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Gene Expression Pattern of Insulin-Like Growth Factor-I Receptor on Mesenchymal Stem Cells Induced by Tumor Necrosis Factor-a

机译:肿瘤坏死因子-α诱导间充质干细胞表达胰岛素样生长因子-I受体的基因表达模式

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Cell-based therapy has been implicated in treatment in a wide range of diseases. Mesenchymal stem cells from various sources such as bone marrow are available. These cells are one of the major candidates in cell therapy. The production of insulin-like growth factor-I increases in the regenerating organ. The insulin-like growth factor-I in liver regeneration is effective after binding to insulin-like growth factor-I receptor. We hypothesized that tumor necrosis factor- stimulate mesenchymal stem cells to cause insulin-like growth factor-I receptor expression. Bone marrow was aspirated from human normal donor after informing consent. Cells were isolated and cultured. Identification of cells with flow cytometric analysis and functional tests were performed. Fourth passage cells were treated with tumor necrosis factor- at different doses (1 ng/mL and 10 ng/mL) and incubated at different times (2, 10, 24 and 48 hours). Insulin-like growth factor-I receptor gene expression was investigated using real time-polymerase chain reaction technique. Flow cytometric analysis showed that the human bone marrow mesenchymal stem cells were positive for CD90 and negative for CD45 and CD80. The insulin-like growth factor-I receptor gene expression was increased in tumor necrosis factor- treated in comparison with untreated cells. Increase gene expression pattern of insulin-like growth factor-I receptor in human bone marrow derived mesenchymal stem cells may be used for clinical stem cell therapy in acute liver failure.
机译:基于细胞的疗法已经涉及多种疾病的治疗。可利用来自各种来源的间充质干细胞,例如骨髓。这些细胞是细胞疗法中的主要候选药物之一。胰岛素样生长因子-1的产生在再生器官中增加。与胰岛素样生长因子-1受体结合后,肝脏再生中的胰岛素样生长因子-1有效。我们假设肿瘤坏死因子刺激间充质干细胞引起胰岛素样生长因子-I受体表达。知情同意后,从人类正常供体中吸出骨髓。分离细胞并培养。用流式细胞术分析和功能测试鉴定细胞。第四代细胞用不同剂量(1 ng / mL和10 ng / mL)的肿瘤坏死因子处理,并在不同时间(2、10、24和48小时)孵育。使用实时聚合酶链反应技术研究了胰岛素样生长因子-I受体基因的表达。流式细胞仪分析显示,人骨髓间充质干细胞CD90阳性,CD45和CD80阴性。与未处理的细胞相比,在用肿瘤坏死因子处理的胰岛素样生长因子-1受体基因表达增加。人骨髓来源的间充质干细胞中胰岛素样生长因子-I受体基因表达模式的增加可用于急性肝衰竭的临床干细胞治疗。

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