首页> 外文期刊>Journal of neurotrauma >Induced Neural Activity Promotes an Oligodendroglia Regenerative Response in the Injured Spinal Cord and Improves Motor Function after Spinal Cord Injury
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Induced Neural Activity Promotes an Oligodendroglia Regenerative Response in the Injured Spinal Cord and Improves Motor Function after Spinal Cord Injury

机译:诱导的神经活性促进受伤脊髓中的少突胚胎再生反应,并在脊髓损伤后改善电机功能

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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.
机译:中枢神经系统(CNS)中的髓鞘是一种动态过程,包括少突胶质细胞祖细胞(OPCS)的诞生,它们分化为少突胶质细胞,以及轴突的缠结。神经元活性对髓鞘产生的调节作为CNS可塑性的新机制。已显示活动依赖性髓鞘调节感官,电动机和认知功能。在这项工作中,我们旨在通过利用诱导的神经元活性来促进脊髓损伤次级损伤(SCI)的次级调整模型中的髓鞘化和功能恢复来使用这种CNS塑性机制。我们在T10使用温和的旨在的SCI,该SCI在T10进行了Demyninate背心脊髓椎间盘(DCST)的存活轴突,以探讨诱导神经元活性对SCI后脱霉菌的作用。通过植入初级马达(M1)皮质的硬膜外电极诱导神经元活性。诱发的神经元活性增加了增殖OPC的数量。另外,在SCI的亚形级阶段的诱导神经元活性增加了DCST中的少突胶质细胞的数量,提高了髓鞘碱性蛋白(MBP)表达和髓鞘形成。可以通过Axon-OPC突触介导的少突胚胎再生反应,其诱导神经元活性后增加的数量。此外,M1诱导的神经元激活促进了SCI后的后肢电机功能的回收率。我们的作品是原则示范的证据,即硬膜外电刺激作为诱导CNS的白种物质诱导的神经元活动的模式可用于促进CNS损伤和脱髓鞘后患者的核化和功能恢复。

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