形成三螺旋DNA的寡核苷酸抑制内皮细胞组织因子基因的表达
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国家自然科学基金 ( 39970 2 6 9)资助


The Inhibitory Effect of a Triple Helix-Forming Oligonucleotides on the Expression of Tissue Factor Gene in Endothelial Cells
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    摘要:

    为探讨形成三螺旋DNA的寡核苷酸是否对切应力诱导内皮细胞组织因子基因表达有抑制作用,针对内皮细胞组织因子基因启动子内切应力反应元件,设计反向脱氧寡核苷酸序列T21GTa,采用固相亚磷酰胺三酯固相法合成脱氧寡核苷酸。在脱氧寡核苷酸的3’末端进行硫代磷酸酯修饰。应用电泳迁移分析观察寡核苷酸和硫代脱氧寡核苷酸的亲和性。在ECV304内皮细胞株观察γ32P标记硫代磷酸酯三螺旋DNA寡核苷酸的细胞摄取及其对组织因子基因表达的影响。结果发现,硫代磷酸酯寡核苷酸T21GTaps与靶序列能形成三链DNA,其Kd值为3.6×1010molL。在内皮细胞株ECV304细胞,三螺旋DNA寡核苷酸ps(T21GTaps)的细胞吸收率为11.65%,主要分布在核沉淀,约占吸收总量的77.25%,显著降低内皮细胞组织因子基因mRNA表达及组织因子蛋白合成的平均吸光度值,显著降低组织因子的促凝活性。此结果提示,硫代磷酸酯寡核苷酸T21GTaps对内皮细胞组织因子基因表达具有较好的抑制作用

    Abstract:

    Aim The purpose of the present work was to study the inhibitory effect of a triple helix forming oligonucleotides (TFO) on expression of tissue factor (TF) gene in endothelial cells. Methods Antiparallel oligonucleotides T21GTa sequence targeted to shear stress responese element in promoter of TF gene were designed and synthesized by phosphoramidite method and decorated with all PS alinkage. The affinity of TFO and TFO ps were determined by electrophoretic mobility shift assays. Cellular uptake of γ 32 P labelled TFO ps and the effect of TFO ps on expression of TF gene were observed in ECV304 endothelial cell strain. Results TFO ps (T21GTa ps) formed a triplex binding in antiparallel orientation to the puring rich target strand SSRE, with the Kd 3.6×10 10 mol/L. In endothelial cell strand ECV304 the celluar uptake rate of TFO ps (T21GTa ps) is about 11.65%, mainly localized within the nucleus sediment (77.25%),significantly lower the mRNA expression of and the protein synthesis of TF gene, strikingly decreased the coagulation activity of TF. Conclusions TFO ps(T21GTa ps) have significantly inhibited expression of TF gene in endothelial cell.

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李黔宁,应大君,戴光明,郑健,肖道虹,邓志宽,刘勇,刘立杰,周永琴,任萍.形成三螺旋DNA的寡核苷酸抑制内皮细胞组织因子基因的表达[J].中国动脉硬化杂志,2002,10(3):190~194.

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  • 收稿日期:2001-10-08
  • 最后修改日期:2002-03-20
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