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Exendin-4对游离脂肪酸诱导肝细胞sirt6表达及其对糖异生作用的影响
引用本文:肖元元,王倩倩,毛月芹,魏美林,韩峻峰,殷峻,魏丽.Exendin-4对游离脂肪酸诱导肝细胞sirt6表达及其对糖异生作用的影响[J].医学研究杂志,2015,44(1):39-43.
作者姓名:肖元元  王倩倩  毛月芹  魏美林  韩峻峰  殷峻  魏丽
作者单位:200233,上海交通大学附属第六人民医院内分泌代谢科、上海市糖尿病临床医学中心、上海市糖尿病重点实验室、上海市糖尿病研究所、上海市代谢病临床医学中心
基金项目:国家自然科学基金资助项目 (81370956);上海交通大学专项基金资助项目 (2011JDZX021)
摘    要:目的观察Exendin-4对游离脂肪酸诱导的肝细胞sirt6表达的影响及其在肝脏糖异生过程中的调控作用。方法体外培养人肝癌细胞株Hep G2细胞,根据干预措施分为正常对照组、Exendin-4(100nmol/L)处理组、游离脂肪酸对待组、游离脂肪酸+Exendin-4处理组。Western blot法检测各组细胞中sirt6表达的变化。以stealth siRNA干扰Hep G2细胞中sirt6的表达后给予相同处理,Western blot法检测sirt6表达蛋白水平的变化,RT-PCR检测sirt6及糖异生相关基因G6Pase和PEPCK mRNA水平的变化。结果与正常对照组相比游离脂肪酸可显著降低肝细胞内sirt6蛋白的表达,而经Exendin-4处理后,sirt6表达显著升高。与正常对照组相比,游离脂肪酸可诱导肝细胞糖异生相关基因表达的升高,经过Exendin-4处理后,可相应降低上述基因的表达。当下调sirt6表达后,则抑制了由Exendin-4对改善游离脂肪酸诱导肝细胞糖异生相关基因的调节作用。结论游离脂肪酸可降低肝细胞sirt6的表达,Exendin-4可改善由游离脂肪酸诱导的肝细胞sirt6表达的下降及糖异生相关基因表达的升高;Exendin-4可能是通过对sirt6的调节从而在肝脏糖异生过程中发挥重要作用的。

关 键 词:胰高血糖素样肽-1  糖异生  脂肪肝
收稿时间:2014/5/17 0:00:00
修稿时间:2014/5/30 0:00:00

Effect of Exendin-4 on the Expression of Sirt6 and Hepatic Gluconeogenesis in the Free Fatty Acid-induced HepG2 Cell
Xiao Yuanyuan,Wang Qianqian,Mao Yueqin.Effect of Exendin-4 on the Expression of Sirt6 and Hepatic Gluconeogenesis in the Free Fatty Acid-induced HepG2 Cell[J].Journal of Medical Research,2015,44(1):39-43.
Authors:Xiao Yuanyuan  Wang Qianqian  Mao Yueqin
Institution:Department of Endocrinology and Metabolism, Shanghai Jiaotong University Affiliated Sixth People's Hospital, Shanghai Clinical Center for Diabetes, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai Diabetes Institute, Shanghai Clinical Center for Metabolic Diseases, Shanghai 200233, China;Department of Endocrinology and Metabolism, Shanghai Jiaotong University Affiliated Sixth People's Hospital, Shanghai Clinical Center for Diabetes, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai Diabetes Institute, Shanghai Clinical Center for Metabolic Diseases, Shanghai 200233, China;Department of Endocrinology and Metabolism, Shanghai Jiaotong University Affiliated Sixth People's Hospital, Shanghai Clinical Center for Diabetes, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai Diabetes Institute, Shanghai Clinical Center for Metabolic Diseases, Shanghai 200233, China;Department of Endocrinology and Metabolism, Shanghai Jiaotong University Affiliated Sixth People's Hospital, Shanghai Clinical Center for Diabetes, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai Diabetes Institute, Shanghai Clinical Center for Metabolic Diseases, Shanghai 200233, China;Department of Endocrinology and Metabolism, Shanghai Jiaotong University Affiliated Sixth People's Hospital, Shanghai Clinical Center for Diabetes, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai Diabetes Institute, Shanghai Clinical Center for Metabolic Diseases, Shanghai 200233, China;Department of Endocrinology and Metabolism, Shanghai Jiaotong University Affiliated Sixth People's Hospital, Shanghai Clinical Center for Diabetes, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai Diabetes Institute, Shanghai Clinical Center for Metabolic Diseases, Shanghai 200233, China;Department of Endocrinology and Metabolism, Shanghai Jiaotong University Affiliated Sixth People's Hospital, Shanghai Clinical Center for Diabetes, Shanghai Key Laboratory of Diabetes Mellitus, Shanghai Diabetes Institute, Shanghai Clinical Center for Metabolic Diseases, Shanghai 200233, China
Abstract:Objective To examine the influence of Exendin-4 on the experssion of sirt6 and other related gluconeogenesis genes in fatty liver cell culture model. Methods HepG2 cells were randomly divided into 4 groups: normal control group, Exendin-4(100nmol/L) treated group, FFA treated group, FFA+Exendin-4(100nmol/L) treated group.Western blot was used to detect the expression of sirt6. Stealth siRNA was used to inhibit the expression of sirt6.After the treatment,the mRNA of Sirt6 and hepatic gluconeogenesis gene G6Pase,PEPCK were detected by RT-PCR. Results Compared with the control group,the sirt6 protein expression level was decreased in FFA-stimulated HepG2 cells.However, 100nmol/L Exendin-4 treatment could improve the FFA-decreased the expression of sirt6. Exendin-4 treatment significantly reduced the mRNA level of G6Pase and PEPCK induced by the FFAs. However, when down-regulated the expression of sirt6 by siRNA, the effects of Exendin-4 on the hepatic gluconeogenic improvement had been diminished. Conclusion FFAs could decrease the expression of sirt6 in HepG2 cells. Exendin-4 reverse the down-regulation of sirt6 induced by the FFAs.Exendin-4 treatment may attenuate and improve hepatic gluconeogenesis in liver tissues through the activation of sirt6 signaling cascade.
Keywords:Glucagon-like peptide-1  Gluconeogenesis  NAFLD
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