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首页> 外文期刊>CNS neuroscience & therapeutics. >Local injection of Lenti‐Olig2 at lesion site promotes functional recovery of spinal cord injury in rats
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Local injection of Lenti‐Olig2 at lesion site promotes functional recovery of spinal cord injury in rats

机译:在病变部位局部注射Lenti-Olig2可促进大鼠脊髓损伤的功能恢复

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Summary AimsOlig2 is one of the most critical factors during CNS development, which belongs to b-HLH transcription factor family. Previous reports have shown that Olig2 regulates the remyelination processes in CNS demyelination diseases models. However, the role of Olig2 in contusion spinal cord injury (SCI) and the possible therapeutic effects remain obscure. This study aims to investigate the effects of overexpression Olig2 by lentivirus on adult spinal cord injury rats. MethodsLenti-Olig2 expression and control Lenti-eGFP vectors were prepared, and virus in a total of 5?μL (108 TU/mL) was locally injected into the injured spinal cord 1.5?mm rostral and caudal near the epicenter. Immunostaining, Western blot, electron microscopy, and CatWalk analyzes were employed to investigate the effects of Olig2 on spinal cord tissue repair and functional recovery. ResultsInjection of Lenti-Olig2 significantly increased the number of oligodendrocytes lineage cells and enhanced myelination after SCI. More importantly, the introduction of Olig2 greatly improved hindlimb locomotor performances. Other oligodendrocyte-related transcription factors, which were downregulated or upregulated after injury, were reversed by Olig2 induction. ConclusionsOur findings provided the evidence that overexpression Olig2 promotes myelination and locomotor recovery of contusion SCI, which gives us more understanding of Olig2 on spinal cord injury treatment.
机译:总结AimsOlig2是CNS发育过程中最关键的因素之一,属于b-HLH转录因子家族。先前的报道表明,Olig2调节中枢神经系统脱髓鞘疾病模型中的髓鞘再生过程。但是,Olig2在挫伤性脊髓损伤(SCI)中的作用以及可能的治疗效果仍然不清楚。这项研究旨在调查慢病毒过表达Olig2对成年脊髓损伤大鼠的影响。方法制备Lenti-Olig2表达载体和对照Lenti-eGFP载体,将病毒共5?μL(108 TU / mL)局部注入震中中心附近1.5?mm的受损脊髓尾端和尾端。免疫染色,蛋白质印迹,电子显微镜和CatWalk分析被用来研究Olig2对脊髓组织修复和功能恢复的影响。结果注射Lenti-Olig2可显着增加SCI后少突胶质细胞谱系细胞的数量并增强髓鞘形成。更重要的是,Olig2的引入极大地改善了后肢的运动性能。 Olig2诱导可逆转其他与少突胶质细胞相关的转录因子,这些转录因子在损伤后被下调或上调。结论我们的发现为过度表达Olig2促进挫伤性脊髓损伤的髓鞘形成和运动恢复提供了证据,这使我们对Olig2在脊髓损伤治疗中有了更多的了解。

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