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Stable transfection into rat bone marrow mesenchymal stem cells by lentivirus-mediated NT-3

机译:慢病毒介导的NT-3稳定转染大鼠骨髓间充质干细胞

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摘要

Transplantation of bone marrow mesenchymal stem cells (BMSCs) is the most promising therapeutic strategy in the treatment of spinal cord injuries. BMSCs have a wide variety of sources and are characterized by being exempt from immune rejection, marked secretory functions and neuronal plasticity during differentiation. The lentiviral vector, namely PLV.Ex3d.Peo-EF1A-NT3-internal ribosome entry site-enhanced green fluorescent protein, was constructed and subsequently transfected into Sprague Dawley (SD) rat BMSCs. The gene and protein expression levels of the nucleic acid neurotrophin-3 (NT-3) were then detected. The results demonstrated that the constructed NT-3 gene lentiviral expression vector matched the expected design and that the NT-3 gene was transfected into the BMSCs via the lentivirus-mediated method at a transfection efficiency of 60-70%. NT-3 gene expression was detected within the stably transfected positive cells at the nucleic acid and protein levels. The cell morphology and biological activity of BMSCs did not alter significantly following transfection with NT-3. NT-3-transfected SD BMSCs were successfully constructed and served as effective vector seed cells with stable expression. These results can be used as a reference for subsequent studies on the transplantation therapy of rat spinal cord injuries using lentivirus-mediated NT-3-transfected SD BMSCs.
机译:骨髓间充质干细胞(BMSC)的移植是治疗脊髓损伤中最有希望的治疗策略。骨髓间充质干细胞来源广泛,其特征是在分化过程中免于免疫排斥,明显的分泌功能和神经元可塑性。构建慢病毒载体,即PLV.Ex3d.P / neo-EF1A-NT3-内部核糖体进入位点增强的绿色荧光蛋白,然后将其转染到Sprague Dawley(SD)大鼠BMSCs中。然后检测核酸神经营养蛋白3(NT-3)的基因和蛋白质表达水平。结果表明,所构建的NT-3基因慢病毒表达载体符合预期设计,并且通过慢病毒介导的方法以60-70%的转染效率将NT-3基因转染到BMSC中。在核酸和蛋白质水平上稳定转染的阳性细胞中检测到NT-3基因表达。 NT-3转染后,BMSCs的细胞形态和生物学活性没有明显改变。成功构建了NT-3转染的SD BMSC,并用作稳定表达的有效载体种子细胞。这些结果可作为后续研究慢病毒介导的NT-3转染的SD BMSCs对大鼠脊髓损伤的移植治疗的参考。

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