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首页> 外文期刊>Neural regeneration research >Effect of stromal cell-derived factor-1/CXCR4 axis in neural stem cell transplantation for Parkinson’s disease
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Effect of stromal cell-derived factor-1/CXCR4 axis in neural stem cell transplantation for Parkinson’s disease

机译:基质细胞衍生因子-1 / CXCR4轴在帕金森病中神经干细胞移植中的影响

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Previous studies have shown that neural stem cell transplantation has the potential to treat Parkinson’s disease, but its specific mechanism of action is still unclear. Stromal cell-derived factor-1 and its receptor, chemokine receptor 4 (CXCR4), are important regulators of cell migration. We speculated that the CXCR4/stromal cell-derived factor 1 axis may be involved in the therapeutic effect of neural stem cell transplantation in the treatment of Parkinson’s disease. A Parkinson’s disease rat model was injected with 6-hydroxydopamine via the right ascending nigrostriatal dopaminergic pathway, and then treated with 5 μL of neural stem cell suspension (1.5 × 10 4 /L) in the right substantia nigra. Rats were intraperitoneally injected once daily for 3 days with 1.25 mL/kg of the CXCR4 antagonist AMD3100 to observe changes after neural stem cell transplantation. Parkinson-like behavior in rats was detected using apomorphine-induced rotation. Immunofluorescence staining was used to determine the immunoreactivity of tyrosine hydroxylase, CXCR4, and stromal cell-derived factor-1 in the brain. Using quantitative real-time polymerase chain reaction, the mRNA expression of stromal cell-derived factor-1 and CXCR4 in the right substantia nigra were measured. In addition, western blot assays were performed to analyze the protein expression of stromal cell-derived factor-1 and CXCR4. Our results demonstrated that neural stem cell transplantation noticeably reduced apomorphine-induced rotation, increased the mRNA and protein expression of stromal cell-derived factor-1 and CXCR4 in the right substantia nigra, and enhanced the immunoreactivity of tyrosine hydroxylase, CXCR4, and stromal cell-derived factor-1 in the brain. Injection of AMD3100 inhibited the aforementioned effects. These findings suggest that the stromal cell-derived factor-1/CXCR4 axis may play a significant role in the therapeutic effect of neural stem cell transplantation in a rat model of Parkinson’s disease. This study was approved by the Animal Care and Use Committee of Kunming Medical University, China (approval No. SYXKK2015-0002) on April 1, 2014.
机译:以前的研究表明,神经干细胞移植有可能治疗帕金森病的潜力,但其特定的作用机制仍然尚不清楚。基质细胞衍生因子-1及其受体,趋化因子受体4(CXCR4)是细胞迁移的重要调节因子。我们推测CXCR4 /基质细胞衍生的因子1轴可以参与神经干细胞移植治疗帕金森病治疗的治疗效果。通过右上行的纽粒子多巴胺能途径,用6-羟基多胺注射帕金森病大鼠模型,然后用5μl的神经干细胞悬浮液(1.5×10 4 / L)在正确的真实性内部。每天一次腹膜内注射一次3天,用1.25ml / kg CXCR4拮抗剂AMD3100进行3天,以观察神经干细胞移植后的变化。使用Abomorphine诱导的旋转检测大鼠帕金森的行为。使用免疫荧光染色来确定酪氨酸羟化酶,CXCR4和基质细胞衍生因子-1的免疫反应性。使用定量实时聚合酶链反应,测定了合理细胞衍生的因子-1和右实质性NIGRA中的CXCR4的mRNA表达。此外,进行蛋白质印迹测定以分析基质细胞衍生因子-1和CXCR4的蛋白质表达。我们的结果表明,神经干细胞移植显着降低了邻梅啡诱导的旋转,增加了基质细胞衍生因子-1和CXCR4在正确的真实性NIGRA中的mRNA和蛋白表达,并增强了酪氨酸羟化酶,CXCR4和基质细胞的免疫反应性大脑中的重点 - 1。注射AMD3100抑制上述效果。这些发现表明,基质细胞衍生的因子-1 / CXCR4轴可能在神经干细胞移植在帕金森病的大鼠模型中的治疗作用中起重要作用。 2014年4月1日,本研究经昆明医科大学的动物护理和用途委员会批准(批准号SYXKK215-0002)。

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