首页> 外文期刊>Advances in Experimental Medicine and Biology >Intravenous Infusion of Human Adipose Tissue-Derived Mesenchymal Stem Cells to Treat Type 1 Diabetic Mellitus in Mice: An Evaluation of Grafted Cell Doses
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Intravenous Infusion of Human Adipose Tissue-Derived Mesenchymal Stem Cells to Treat Type 1 Diabetic Mellitus in Mice: An Evaluation of Grafted Cell Doses

机译:静脉输注人脂肪组织衍生的间充质干细胞治疗小鼠中的1型糖尿病患者:对接枝细胞剂量的评估

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摘要

Mesenchymal stem cell (MSC) transplantation is a novel treatment for diabetes mellitus, especially type 1 diabetes. Many recent publications have demonstrated the efficacy of MSC transplantation on reducing blood glucose and increasing insulin production in both preclinical and clinical trials. However, the investigation of grafted cell doses has been lacking. Therefore, this study aimed to evaluate the different doses of MSCs on treatment of type 1 diabetes in mouse models. MSCs were isolated and expanded from human adipose tissue. Streptozotocin (STZ)-induced diabetic mice were divided into two groups that were intravenously transfused with two different doses of human MSCs: 10(6) or 2.10(6) cells/mouse. After transplantation, both grafted and placebo mice were monitored weekly for their blood glucose levels, glucose and insulin tolerance, pancreatic structural changes, and insulin production for 56 days after transplantation. The results showed that the higher dose of MSCs (2.10(6) cells/mouse) remarkably reduced death rate. The death rates were 50%, 66%, and 0% in placebo group, low-dose (1.10(6) MSCs) group, and high-dose (2.10(6) MSCs) group, respectively, after 56 days of treatment. Moreover, blood glucose levels were lower for the high-dose group compared to other groups. Glucose and insulin tolerance, as well as insulin production, were significantly improved in mice transplanted with 2.10(6) cells. The histochemical analyses also support these results. Thus, a higher (e.g., 2.10(6)) dose of MSCs may be an effective dose for treatment of type 1 diabetes mellitus.
机译:间充质干细胞(MSC)移植是糖尿病的新型治疗,尤其是1型糖尿病。最近的许多出版物表明了MSC移植对降低血糖和临床前试验中胰岛素产生的疗效。然而,缺乏对接枝细胞剂量的调查。因此,本研究旨在评估小鼠模型中1型糖尿病的不同剂量的MSCs。将MSCs分离并从人脂肪组织中膨胀。链脲佐菌素(STZ)诱导的糖尿病小鼠分为两组,其静脉内将其与两种不同剂量的人MSCs:10(6)或2.10(6)个细胞/小鼠一起用。移植后,每周嫁接和安慰剂小鼠监测血糖水平,葡萄糖和胰岛素耐受性,胰腺结构变化和移植后56天的胰岛素产生。结果表明,较高剂量的MSC(2.10(6)个细胞/小鼠)显着降低了死亡率。安慰剂组的死亡率为50%,66%和0%,低剂量(1.10(6)个MSCs)组和高剂量(2.10(6)个MSCs)组分别在56天的处理后。此外,与其他基团相比,高剂量组血糖水平较低。葡萄糖和胰岛素耐受以及胰岛素产生的小鼠在移植的小鼠中显着改善2.10(6)个细胞。组织化学分析也支持这些结果。因此,更高的(例如,2.10(6))剂量的MSCs可以是用于治疗1型糖尿病的有效剂量。

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