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首页> 外文期刊>Cell transplantation >Transplantation of a Peripheral Nerve with Neural Stem Cells Plus Lithium Chloride Injection Promote the Recovery of Rat Spinal Cord Injury
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Transplantation of a Peripheral Nerve with Neural Stem Cells Plus Lithium Chloride Injection Promote the Recovery of Rat Spinal Cord Injury

机译:用神经干细胞移植外周神经加上氯化锂注射液促进大鼠脊髓损伤的恢复

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摘要

Transplantation of neural stem cells (NSCs) holds great potential for the treatment of spinal cord injury (SCI). However, transplanted NSCs poorly survive in the SCI environment. We injected NSCs into tibial nerve and transplanted tibial nerve into a hemisected spinal cord and investigated the effects of lithium chloride (LiCI) on the survival of spinal neurons, axonal regeneration, and functional recovery. Our results show that most of the transplanted NSCs expressed glial fibrillary acidic protein, while there was no obvious expression of nestin, neuronal nuclei, or acetyltransferase found in NSCs. LiCI treatment produced less macrosialin (EDI) expression and axonal degeneration in tibial nerve after NSC injection. Our results also show that a regimen of LiCI treatment promoted NSC differentiation into NF200-positive neurons with neurite extension into the host spinal cord. The combination of tibial nerve transplantation with NSCs and LiCI injection resulted in more host motoneurons surviving in the spinal cord, more regenerated axons in tibial nerve, less glial scar area, and decreased ED I expression. We conclude that lithium may have therapeutic potential in cell replacement strategies for central nervous system injury due to its ability to promote survival and neuronal generation of grafted NSCs and reduced host immune reaction.
机译:神经干细胞的移植(NSCs)对脊髓损伤(SCI)的治疗具有很大的潜力。然而,在SCI环境中移植的NSCs存活不良。我们将NSCs注入胫骨神经和移植的胫骨神经分成脊髓,并研究了氯化锂(LICI)对脊髓神经元,轴突再生和功能性回收的生存的影响。我们的研究结果表明,大多数移植的NSCs表达了胶质纤维酸性蛋白质,而NSCs中没有明显表达巢蛋白,神经元核或乙酰转移酶。 LICI治疗在NSC注射后胫骨神经中的巨大巨粒素(EDI)表达和轴突变性。我们的研究结果还表明,Lici治疗方案促进了NSC分化成NF200阳性神经元,NF200阳性神经元具有神经沸石延伸进入宿主脊髓。胫骨神经移植与NSCs和LICI注射的组合导致脊髓中存活的更多宿主运动神经元,在胫骨神经中更加再生的轴突,少胶质瘢痕区域,并降低了ED I表达。我们得出结论,由于其促进移植的NSCs的存活和神经元产生和降低宿主免疫反应,因此锂可能具有中枢神经系统损伤的细胞更换策略中的治疗潜力。

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