. Among the most highly differentially expressed circRNAs, circ_006573, but not circ_016395, weakened the viability and migration of rat aortic endothelial cells, and its biological effects were rescued with miR-376b-3p mimics. Furthermore, circ_006573 overexpression induced changes in Cebpb, IL-18, and Plscr1 expression that were reversed by miR-376b-3p. In a rat model, circ_006573 shRNA administration improved the pathological manifestations of SCI and ameliorated motor function. Moreover, the expression of CD31, CD34, and VEGF-A in spinal cord tissues was significantly elevated after circ_006573 shRNA treatment, indicating that circ_006573 may be involved in vascular regeneration and functional recovery after SCI. Thus, the circ_006573-miR-376b-3p axis offers a foundation for understanding pathophysiological mechanisms and predicting strategies for treating SCI.
脊髓损伤 (SCI) 后非编码 RNA 的异常表达与病理生理结果相关。我们通过生物信息学预测了 SCI 中的 circRNA-miRNA-mRNA 轴。共有 4690 个 mRNAs、17 个 miRNAs 和 3928 个 circRNAs 表达差异,共表达的 RNA 预测调节与伤口愈合相关的途径。在高度差异表达的 circRNAs 中,circ_006573 而非 circ_016395 降低了大鼠主动脉内皮细胞的活力和迁移能力,其生物学效应可通过 miR-376b-3p 模拟物恢复。此外,circ_006573 的过表达诱导了 Cebpb、IL-18 和 Plscr1 表达的变化,这些变化可被 miR-376b-3p 逆转。在大鼠模型中,circ_006573 shRNA 给药改善了 SCI 的病理表现并改善了运动功能。此外,circ_006573 shRNA 处理后脊髓组织中 CD31、CD34 和 VEGF-A 的表达显著升高,表明 circ_006573 可能参与 SCI 后的血管再生和功能恢复。因此,circ_006573-miR-376b-3p 轴为理解病理生理机制和预测 SCI 治疗策略提供了基础。