基础医学与临床 ›› 2012, Vol. 32 ›› Issue (8): 906-910.

• 研究论文 • 上一篇    下一篇

Ang-(1-7)与Mas结合促进NIT细胞分泌胰岛素

张雪莲1,杨金奎1,尚军2,王阳1   

  1. 1. 首都医科大学附属北京同仁医院
    2. 北京同仁医院
  • 收稿日期:2011-12-23 修回日期:2012-05-08 出版日期:2012-08-05 发布日期:2012-07-17
  • 通讯作者: 杨金奎 E-mail:yangjk@trhos.com
  • 基金资助:
    骨髓间充质干细胞瘤化中STAT3信号通路过度激活的作用机制与规避研究

The binding of Ang-(1-7) and Mas stimulates insulin secretion in NIT cell

  • Received:2011-12-23 Revised:2012-05-08 Online:2012-08-05 Published:2012-07-17

摘要: 目的 体外研究Ang-(1-7)对NIT细胞胰岛素分泌的影响及其潜在机制。方法 将NIT细胞在不同浓度Ang-(1-7)(10-8 mol/L~10-3mol/L)培养24 h,ELISA法检测NIT细胞对葡萄糖刺激的胰岛素分泌功能。用RT-PCR法,从NIT细胞中扩增Mas、GLUT-2和TGF-β1基因的全长cDNA 序列。将NIT细胞在10-5 mol/L Ang-(1-7)条件下培养48h,QRT-PCR方法检测NIT细胞Mas、GLUT-2及TGF-β1的mRNA表达,Western印迹方法测定NIT细胞Mas、GLUT-2及TGF-β1的蛋白表达。结果 NIT细胞系随着细胞外Ang-(1-7)浓度(10-8 mol/L~10-3 mol/L)的增加胰岛素分泌增加,10-5mol/L Ang-(1-7)组胰岛素分泌量为8.86±0.53 mIU/L,显著高于对照组(8.06±0.39 mIU/L)(P<0.05)。与对照组相比,经10-5mol/L Ang-(1-7)预处理的NIT细胞Mas及GLUT-2的mRNA和蛋白表达上调(P<0.05~0.01);相反,经10-5mol/L Ang-(1-7)预处理的NIT细胞TGF-β1的mRNA和蛋白表达水平下降(P<0.05)。结论 Ang-(1-7) 与Mas 结合能够促进NIT细胞分泌胰岛素,这可能与提高NIT细胞摄取葡萄糖的能力、抑制纤维化进程等相关。

关键词: 肾素血管紧张素系统,血管紧张素转换酶2, 血管紧张素(1-7),Mas

Abstract: Objective To investigate the effects of Ang-(1-7) and Mas receptor on insulin secretion in NIT cell and their potential mechanism. Methods NIT cells were exposed to Ang-(1-7) of different concentrations (10-8 mol/l~10-3mol/l) for 24 hours. Glucose stimulated insulin secretion by NIT cells was detected with ELISA. The full cDNA sequence of Mas, GLUT-2 and TGF-β1 were obtained from NIT cell line using RT-PCR. After NIT cells were exposed to 10-5mol/l Ang-(1-7) for 48 hours, Mas, GLUT-2 and TGF-β 1 mRNA expression were estimated by real-time PCR; Meantime, the protein levels of the afore variables were detected by Western blotting analysis. Results NIT islet cell line responds to extracellular Ang-(1-7) (10-8 mol/l -10-3mol/l) with increased insulin secretion in a concentration dependent manner. The insulin secretion increased significantly in the presence of 10?5mol/l Ang-(1-7) (8.86±0.53 mIU/l) compared to control group (8.06±0.39 mIU/l) (P<0.05). In the experiments, compared to control group, the cells preincubated with 10?5mol/l Ang-(1-7) were up-regulated in Mas gene and protein expression (P<0.05~0.01), and caused a significant stimulation of mRNA and protein expression of GLUT-2 (P<0.05). On the contrary, the result showed a reduction in TGF-β1 mRNA and protein expression (P<0.05). Conclusion The binding of Ang-(1-7) and Mas can stimulate the NIT cells to secrete insulin, probably due to its enhancing the ability to intake glucose and inhibit the progression of fibrosis.

Key words: Rennin-angiotensin system, Angiotensin-converting Enzyme 2, Angiotensin-(1-7), Mas

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