敲低低密度脂蛋白受体相关蛋白1抑制C3H10T1/2多潜能干细胞定向成脂
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国家重点基础研究发展计划(973)资助项目(2006CB943704, 2009CB825604)


Knock Down of Low Density Lipoprotein Receptor-related Protein 1(Lrp1) by RNAi Inhibits The Commitment of C3H10T1/2 Pluripotent Stem Cells to Preadipocyte
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This work was supported by grants from National Basic Research Program of China (2006CB943704, 2009CB825604)

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    摘要:

    C3H10T1/2多潜能干细胞成脂过程分为定向和分化两个阶段,骨形成蛋白4(BMP4)可以诱导其定向成前脂肪细胞.已有的研究表明,脂肪组织特异性敲除低密度脂蛋白受体相关蛋白1(Lrp1)的小鼠体重减轻,脂肪组织含量减少,揭示此基因对成脂具有重要作用.然而,目前尚不清楚Lrp1是否在成脂定向过程中发挥作用.采用小干扰RNA技术(RNAi),在体外水平研究低密度脂蛋白Lrp1对C3H10T1/2多潜能干细胞成脂定向的作用.分别在C3H10T1/2成脂的定向期和脂滴成熟期敲低Lrp1,通过显微镜下观察、油红O染色、Western blotting等实验证实,定向期而非脂滴成熟期敲低Lrp1显著抑制C3H10T1/2多潜能干细胞成脂.BMP4通过激活下游Smad1/5/8信号通路发挥作用,而敲低Lrp1显著抑制BMP4诱导的Smad1/5/8磷酸化.这些结果说明:敲低Lrp1通过下调Smad信号通路,抑制BMP4诱导的C3H10T1/2多潜能干细胞成脂定向.

    Abstract:

    The adipocyte development process of C3H10T1/2 pluripotent stem cells includes two stages: the commitment stage and the differentiation stage.There are evidences that BMP4 commits C3H10T1/2 cells into preadipocytes.Previous studies have shown that mice lacking adipocyte Lrp1(adLrp1-/-) displays reduced body weight and smaller fat stores which highlights the important role of Lrp1 in adipogenesis.However, little is known about the role of Lrp1 in preadipocyte commitment.RNAi was used to study the effect of low density lipoprotein receptor-related protein 1(Lrp1) on commitment of C3H10T1/2 to preadipocyte.Through microscopic examination, Oil red O staining, Western blotting, it is demonstrated that Lrp1 RNAi inhibits C3H10T1/2 adipogenesis in commitment stage, rather than in lipid maturation period.BMP4 signals through Smad1/5/8 and Lrp1 RNAi significantly suppresses the BMP4-triggered phosphorylation of Smad1/5/8.These data suggest that Lrp1 RNAi has inhibitory effects on the BMP4-induced of C3H10T1/2 preadipocyte commitment via down-regulating Smad signaling.

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陈婧文,郭亮.敲低低密度脂蛋白受体相关蛋白1抑制C3H10T1/2多潜能干细胞定向成脂[J].生物化学与生物物理进展,2012,39(10):987-994

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  • 收稿日期:2011-12-12
  • 最后修改日期:2012-02-23
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  • 在线发布日期: 2012-03-01
  • 出版日期: 2012-10-20