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作 者:郭俊[1] 刘宇[1] 王忠凯[1] 李国然[1] 沈下贤[1] 赵仙先[1]
机构地区:[1]第二军医大学附属长海医院心内科,上海200433
出 处:《现代生物医学进展》2016年第10期1821-1824,共4页Progress in Modern Biomedicine
基 金:国家自然科学基金面上项目(81370266)
摘 要:目的:研究氧化应激诱导的内皮细胞micro RNA的表达变化。方法:ECM(Endothelial Cell Medium)培养人脐静脉内皮细胞,利用不同浓度双氧水(0μmol/L,200μmol/L,500μmol/L,800μmol/L)刺激24小时后应用流式细胞术检测其凋亡水平。提取细胞总RNA,利用实时定量PCR(Quantitive real-time PCR;q RT-PCR)检测micro RNA表达量变化,并利用生物信息学软件预测可能的靶基因。结果:加入不同浓度双氧水处理24 h后的内皮细胞总凋亡率均显著高于对照组,200μmol/L、500μmol/L和800μmol/L组的凋亡率分别为(13.31%vs 4.75%,35.9%vs 4.75%,89.75%vs 4.75%,P<0.01)。200μmol/L的双氧水处理内皮细胞后,micro RNA的表达出现了明显的改变。其中mi R-92a、mi R-126的表达明显下调(P<0.05),mi R-181a、mi R-217、mi R-34a和mi R-320的表达明显上调(P<0.05)。靶基因预测显示mi R-320、mi R-92a可能调控多个和内皮细胞凋亡相关的基因表达。结论:在氧化应激诱导的内皮细胞凋亡中,mi RNA表达发生改变并可能参与调控内皮细胞功能。Objective: To determine the expression change of micro RNA in endothelial cells under oxidative stress. Methods:Human Umbilical Vein Endothelial Cells cultured by ECM, were stimulated by different concentrations of hydrogen peroxide(0 umol/L,200 μmol/L, 500 μmol/L, 800 μmol/L) for 24 hours. Cells apoptosis assessed by Annexin V/PI staining and flow cytometry. Total RNA was isolated from cells, and micro RNA expression levels were detected by using quantitive real-time PCR. Bioinformatics prediction software were applied to predict potential target genes of these mi RNAs. Results: The apoptosis rate of endothelial cells increased significantly after hydrogen peroxide stimulation. Compared with control cells, the apoptosis rate of 200 μmol/L, 500 μmol/L and 800μmol/L hydrogen peroxide treatment group were significantly increased(13.31 % vs 4.75 %, 35.9 % vs 4.75 %, 89.75 % vs 4.75 %,respectively, P〈0.01). Quantitive real-time PCR results showed that the expression of mi RNA appeared obviously disorder, of which mi R-92 a, mi R-126 were decreased, while mi R-181 a, mi R-217, mi R-34 a and mi R-320 were increased notably(P〈0.05). Mi R-92 a and mi R-320 might regulate the expression of multiple genes related to the apoptosis of endothelial cells. Conclusion: The abnormal expression mi RNAs in HUVECs after oxidative stress induced apoptosis suggested that these mi RNAs maybe involved in regulation of endothelial cells function.
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