Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48105, USA.
Department of Biomedical Engineering, University of Michigan, Ann Arbor, MI 48105, USA; Department of Biomedical Engineering, Northwestern University, Evanston, IL 60208, USA.
Mol Ther. 2018 Jul 5;26(7):1756-1770. doi: 10.1016/j.ymthe.2018.04.022. Epub 2018 Apr 27.
Trauma to the spinal cord and associated secondary inflammation can lead to permanent loss of sensory and motor function below the injury level, with the resulting environment serving as a barrier that limits regeneration. In this study, we investigate the localized expression of anti-inflammatory cytokines IL-10 and IL-4 via lentiviral transduction in multichannel bridges. Porous multichannel bridges provide physical guidance for axonal outgrowth with the cytokines hypothesized to modulate the neuroinflammatory microenvironment and enhance axonal regeneration. Gene expression analyses indicated that induced IL-10 and IL-4 expression decreased expression of pro-inflammatory genes and increased pro-regenerative genes relative to control. Moreover, these factors led to increased numbers of axons and myelination, with approximately 45% of axons myelinated and the number of oligodendrocyte myelinated axons significantly increased by 3- to 4-fold. Furthermore, the combination of a bridge with IL-10 and IL-4 expression improved locomotor function after injury to an average score of 6 relative to an average score of 3 for injury alone. Collectively, these studies highlight the potential for localized immunomodulation to decrease secondary inflammation and enhance regeneration that may have numerous applications.
脊髓损伤和相关的继发性炎症可导致损伤以下水平的感觉和运动功能永久丧失,由此产生的环境成为限制再生的障碍。在这项研究中,我们通过慢病毒转导研究了多通道桥中抗炎细胞因子 IL-10 和 IL-4 的局部表达。多孔多通道桥为轴突生长提供物理导向,细胞因子被假设可调节神经炎症微环境并增强轴突再生。基因表达分析表明,诱导的 IL-10 和 IL-4 表达降低了促炎基因的表达,增加了促再生基因的表达,与对照相比。此外,这些因子导致轴突数量和髓鞘形成增加,约有 45%的轴突髓鞘化,少突胶质细胞髓鞘化的轴突数量增加了 3 到 4 倍。此外,与单独损伤的平均 3 分相比,具有 IL-10 和 IL-4 表达的桥联合使用可改善损伤后的运动功能,平均评分为 6。总之,这些研究强调了局部免疫调节降低继发性炎症和增强再生的潜力,这可能有许多应用。