中国免疫学杂志
中國免疫學雜誌
중국면역학잡지
CHINESE JOURNAL OF IMMUNOLOGY
2014年
11期
1477-1479,1484
,共4页
刘丹丹%俞秋霞%张慧娟%姜晓艳
劉丹丹%俞鞦霞%張慧娟%薑曉豔
류단단%유추하%장혜연%강효염
游离脂肪酸%葡萄糖转运蛋白4%G蛋白偶联受体120%胰岛素抵抗
遊離脂肪痠%葡萄糖轉運蛋白4%G蛋白偶聯受體120%胰島素牴抗
유리지방산%포도당전운단백4%G단백우련수체120%이도소저항
Free fatty acids%Glucose transporter 4%G-protein coupled receptor 120%Insulin resistance
目的:研究在3T3-L1细胞中G蛋白偶联受体120(GPR120)与葡萄糖转运蛋白4(GLUT4)的关系。方法:诱导3T3-L1细胞分化,RT-PCR检测GRP120 mRNA表达,油红O染色检测细胞内脂肪;采用siRNA技术下调3T3-L1细胞中GPR120的表达,软脂酸孵育3T3-L1细胞24 h后,用real-time PCR和Western blot方法检测3T3-L1细胞中GLUT4的表达水平的变化。结果:诱导3T3-L1细胞分化过程中GPR120 mRNA表达升高(P<0.05),干扰GPR120表达导致3T3-L1细胞诱导产生的脂滴体积和数量明显减小。另外,干扰GPR120表达导致GLUT4 mRNA和蛋白表达水平下降( P<0.05)。结论:GPR120影响了胰岛素信号通路中GLUT4表达水平,推测其参与了胰岛素抵抗的发生。
目的:研究在3T3-L1細胞中G蛋白偶聯受體120(GPR120)與葡萄糖轉運蛋白4(GLUT4)的關繫。方法:誘導3T3-L1細胞分化,RT-PCR檢測GRP120 mRNA錶達,油紅O染色檢測細胞內脂肪;採用siRNA技術下調3T3-L1細胞中GPR120的錶達,軟脂痠孵育3T3-L1細胞24 h後,用real-time PCR和Western blot方法檢測3T3-L1細胞中GLUT4的錶達水平的變化。結果:誘導3T3-L1細胞分化過程中GPR120 mRNA錶達升高(P<0.05),榦擾GPR120錶達導緻3T3-L1細胞誘導產生的脂滴體積和數量明顯減小。另外,榦擾GPR120錶達導緻GLUT4 mRNA和蛋白錶達水平下降( P<0.05)。結論:GPR120影響瞭胰島素信號通路中GLUT4錶達水平,推測其參與瞭胰島素牴抗的髮生。
목적:연구재3T3-L1세포중G단백우련수체120(GPR120)여포도당전운단백4(GLUT4)적관계。방법:유도3T3-L1세포분화,RT-PCR검측GRP120 mRNA표체,유홍O염색검측세포내지방;채용siRNA기술하조3T3-L1세포중GPR120적표체,연지산부육3T3-L1세포24 h후,용real-time PCR화Western blot방법검측3T3-L1세포중GLUT4적표체수평적변화。결과:유도3T3-L1세포분화과정중GPR120 mRNA표체승고(P<0.05),간우GPR120표체도치3T3-L1세포유도산생적지적체적화수량명현감소。령외,간우GPR120표체도치GLUT4 mRNA화단백표체수평하강( P<0.05)。결론:GPR120영향료이도소신호통로중GLUT4표체수평,추측기삼여료이도소저항적발생。
Objective:To investigate the correlation between G protein-coupled receptor 120 ( GPR120 ) and glucose transporter 4 (GLUT4) in 3T3-L1 cells.Methods:3T3-l1 cells were induced for differentiation,GRP120 mRNA was detected by RT-PCR and Oil red O was used to determine fat expression.GPR120 expression was knocked down by a specific siRNA in 3T3-L1cells.3T3-L1 cell that were tranfected with GPR120 siRNA were incubated with palmitic acid for 24 hours.Then,real-time PCR and Western blot were used to detect the expression of GLUT4 mRNA and protein.Results: Induced differentiation led to GPR120 overexpression in 3T3-L1 cells ( P<0.05 ).GPR120 knockdown resulted in reduction of both lipid volume and number in 3T3-L1 cells.Furthermore,GPR120 knockdown decreased GLUT4 mRNA and protein levels in 3T3-L1 cells (P<0.05,respectively).Conclusion:GPR120 affects the expression level of GLUT4 in insulin signaling pathway,suggesting its involvement in the initiation of insulin resist-ance.