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Transplantation of neurotrophin-3-expressing bone mesenchymal stem cells improves recovery in a rat model of spinal cord injury

机译:表达神经营养蛋白3的骨间充质干细胞的移植可改善大鼠脊髓损伤模型的恢复

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Background: This study aimed to investigate the therapeutic effects of transplanting neutrophin-3 (NT-3)-expressing bone marrow-derived mesenchymal stem cells (BMSCs) in a rat model of spinal cord injury (SCI). Methods: Forty-eight adult female Sprague-Dawley rats were randomly assigned to three groups: the control, BMSC, and NT-3-BMSC groups. BMSCs were infected with NT-3-DsRed or DsRed lentivirus and injected into the cerebrospinal fluid (CSF) via lumbar puncture (LP) 7 days after SCI in the NT-3-BMSC and BMSC groups, respectively. The hind-limb motor function of all rats was recorded using the Basso, Beattie, and Bresnahan (BBB) locomotor rating scale on days 1, 3, 7, 14, 21, 28, and 35 after transplantation. Haematoxylin-eosin (HE) staining, immunofluorescence labelling, and western blotting were performed at the final time point. Results: Expressions of NT-3, brain-derived neurotrophic factor (BDNF), and vascular endothelial growth factor (VEGF) proteins increased significantly in the NT-3-BMSC group, and hind-limb locomotor functions improved significantly in the NT-3-BMSC group compared with the other two groups. The cystic cavity area was smallest in the NT-3-BMSC group. In the NT-3-BMSC group, neurofilament 200 (NF200) and glial fibrillary acidic protein (GFAP) expression levels around the lesions were significantly increased and decreased, respectively. Conclusions: Our findings demonstrate that transplantation of NT-3 gene-modified BMSCs via LP can strengthen the therapeutic benefits of BMSC transplantation. We observed that these modified cells increased locomotor function recovery, promoted nerve regeneration, and improved the injured spinal cord microenvironment, suggesting that it could be a promising treatment for SCI.
机译:背景:这项研究旨在调查表达中性蛋白3(NT-3)的骨髓源性间充质干细胞(BMSCs)在大鼠脊髓损伤(SCI)模型中的治疗效果。方法:将48只成年雌性Sprague-Dawley大鼠随机分为三组:对照组,BMSC和NT-3-BMSC组。在NT-3-BMSC和BMSC组中,分别在SCI后7天,将BMSCs感染NT-3-DsRed或DsRed慢病毒并通过腰椎穿刺(LP)注射到脑脊液(CSF)中。在移植后第1、3、7、14、21、28和35天,使用Basso,Beattie和Bresnahan(BBB)运动评分量表记录所有大鼠的后肢运动功能。在最后一个时间点进行苏木精-伊红(HE)染色,免疫荧光标记和蛋白质印迹。结果:NT-3-BMSC组中NT-3,脑源性神经营养因子(BDNF)和血管内皮生长因子(VEGF)蛋白的表达显着增加,而NT-3组的后肢运动功能显着改善-BMSC组与其他两组相比。在NT-3-BMSC组中,胆囊腔面积最小。在NT-3-BMSC组中,病变周围的神经丝200(NF200)和胶质纤维酸性蛋白(GFAP)表达水平分别显着升高和降低。结论:我们的发现表明,经LP移植NT-3基因修饰的BMSC可以增强BMSC移植的治疗效果。我们观察到,这些修饰的细胞增加了运动功能的恢复,促进了神经的再生,并改善了受损的脊髓微环境,表明这可能是一种有希望的SCI治疗方法。

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