LRP16蛋白在3T3-L1前脂肪细胞诱导分化中表达量的变化

Expression of LRP16 protein during 3T3-L1 preadipocyte differentiation

  • 摘要: 目的 LRP16蛋白在3T3-L1前脂肪细胞诱导分化过程中表达量的变化及胰岛素对脂肪细胞LRP16蛋白表达的调控。方法 经典脂肪细胞诱导方案诱导前脂肪细胞为成熟脂肪细胞,每天(0-8d)均留取蛋白标本。不同浓度(0、1、10、100nmol/L)胰岛素刺激脂肪细胞24h,分别留取蛋白标本。Western-Blot方法检测样本中LRP16蛋白的表达量。结果 LRP16蛋白在前脂肪细胞无表达或极低表达,从诱导的第3、4天开始表达,迅速升至高峰,此后维持在高表达水平。LRP16蛋白在第6-8天之间表达水平无统计学差异(P>0.05),其余各时段间表达水平均有显著差异(P<0.01)。不同浓度胰岛素刺激脂肪细胞24h,细胞中LRP16蛋白表达量与胰岛素浓度呈负相关(P<0.01)。结论 LRP16蛋白随着前脂肪细胞分化的开启,表达量从无到有逐渐增加至高峰,并一直维持在高表达水平;胰岛素(INS)负调控脂肪细胞LRP16蛋白的表达。

     

    Abstract: Objective To study the expression levels of LRP16 protein in 3T3-L1 preadipocyte differentiation and the effect of insulin on LRP16 protein expression in LRP16 cells.Methods 3T3-L1 preadipocytes were cultured in vitro and differentiated into matured adipocytes,then protein samples were collected everyday(0-8d).Insulin was added into the culture medium of adipocytes for 24h at different concentrations(0,1,10,100nmol/L),and then protein samples were collected.Expression levels of LRP16 protein in 3T3-L1 cells were measured by Western blot.Results LRP16 protein was not expressed or very weakly expressed in preadipocytes.The expression level of LRP16 protein increased rapidly from the day 3 or day 4 and reached its peak on day 7(P<0.01) and then maintained there.No statistical difference was observed in expression of LRP16 protein on days 6-8(P>0.05).The insulin concentration was negatively correlated with the expression level of LRP16 protein in adipocytes after stimulated by insulin for 24h(P<0.01).Conclusion LRP16 protein expression level increases with the differentiation of 3T3-L1 adipocytes,gradually reaches its peak and then maintains there.Insulin down-regulates the expression of LRP16 protein in adipocytes.

     

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