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Insulin producing cell clusters derived from very small embryonic like stem cells are potent to treat diabetics mice

机译:源自非常小的胚胎样干细胞的产生胰岛素的细胞簇有效治疗糖尿病小鼠

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Considerable effort has been expended to isolate stem cells from a number of different tissues to use in regenerative medicine. In this study, we purposed to reckon up the ability of mouse very small embryonic like stem cells (VSEL) differentiation into insulin producing cell clusters(IPCCs), in order to treatment of diabetes. Mouse Bone marrow VSEL stem cells, isolated with Fluorescent activating cell sorting (FACS) method by using Fluorescent antibodies against CD45, CXCR4 and Sca1markers. After differentiation of VSEL stem cells into IPCCs with Activin A and nicotinamide as main factors of differentiation, RT-PCR and immunocytochemistry revealed that newly IPCCs could express Ins1, Ins2, PDX1 and Glut2. Invitro insulin secretion by IPCCs was confirmed by ELISA kit. For treatment, we injected IPCCs into thigh muscle of diabetic mice. Results showed that newly derived IPCCs were capable to produce insulin in vivo. There was a significant decrease in mean blood sugar of diabetic mice after passing 3 weeks from cell therapy. This study provides a strategy for using autologous VSEL stem cells for curing diabetes and other regenerative disease, as an alternative for other stem cell types.
机译:已经花费了相当大的努力从许多不同的组织中分离干细胞以用于再生医学。在这项研究中,我们旨在计算小鼠非常小的胚胎样干细胞(VSEL)分化为产生胰岛素的细胞簇(IPCC)的能力,以治疗糖尿病。使用针对CD45,CXCR4和Sca1标记的荧光抗体,通过荧光激活细胞分选(FACS)方法分离的小鼠骨髓VSEL干细胞。在以激活素A和烟酰胺为主要分化因子将VSEL干细胞分化为IPCC后,RT-PCR和免疫细胞化学表明,新的IPCC可以表达Ins1,Ins2,PDX1和Glut2。通过ELISA试剂盒证实了IPCC的体外胰岛素分泌。为了治疗,我们将IPCC注射到糖尿病小鼠的大腿肌肉中。结果表明,新衍生的IPCC能够在体内产生胰岛素。细胞疗法治疗3周后,糖尿病小鼠的平均血糖显着降低。这项研究提供了使用自体VSEL干细胞治疗糖尿病和其他再生疾病的策略,作为其他干细胞类型的替代方法。

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