Suppr超能文献

利用慢病毒介导的 PDX-1 基因转导小鼠(C57BL/6)间充质干细胞体外生成葡萄糖反应性胰岛素分泌细胞。

In vitro generation of glucose-responsive insulin producing cells using lentiviral based pdx-1 gene transduction of mouse (C57BL/6) mesenchymal stem cells.

机构信息

Biochemistry Department, Pasteur Institute of Iran, Tehran, Iran.

出版信息

Biochem Biophys Res Commun. 2013 Aug 2;437(3):413-9. doi: 10.1016/j.bbrc.2013.06.092. Epub 2013 Jul 4.

Abstract

The objective of this study was to evaluate the potential of this type of recombinant lentivirus to generate glucose-responsive insulin producing cells in vitro. All steps of cloning were confirmed using restriction digests. After the transduction, mesenchymal stem cells gradually began to change their morphology and showed differentiation into islet like structures. RT-PCR results confirmed the expression of insulin1, insulin2 and pdx-1 in differentiated cells. Dithizone staining of mouse MSCs showed the concentration of glucose in islet like structures. ELISA analysis validated the insulin secretion of islet like structures which in the high-glucose medium (25mmol/l) was 7.44 fold higher than that secreted in the low-glucose medium (5mmol/l). Our results demonstrated that mouse mesenchymal stem cells can be differentiated into effective glucose-responsive insulin producing cells through our new recombinant lentiviral transduction of pdx-1 gene in vitro. This new lentiviral vector could be suggested as an effective candidate for using in gene therapy of type-1 diabetes.

摘要

本研究的目的是评估这种重组慢病毒在体外生成葡萄糖响应性胰岛素分泌细胞的潜力。克隆的所有步骤均通过酶切进行确认。转导后,间充质干细胞逐渐开始改变其形态,并表现出向胰岛样结构的分化。RT-PCR 结果证实了分化细胞中胰岛素 1、胰岛素 2 和 pdx-1 的表达。二噻嗪染色显示胰岛样结构中的葡萄糖浓度。ELISA 分析验证了胰岛样结构在高葡萄糖培养基(25mmol/L)中的胰岛素分泌量是在低葡萄糖培养基(5mmol/L)中分泌量的 7.44 倍。我们的结果表明,通过我们新的重组慢病毒转导 pdx-1 基因,可在体外将小鼠间充质干细胞分化为有效的葡萄糖响应性胰岛素分泌细胞。这种新型慢病毒载体可作为 1 型糖尿病基因治疗的有效候选物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验