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骨髓间充质干细胞与小鼠胰腺β细胞的共微囊化用于提高I型糖尿病治疗效果

Co-microencapsulation of BMSCs and mouse pancreatic β cells for improving the efficacy of type I diabetes therapy.

作者信息

Long Ruimin, Liu Yuangang, Wang Shibin, Ye Li, He Peng

机构信息

College of Chemical Engineering, Huaqiao University, Xiamen - China.

Fujian Provincial Key Laboratory of Biochemical Technology, Huaqiao University, Xiamen - China.

出版信息

Int J Artif Organs. 2017 May 9;40(4):169-175. doi: 10.5301/ijao.5000555. Epub 2017 Mar 21.

DOI:10.5301/ijao.5000555
PMID:28362046
Abstract

INTRODUCTION

To overcome the shortcomings of pancreas transplantation and insulin injection treatment for type I diabetes, biocompatible materials were used to prepare alginate-chitosan-alginate microcapsules that co-encapsulated bone marrow mesenchymal stem cells and mouse pancreatic β cells to treat diabetic mice.

METHODS

Blank alginate-chitosan-alginate (ACA) microcapsules and co-microencapsulated cells were prepared using a high-voltage electrostatic method and then characterized using an inverted microscope. Cell viability was evaluated using AO/EB staining. ELISA kit was used to detect insulin secretion. Peri-orbital blood samples were obtained from the mice for blood glucose determination every week for one month.

RESULTS

After 28 days of in vitro culture, the secretion of insulin following co-microencapsulation was higher than that observed for microencapsulated beta-TC-6 cells alone. On the 28th day after transplantation, the blood glucose level was 6.86 mmol/L in the microencapsulated beta-TC-6 group. On the 14th day, the blood glucose level was 6.80 mmol/L in the co-microencapsulated BMSC/beta-TC-6 group, which was close to the normal blood glucose level of healthy mice. These results indicated that the efficacy in reducing blood glucose was better in the co-microencapsulated BMSC/beta-TC-6 group.

CONCLUSIONS

This primary study indicated that combining microencapsulation technology and co-culture of stem cells and somatic cells shows promise for the treatment of type I diabetes mellitus.

摘要

引言

为克服胰腺移植和胰岛素注射治疗I型糖尿病的缺点,采用生物相容性材料制备了共包封骨髓间充质干细胞和小鼠胰腺β细胞的海藻酸钠-壳聚糖-海藻酸钠微胶囊,用于治疗糖尿病小鼠。

方法

采用高压静电法制备空白海藻酸钠-壳聚糖-海藻酸钠(ACA)微胶囊和共微包封细胞,然后用倒置显微镜进行表征。采用AO/EB染色评估细胞活力。用ELISA试剂盒检测胰岛素分泌。每周从小鼠眼眶周围采集血样,持续一个月以测定血糖。

结果

体外培养28天后,共微包封后的胰岛素分泌高于单独微包封β-TC-6细胞的情况。移植后第28天,微包封β-TC-6组的血糖水平为6.86 mmol/L。在第14天,共微包封BMSC/β-TC-6组的血糖水平为6.80 mmol/L,接近健康小鼠的正常血糖水平。这些结果表明,共微包封BMSC/β-TC-6组在降低血糖方面的效果更好。

结论

这项初步研究表明,将微包封技术与干细胞和体细胞共培养相结合在治疗I型糖尿病方面具有前景。

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