RNA干扰下调小鼠心肌细胞可溶性环氧化物水解酶的表达
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Knockdown of Soluble Epoxide Hydrolase by RNA Interference in Mice Cardiomyocytes
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    目的构建含有可溶性环氧化物水解酶基因特异性的RNA干扰序列pSUPER retro neo质粒载体,选择性下调小鼠心肌细胞可溶性环氧化物水解酶的表达,筛选出抑制效果最明显的表达质粒。方法构建2条靶向可溶性环氧化物水解酶基因的特异性小干扰RNA质粒载体(EH-1和EH-2),以含非特异性小干扰RNA编码序列的质粒载体为阴性对照(pCN组),用FuGENE HD将质粒转染入原代培养的小鼠心肌细胞,并设空白对照组,转染后通过半定量RT-PCR和Western Blotting法,检测可溶性环氧化物水解酶的mRNA和蛋白表达情况。结果与空白对照组、阴性对照组和EH-1组相比,质粒EH-2使心肌细胞可溶性环氧化物水解酶mRNA和蛋白的相对表达量明显下调(分别为0.202±0.017和0.212±0.029,P<0.01)。结论构建了特异性小干扰RNA质粒表达载体,利用RNA干扰技术成功下调了原代培养的心肌细胞中可溶性环氧化物水解酶的表达,为进一步进行心肌细胞的RNA干扰研究奠定了基础。

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    Aim To construct the soluble epoxide hydrolase(sEH) gene-specific recombinant vectors pSUPER retro neo,and selectively knockdown the expression of sEH in mice cardiomyocytes by RNA interference(RNAi),and to select the plasmids having the best silence effect to sEH. Methods Two pairs of siRNA that target at sEH gene were designed,and to construct the siRNA expression vectors specific to sEH gene(EH-1 and EH-2).There were plasmids carrying a nonspecific siRNA coding sequence(pCN) as the negative control group and the blank control group involved.Then the plasmids were transfected into primary cultured mice cardiomyocytes by FuGENE HD.The mRNA and protein expressions of sEH were analyzed by RT-PCR and Western Blotting respectively. Results The expressions of mRNA and protein of sEH in EH-2 group(0.202±0.017 and 0.212±0.029,P<0.01) were significantly decreased compared with that of blank control group,negative control group,and EH-1 group. Conclusion Recombinant expression vectors have been constructed,and RNA interference can selectively knockdown sEH expression in cultured cardiomyocytes.This lays a foundation for further research of RNAi on cardiomyocytes.

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杜广胜,, 文渊, 马业新. RNA干扰下调小鼠心肌细胞可溶性环氧化物水解酶的表达[J].中国动脉硬化杂志,2011,19(3):206~210.

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  • 收稿日期:2011-01-07
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