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Human neural stem cells promote corticospinal axons regeneration and synapse reformation in injured spinal cord of rats

机译:人类神经干细胞促进大鼠脊髓损伤中皮质脊髓轴突的再生和突触的重建。

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Background Axonal regeneration in lesioned mammalian central nervous system is abortive, and this causes permanent disabilities in individuals with spinal cord injuries. This paper studied the action of neural stem cell (NSC) in promoting corticospinal axons regeneration and synapse reformation in rats with injured spinal cord. Methods NSCs were isolated from the cortical tissue of spontaneous aborted human fetuses in accordance with the ethical request. The cells were discarded from the NSC culture to acquire NSC-conditioned medium. Sixty adult Wistar rats were randomly divided into four groups (n=15 in each): NSC graft, NSC medium, graft control and medium control groups. Microsurgical transection of the spinal cord was performed in all the rats at the T11. The NSC graft group received stereotaxic injections of NSCs suspension into both the spinal cord stumps immediately after transection; graft control group received DMEM injection. In NSC medium group, NSC-conditioned medium was administered into the spinal cord every week; NSC culture medium was administered to the medium control group. Hindlimb motor function was assessed using the BBB Locomotor Rating Scale. Regeneration of biotin dextran amine (BDA) labeled corticospinal tract was assessed. Differentiation of NSCs and the expression of synaptophysin at the distal end of the injured spinal cord were observed under a confocal microscope. Group comparisons of behavioral data were analyzed with ANOVA. Results NSCs transplantation resulted in extensive growth of corticospinal axons and locomotor recovery in adult rats after complete spinal cord transection, the mean BBB scores reached 12.5 in NSC graft group and 2.5 in graft control group (P < 0.05). There was also significant difference in BBB score between the NSC medium (11.7) and medium control groups (3.7, P < 0.05). BDA traces regenerated fibers sprouted across the lesion site and entered the caudal part of the spinal cord. Synaptophysin expression colocalized with BDA positive axons and neurons distal to the injury site. Transplanted cells were found to migrate into the lesion, but not scatter along the route of axon grows. The cells differentiated into astrocytes or oligodendrocytes, but not into the neurons after transplantation. Furthermore, NSC medium administration did not limit the degree of axon sprouting and functional recovery of the injured rats compared to the NSC graft group. Conclusions Human embryonic neural stem cells can promote functional corticospinal axons regeneration and synapse reformation in the injured spinal cord of rats. The action is mainly through the nutritional effect of the stem cells on the spinal cord.
机译:背景技术病变哺乳动物中枢神经系统中的轴突再生是流产的,这会导致脊髓损伤的人永久性残疾。本文研究了神经干细胞(NSC)在脊髓损伤大鼠中促进皮质脊髓轴突再生和突触重构的作用。方法按照伦理要求,从自然流产的胎儿的皮层组织中分离出神经干细胞。从NSC培养物中丢弃细胞以获得NSC条件培养基。 60只成年Wistar大鼠随机分为四组(每组n = 15):NSC移植物,NSC培养基,移植物对照组和培养基对照组。在T11时在所有大鼠中进行脊髓的显微外科手术横切。横断后,NSC移植组立即将立体定向的NSC悬浮液注射入两个脊髓残端。移植对照组接受DMEM注射。在NSC培养基组中,每周将NSC条件培养基注入脊髓中。将NSC培养基给予培养基对照组。后肢运动功能使用BBB机能评定量表进行评估。评估了生物素葡聚糖胺(BDA)标记的皮质脊髓束的再生。在共聚焦显微镜下观察到神经干细胞的分化和受损脊髓远端突触素的表达。使用方差分析分析行为数据的分组比较。结果NSCs移植导致成年大鼠完全脊髓横断后皮质脊髓轴突的广泛生长和运动恢复,NSC移植组的BBB平均得分分别达到12.5和2.5(P <0.05)。 NSC培养基(11.7)和培养基对照组之间的BBB评分也有显着差异(3.7,P <0.05)。 BDA痕迹再生的纤维发芽穿过病变部位并进入脊髓的尾部。突触素表达与BDA阳性轴突和损伤部位远端的神经元共定位。发现移植的细胞会迁移到病变中,但不会沿着轴突生长的路径散布。移植后,细胞分化为星形胶质细胞或少突胶质细胞,但不分化为神经元。此外,与NSC移植组相比,NSC介质的给药并不限制受损大鼠的轴突发芽和功能恢复。结论人类胚胎神经干细胞可以促进大鼠脊髓损伤后功能性皮质脊髓轴突的再生和突触的重建。作用主要是通过干细胞对脊髓的营养作用。

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