1 The International Center for Spinal Cord Injury, Hugo W. Moser Research Institute at Kennedy Krieger , Baltimore, Maryland.
2 Department of Neurology, Johns Hopkins University School of Medicine , Baltimore, Maryland.
J Neurotrauma. 2017 Dec 15;34(24):3351-3361. doi: 10.1089/neu.2016.4913. Epub 2017 Aug 10.
Myelination in the central nervous system (CNS) is a dynamic process that includes birth of oligodendrocyte progenitor cells (OPCs), their differentiation into oligodendrocytes, and ensheathment of axons. Regulation of myelination by neuronal activity has emerged as a new mechanism of CNS plasticity. Activity-dependent myelination has been shown to regulate sensory, motor, and cognitive functions. In this work, we aimed to employ this mechanism of CNS plasticity by utilizing induced neuronal activity to promote remyelination and functional recovery in a subchronic model of spinal cord injury (SCI). We used a mild contusive SCI at T10, which demyelinates surviving axons of the dorsal corticospinal tract (dCST), to investigate the effects of induced neuronal activity on oligodendrogenesis, remyelination, and motor function after SCI. Neuronal activity was induced through epidural electrodes that were implanted over the primary motor (M1) cortex. Induced neuronal activity increased the number of proliferating OPCs. Additionally, induced neuronal activity in the subchronic stages of SCI increased the number of oligodendrocytes, and enhanced myelin basic protein (MBP) expression and myelin sheath formation in dCST. The oligodendroglia regenerative response could have been mediated by axon-OPC synapses, the number of which increased after induced neuronal activity. Further, M1-induced neuronal activation promoted recovery of hindlimb motor function after SCI. Our work is a proof of principle demonstration that epidural electrical stimulation as a mode of inducing neuronal activity throughout white matter tracts of the CNS could be used to promote remyelination and functional recovery after CNS injuries and demyelination disorders.
中枢神经系统 (CNS) 的髓鞘形成是一个动态过程,包括少突胶质前体细胞 (OPC) 的产生、分化为少突胶质细胞以及轴突的包绕。神经元活动对髓鞘形成的调节已成为 CNS 可塑性的新机制。研究表明,活动依赖性髓鞘形成可调节感觉、运动和认知功能。在这项工作中,我们旨在利用 CNS 可塑性的这一机制,通过利用诱导的神经元活动来促进脊髓损伤 (SCI) 的亚慢性模型中的髓鞘再生和功能恢复。我们使用 T10 处的轻度挫伤性 SCI,使背侧皮质脊髓束 (dCST) 的存活轴突脱髓鞘,以研究诱导的神经元活动对 SCI 后少突胶质细胞发生、髓鞘再生和运动功能的影响。通过植入初级运动 (M1) 皮层上方的硬膜外电极来诱导神经元活动。诱导的神经元活动增加了增殖性 OPC 的数量。此外,SCI 亚慢性阶段的诱导神经元活动增加了少突胶质细胞的数量,并增强了 dCST 中的髓鞘碱性蛋白 (MBP) 表达和髓鞘形成。少突胶质细胞的再生反应可能是通过轴突-OPC 突触介导的,诱导神经元活动后,这种突触的数量增加。此外,M1 诱导的神经元激活促进了 SCI 后后肢运动功能的恢复。我们的工作证明了一个原理,即硬膜外电刺激作为一种在 CNS 白质束中诱导神经元活动的模式,可以用于促进 CNS 损伤和脱髓鞘疾病后的髓鞘再生和功能恢复。