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作 者:刘佳[1] 秦留安[1] 席少枝[1] 刘军[1] 王绪云[1] 李晓琪[1] 杨洁[1] 尹彤[1]
出 处:《中华老年多器官疾病杂志》2017年第3期208-211,共4页Chinese Journal of Multiple Organ Diseases in the Elderly
基 金:北京市自然科学基金面上项目(7152129);解放军总医院临床扶持基金(2012FC-TSYS-3043)~~
摘 要:目的探索维生素K代谢相关基因CYP4F2对维生素K依赖性凝血因子活化(凝血因子FⅨ为例)的影响。方法构建同时含有CYP4F2-cDNA片段与FⅨ-cDNA片段的pIRES质粒,通过酶切验证。使用Lipofectamine 2000转染试剂,将构建成功的pIRES-FⅨ-CYP4F2质粒以及pIRES-FⅨ质粒、pIRES空白对照质粒瞬时转染LO2细胞。在不同质粒转染的细胞中,通过Western blotting验证CYP4F2和FⅨ蛋白的表达,应用FⅨa Assay检测试剂盒检测FⅨa活性。结果经酶切证实,pIRES-FⅨ-CYP4F2质粒构建成功。Western blotting证实,pIRES-FⅨ及pIRES-FⅨ-CYP4F2质粒成功转染LO2细胞。FⅨa Assay检测发现,在过表达FⅨ的LO2细胞培养上清和细胞裂解液中,FⅨa活性较对照组显著升高;当同时过表达CYP4F2和FⅨ后,LO2细胞培养上清和细胞裂解液中的FⅨa活性较单独过表达FⅨ组明显降低。结论维生素K代谢相关基因CYP4F2的过表达对维生素K依赖性FⅨ的活化具有抑制作用。Objective To determine the effect of vitamin K metabolize associated gene CYP4F2 on the activation of vitamin K dependent coagulation factor Ⅸ(FⅨ).Methods The pIRES plasmid containing CYP4F2-cDNA fragment and FⅨ-cDNA fragment was constructed, and enzyme digestion was used to verify the products .The plasmids pIRES-FⅨ-CYP4F2, pIRES-FⅨ and pIRES (control plasmid) were transfected into LO2 cells respectively with Lipofectamine 2000 transfection reagent.Western blotting was used to detect the expression of CYP 4F2 and FⅨ.The activity of FⅨa was detected by FⅨa activity assay kit .Results The results of enzyme digestion indicated that the pIRES-FⅨ-CYP4F2 plasmid was successfully constructed .The plasmids pIRES-FⅨ and pIRES-FⅨ-CYP4F2 were successfully transfected into LO2 cells.FⅨa activity was significantly higher in the supernatants and cell lysates from the FⅨ-overexpressed LO2 cells than the control cells , but the activity was significantly reduced in the LO 2 cells with the over-expression of FⅨand CYP4F2 than the cells with the over-expression of FⅨ.Conclusion The over-expression of CYP4F2 exerts inhibitory effect on the activation of vitamin K dependent FⅨ.
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