基础医学与临床 ›› 2013, Vol. 33 ›› Issue (2): 199-204.

• 研究论文 • 上一篇    下一篇

JNK信号通路介导高糖诱导的大鼠心肌成纤维细胞增殖

刘丽华1,房彩霞1,邓永贵2,周红1   

  1. 1. 河北医科大学第二医院
    2. 河北医科大学第二医院内分泌科 石家庄
  • 收稿日期:2012-09-05 修回日期:2012-12-19 出版日期:2013-02-05 发布日期:2013-01-25
  • 通讯作者: 周红 E-mail:zhoubs2008@yahoo.cn

c-Jun N-terminal kinase pathway mediates high glucose-induced proliferation of cardiac fibroblasts in rats

  • Received:2012-09-05 Revised:2012-12-19 Online:2013-02-05 Published:2013-01-25

摘要: 目的 明确c-Jun氨基末端激酶(JNK)信号通路在高糖诱导大鼠心肌成纤维细胞增殖中的作用。方法 提取大鼠原代心肌成纤维细胞,观察不同糖浓度(12、18和25 mmol/L葡萄糖)和不同刺激时间(0、12、24和48 h)对JNK通路的影响。实验分为对照组(5.5 mmol/L葡萄糖)、高糖组(25 mmol/L葡萄糖)、JNK抑制剂SP600125组(25 mmol/L葡萄糖+SP600125 10、20 μmol/L)和高渗组(5.5 mmol/L葡萄糖+19.5 mmol/L甘露醇)培养48 h,应用MTT测定细胞增殖、Weastern blot测定JNK磷酸化水平和增殖细胞核抗原(PCNA)的蛋白表达、RT-PCR检测c-jun基因表达。结果 高糖呈时间和剂量依赖性增加JNK磷酸化水平。与对照组比较,高糖显著地促进了心肌成纤维细胞的增殖(0.44±0.02 vs 0.31±0.02, P<0.01),并上调了c-jun的基因表达和PCNA蛋白水平。 SP600125能够浓度依赖性地抑制高糖诱导的细胞增殖和JNK通路的激活。结论 JNK信号通路部分地介导了高糖诱导的大鼠心肌成纤维细胞增殖。

关键词: 【关键词】葡萄糖, 心肌成纤维细胞, 增殖, c-jun氨基末端激酶

Abstract: Objective To determine whether JNK signaling pathway is involved in high glucose (HG)-induced proliferation of cardiac fibroblasts (CFs) in rats. Methods Rat CFs were cultured in DMEM (NG: 5.5 mmol/L D-glucose; HG: 12, 18, 25 mmol/L D-glucose; OSM: 5.5 mmol/L D-glucose + 19.5 mmol/L mannitol) for indicated time periods (0, 12, 24, 48 h). Meanwhile, Rat CFs were cultured in DMEM (25 mmol/L D-glucose) with SP600125 (10, 20 μmol/L), a JNK inhibitor, for 48 h. Proliferation was measured by MTT. The expression of proliferating cell nuclear antigen (PCNA), total JNK and phosphorylation of JNK were detected by Western blot analysis. c-jun mRNA expression was assessed by RT-PCR. Results Treatment of CFs with HG significantly increased phosphorylation of JNK in time- and glucose concentration-dependent manner. Compared with NG group, exposure of CFs to HG (25 mmol/L) significantly promoted the proliferation of CFs (0.44±0.02 vs 0.31±0.02, P<0.01), and upregulated c-jun mRNA expression and PCNA levels. SP600125 significantly suppressed HG-induced the proliferation of CFs and the activity of JNK in a dose-dependent manner. Conclusions HG stimulates the proliferation of CFs partially through JNK pathway activation.

Key words: Keywords: glucose, cardiac fibroblasts, proliferation, c-jun N-terminal kinase pathway