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作 者:卢克良[1] 钟延美[2] 赵钧慧[1] 申志新[3] 孙吉平[4]
机构地区:[1]山东省潍坊医学院附属医院麻醉科,山东潍坊261041 [2]山东省潍坊市人民医院消化内科,山东潍坊261041 [3]山东省潍坊医学院附属医院普外科,山东潍坊261041 [4]山东省潍坊市人民医院内分泌学博士后流动站,山东潍坊261041
出 处:《中国现代普通外科进展》2009年第1期12-17,共6页Chinese Journal of Current Advances in General Surgery
摘 要:目的:研究胰腺十二指肠同源框-1(pancreatic duodenal homeobox-1,PDX-1)基因在骨髓间质干细胞(mesenchymal stem cells,MSCs)体外分化中的作用。方法:构建含有PDX-1基因的真核表达载体,转染介质Superfect介导重组载体转染MSCs,G418筛选阳性细胞后对转染组(PDX-1+MSCs)和未转染组(PDX-1-MSCs)均体外进行诱导分化,流式细胞仪检测胰岛素阳性细胞的比例,胰岛素ELISA试剂盒测定转染组诱导后细胞的胰岛素分泌功能。结果:限制性酶切分析和序列测定证实成功构建了含有PDX-1基因的真核表达载体,荧光显微镜观察证实Superfect高效介导重组载体转染MSCs;流式细胞仪发现PDX-1+MSCs分化为胰岛素分泌细胞的数量较PDX-1-MSCs明显增多(阳性率分别为28.23%±2.56%和7.08%±2.69%),25mmol高浓度葡萄糖刺激的胰岛素分泌量(115.29±2.56μU/mL)较5mmol低浓度葡萄糖刺激的分泌量明显增高(56.61±4.82μU/mL)。结论:PDX-1能增强大鼠MSCs体外分化为功能性胰岛素分泌细胞的能力,对开展胰岛移植治疗1型糖尿病有重要价值。Objective: To investigate the possible effects of pancreatic duodenal homeobox- 1 (PDX- 1)expression in transdifferentiation of bone marrow mesenchymal stem cells(MSCs)in vitro. Methods: The eukaryotic expression vector containing PDX- 1 was constructed. The vector was transfected into MSCs using Superfect, G418 was used to select the positive cells. PDX- 1 +MSCs and PDX- 1-MSCs were induced to transdifferentiat ion in vitro, the proportion of insulin- producing cells was detected by flow cytometry. Insulin secretion function of PDX- 1+MSCs was measured by ELISA. Results: Restricted enzyme analysis and sequencing showed that interest gene segment was consistent with that in Gene Bank. Recombination vector was effective transformed into MSCs demonstrated by fluorescence microscope, insulin- producing cells from PDX- 1 +MSCs were increased (28.23% ±2.56% and 7.08% ±2.69% respectively), insulin secretion of PDX- 1 +MSCs challenged by glucose in 25 mmol exceeded that in 5 mmol (115.29±2.56 μU/mL and 56.61±4.82 μU/mL respectively). Conclusion: PDX- 1 can promote adult rat MSCs to transdifferentiate into insulin- secreting cells in vitro.
关 键 词:间质干细胞 胰腺十二指肠同源框-1 干细胞移植 糖尿病 1型
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