胰岛素受体底物1基因沉默对3T3-L1细胞CCAAT增强子结合蛋白α、过氧化物酶体增殖物激活受体γ表达的影响  被引量:3

Effect of Insulin Receptor Substrate 1 Gene Silence on Expression of CCAAT Enhancer Binding Protein α and Peroxisome Proliferator-Activated Receptor γ in 3T3-L1 Preadipocyte Cell

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作  者:郑锐丹[1] 廖丽红[1] 王成斌[1] 高金枝[1] 应艳琴[1] 宁琴[1] 罗小平[1] 

机构地区:[1]华中科技大学同济医学院附属同济医院儿科,武汉430030

出  处:《实用儿科临床杂志》2012年第7期482-485,共4页Journal of Applied Clinical Pediatrics

基  金:国家自然科学基金(30672262)

摘  要:目的研究胰岛素受体底物1(IRS-1)沉默对3T3-L1前脂肪细胞分化关键分子CCAAT增强子结合蛋白α(C/EBPα)、过氧化物酶体增殖物激活受体γ(PPARγ)mRNA及蛋白表达的影响,并观察IRS-1沉默后前脂肪细胞分化为成熟脂肪细胞能力的改变,探讨胰岛素受体底物(IRSs)是否作为C/EBPα、PPARγ的上游调节信号在前脂肪细胞分化中起到重要的调节作用。方法合成4条IRS-1 shRNA,Western blotting筛选出沉默效率最高的1条。3T3-L1前脂肪细胞分为IRS-1沉默组和对照组。IRS-1沉默组细胞用沉默效率最高的IRS-1 shRNA质粒转染3T3-L1前脂肪细胞,沉默细胞中的IRS-1分子;对照组采用无意义IRS-1 shRNA质粒转染3T3-L1前脂肪细胞。转染24 h后诱导其分化成熟,分化72 h后检测促进前脂肪细胞分化的关键分子C/EBPα、PPARγ的表达。继续诱导分化至第7天,油红O染色观察IRS-1沉默后前脂肪细胞分化为成熟脂肪细胞的比例,检测其分化能力的改变。结果与对照组相比,IRS-1沉默组在诱导分化72 h后,Real-time PCR结果显示3T3-L1前脂肪细胞中C/EBPαmRNA、PPARγmRNA表达明显下降(Pa<0.05),Western blotting结果显示C/EBPα、PPARγ蛋白水平也同样显著下降(Pa<0.05);细胞继续分化至第7天,油红O染色显示,IRS-1沉默组前脂肪细胞分化成熟的比例与对照组比较显著降低。结论胰岛素可能通过IRS-1刺激C/EBPα、PPARγ的表达促进前脂肪组织的分化。Objective To examine the influence of insulin receptor substrate 1 ( IRS - 1 ) gene silence on the mRNA and protein expres- sion of CCAAT enhancer binding protein α (C/EBPα ) and peroxisome proliferator - activated receptor γ(PPARγ) in 333 - L1 preadipocyte cell, to observe the changes of its differentiation ability into mature cell when IRS - 1 gene was silenced, and explore whether IRS - 1 was a key upstream regulatory molecule of C/EBPα and PPARγ in preadipocyte cell differentiation. Methods Four recombination plasmids of IRS - 1 shRNA were constructed and the most effective one was selected by Western blotting. The cells infected with the most effective IRS - 1 shRNA plasmid were grouped as IRS - 1 silence group and cells incubated with non - sense IRS - 1 shRNA as control group. The cells were induced into mature cell after 24 hours' incubation with transfection. The expression levels of mRNA and protein of C/EBPα and PPARγ/were tested by Western blotting and real -time PCR, and the differentiation level was examined by red oil, respectively, at 72 h and 7 d after the differentiation. Results Compared with the control group, both mRNA and protein expression of C/EBPα and PPARα in IRS - 1 silence group had significant decrease at 72 h after the ceils differentiation (Pa 〈 0.05 ), and the ratio of mature cells which was tested by red oil reduced obviously in IRS - 1 silence group at 7 d after the differentiation. Conclusion Insulin can stimulate the expression of C/EBPα and PPARγ/by IRS - 1 in order to promote preadipocyte cells differentiation.

关 键 词:胰岛素受体底物1 RNA干扰 CCAAT增强子结合蛋白α 过氧化物酶体增殖物激活受体Γ 3T3-L1前脂肪细胞 

分 类 号:R363[医药卫生—病理学]

 

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