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作 者:刘丽华[1] 房彩霞[1] 邓永贵[1] 周红[1]
机构地区:[1]河北医科大学第二医院内分泌科,河北石家庄050000
出 处:《基础医学与临床》2013年第2期199-204,共6页Basic and Clinical Medicine
基 金:河北省卫生厅重大课题资助项目(20090007)
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、20μmol/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。Objective To determine whether JNK signaling pathway is involved in high glucose (HG) -induced pro- liferation 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 in- dicated 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. 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. Conclusion HG stimulatesthe proliferation of CFs partially through JNK pathway activation.
关 键 词:葡萄糖 心肌成纤维细胞 增殖 C-JUN氨基末端激酶
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