朱晗玉, 洪权, 张冬, 耿文佳, 刘沫言, 谢院生, 陈香美. 单核细胞趋化蛋白-1通过促进胰淀素表达调控胰岛β细胞凋亡[J]. 解放军医学院学报, 2012, 33(5): 489-491,499. DOI: CNKI:11-3275/R.20111123.0839.001
引用本文: 朱晗玉, 洪权, 张冬, 耿文佳, 刘沫言, 谢院生, 陈香美. 单核细胞趋化蛋白-1通过促进胰淀素表达调控胰岛β细胞凋亡[J]. 解放军医学院学报, 2012, 33(5): 489-491,499. DOI: CNKI:11-3275/R.20111123.0839.001
ZHU Han-yu, HONG Quan, ZHANG Dong, GENG Wen-jia, LIU Mo-yan, XIE Yuan-sheng, CHEN Xiang-mei. Monocyte chemoattractant protein-1 regulates apoptosis of islet β-cells by promoting expression of amylin[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2012, 33(5): 489-491,499. DOI: CNKI:11-3275/R.20111123.0839.001
Citation: ZHU Han-yu, HONG Quan, ZHANG Dong, GENG Wen-jia, LIU Mo-yan, XIE Yuan-sheng, CHEN Xiang-mei. Monocyte chemoattractant protein-1 regulates apoptosis of islet β-cells by promoting expression of amylin[J]. ACADEMIC JOURNAL OF CHINESE PLA MEDICAL SCHOOL, 2012, 33(5): 489-491,499. DOI: CNKI:11-3275/R.20111123.0839.001

单核细胞趋化蛋白-1通过促进胰淀素表达调控胰岛β细胞凋亡

Monocyte chemoattractant protein-1 regulates apoptosis of islet β-cells by promoting expression of amylin

  • 摘要: 目的 观察单核细胞趋化蛋白-1(MCP-1)对胰岛β细胞凋亡的影响,并探讨其可能机制。 方法 体外培养大鼠胰岛β细胞株INS-1E,给予1ng/ml的MCP-1刺激48h后,real-time PCR及western blot检测细胞中Amylin的mRNA及蛋白表达水平,同时流式细胞仪检测细胞凋亡情况。细胞转染Amylin SiRNA,再给予MCP-1刺激,同样采用流式细胞仪技术检测细胞凋亡情况。 结果 INS-1E细胞经MCP-1刺激后,细胞中Amylin的mRNA及蛋白表达水平均升高(P<0.05),细胞出现了凋亡现象。而预先转染了抑制Amylin表达的siRNA后再进行MCP-1的刺激,此时细胞的凋亡率低于单独刺激组(P<0.05)。 结论 MCP-1通过促进胰淀素的表达调控胰岛β细胞的凋亡,从而影响血糖代谢。

     

    Abstract: Objective To observe the effect of monocyte chemoattractant protein-1(MCP-1) on apoptosis of pancreatic β-cells and study its possible mechanism. Methods Forty-eight hours after in vitro cultured rat pancreatic β cell line INS-1E was stimulated with 1ng/ml MCP-1,expression levels of amylin mRNA and protein in rat pancreatic β cells were measured by real-time PCR and Western blot,respectively.Apoptosis of rat pancreatic β cells was detected by flow cytometry.Forty-eight hours after in vitro cultured rat pancreatic β cells transfected with amylin SiRNA were stimulated again with 1ng/ml MCP-1,their apoptosis was detected by flow cytometry. Results The expression levels of amylin mRNA and protein in INS-1E cells were significantly higher after MCP-1 stimulation than before MCP-1 stimulation(P<0.05) and the apoptosis of INS-1E cells occurred.However,the apoptosis rate of INS-1E cells was lower when the expression level of amylin mRNA in INS-1E cells was stimulated with MCP-1 and transfected with amylin mRNA than when the expression level of amylin mRNA in INS-1E cells was only stimulated with MCP-1(P<0.05). Conclusion MCP-1 can regulate the apoptosis of rat pancreatic β cells by promoting the expression of amylin,thus influencing the metabolism blood sugar.

     

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