›› 2010, Vol. 9 ›› Issue (1): 37-40.

• 基础研究 • 上一篇    下一篇

蛋白激酶C对高糖作用下腹膜间皮细胞葡萄糖转运蛋白1调节作用

丁 红 马健飞 樊 怡   

  1. 中国医科大学附属第一医院肾内科
  • 收稿日期:2009-05-05 修回日期:1900-01-01 出版日期:2010-01-12 发布日期:2010-01-12
  • 通讯作者: 马健飞

PKC's effect on glucose transporter 1 with high glucose in peritoneal mesothelial cells

DING Hong, MA Jian-fei, FAN Yi.   

  1. Department of Nephrology, The First affiliated Hospital, China Medical University, Shenyang 110001, China;
  • Received:2009-05-05 Revised:1900-01-01 Online:2010-01-12 Published:2010-01-12

摘要:

【摘要】目的 观察蛋白激酶C(PKC)对高糖作用下体外培养的大鼠腹膜间皮细胞(PMCs)胞膜上葡萄糖转运蛋白1(GLUT1)表达的调节,以探讨长期腹透时如何避免腹膜损伤、改善腹膜透析疗效。方法 胰酶消化法提取雄性Wistar大鼠的PMCs细胞进行培养,分别加入不同浓度葡萄糖及PKC抑制剂G?6976,间接免疫荧光法检测PMCs上GLUT1表达,流式细胞仪检测作用前后细胞膜上GLUT1量的改变,生化分析仪检测培养液内葡萄糖浓度的变化。结果 高糖可增加细胞膜上GLUT1的表达,同时伴有PMCs对葡萄糖的转运增加(P<0.05)。G ?6976明显抑制了高糖对GLUT1的诱导,且葡萄糖的转运亦下降。 结论 葡萄糖以浓度依赖方式上调PMCs细胞膜上GLUT1的蛋白表达,同时伴有PMCs对葡萄糖转运的增加。PKC通路在其中发挥重要作用,应用PKC抑制剂可拮抗高糖对GLUT1表达的诱导作用。

关键词: 腹膜间皮细胞, 葡萄糖转运蛋白1, 蛋白激酶C

Abstract:

【Abstract】 Objective In order to avoid peritomum injury and to improve the efficiency of peritoneal dialysis during the dialysis, We investigated the regulating effect of protein kinase C(PKC)on Peritoneal Mesothelial Cells (PMCs) of the plasma membrane cultivated in high concentrations of glucoses. Methods PMCs that had been harvested from male Wistar rats by Enzymatic disaggregation method was cultivated in different concentrations glucoses. PKC inhibitor G6976 was applied to obstruct the functions of PKC. Indirect immunofluorescent staining was used for the identification of expression of GLUT1 on the plasma membrane. Flow cytomety was used for the analyses the mean fluorescence intensity (MFI) of GLUT1 on the plasma membrane. Glucose concentrations were examined by biochemistry analyzer. Results Compare with the control group High glucose can promote the expression of GLUT1 on PMCs, The glucose absorption of PMCs increase also (p<0.05), and G6976 can significantly restrain both of these two effects. Conclusion High glucose up-regulated the expressions of GLUT1 on the plasma membrane in dose-dependent manner, and the absorption of glucose in PMCs increased also. The PKC signaling pathway play an important role on it, and the inhibitor of PKC can partly block the expression of GLUT1 and the transportation of glucose.

Key words: glucose transporter1, protein kinase C

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