首页> 外文期刊>Journal of biomedical materials research, Part A >Graft of the gelatin sponge scaffold containing genetically-modified neural stem cells promotes cell differentiation, axon regeneration, and functional recovery in rat with spinal cord transection
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Graft of the gelatin sponge scaffold containing genetically-modified neural stem cells promotes cell differentiation, axon regeneration, and functional recovery in rat with spinal cord transection

机译:含有遗传修饰神经干细胞的明胶海绵支架的移植促进细胞分化,轴突再生,以及脊髓横断术大鼠的功能恢复

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Biological materials combined with genetically-modified neural stem cells (NSCs) are candidate therapy targeting spinal cord injury (SCI). Based on our previous studies, here we performed gelatin sponge (GS) scaffold seeded with neurotrophin-3 (NT-3) and its receptor TrkC gene modifying NSCs for repairing SCI. Eight weeks later, compared with other groups, neurofilament-200 and 5-hydroxytryptamine positive nerve fibers were more in the injury site of the N+T-NSCs group. Immunofluorescence staining showed the grafted NSCs could differentiate into microtubule associated protein (Map2), postsynaptic density (PSD95), and mouse oligodendrocyte special protein (MOSP) positive cells. The percentage of the Map2, PSD95, and MOSP positive cells in the N+T-NSCs group was higher than the other groups. Immuno-electron microscopy showed the grafted NSCs making contact with each other in the injury site. Behavioral analysis indicated the recovery of hindlimbs locomotion was better in the groups receiving cell transplant, the best recovery was found in the N+T-NSCs group. Electrophysiology revealed the amplitude of cortical motor evoked potentials was increased significantly in the N+T-NSCs group, but the latency remained long. These findings suggest the GS scaffold containing genetically-modified NSCs may bridge the injury site, promote axon regeneration and partial functional recovery in SCI rats. (c) 2014 Wiley Periodicals, Inc. J Biomed Mater Res Part A: 103A: 1533-1545, 2015.
机译:生物材料与遗传修饰的神经干细胞(NSCs)结合鉴于脊髓损伤(SCI)的候选疗法。基于我们以前的研究,我们在这里进行了用神经营养蛋白-3(NT-3)的明胶海绵(GS)支架及其受体TRKC基因改性NSCs进行修复SCI。八周后,与其他群体相比,N + T-NSCs组的损伤部位有更多的血栓膜-200和5-羟基 - 羟基胺阳性神经纤维。免疫荧光染色显示接枝的NSC可以分化为微管相关蛋白(MAP2),突触突出度(PSD95)和小鼠少突胶细胞特殊蛋白(MOSP)阳性细胞。 N + T-NSCS组中MAP2,PSD95和MOSP阳性细胞的百分比高于其他组。免疫电子显微镜显示接枝的NSCs在损伤部位中彼此接触。行为分析表明,在接受细胞移植的基团中,在接受细胞移植的基团中,在群体中恢复的回收率,在N + T-NSCs组中发现了最佳恢复。电生理学揭示了N + T-NSCS组中皮质电机诱发电位的振幅,但延迟仍然存在长。这些发现表明GS支架含有遗传修饰的NSCs可以桥接损伤部位,促进SCI大鼠的轴突再生和部分功能恢复。 (c)2014 Wiley期刊,Inc。J生物保证金A部分:103A:1533-1545,2015。

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