首页> 外文期刊>Thrombosis Research: An International Journal on Vascular Obstruction, Hemorrhage and Hemostasis >The effect of number of days in culture and plasminogen activator inhibitor-1 (PAI-1) 4G/5G genotype on PAI-1 antigen release by cultured human umbilical vein endothelial cells.
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The effect of number of days in culture and plasminogen activator inhibitor-1 (PAI-1) 4G/5G genotype on PAI-1 antigen release by cultured human umbilical vein endothelial cells.

机译:培养天数和纤溶酶原激活物抑制剂1(PAI-1)4G / 5G基因型对培养的人脐静脉内皮细胞释放PAI-1抗原的影响。

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摘要

An insertion/deletion (4G/5G) polymorphism in what has been shown to be an enhancer/repressor binding site in the promoter region of the PAI-1 gene has been related to plasma PAI-1 activity. Transfection studies demonstrated increased interleukin-1 stimulated PAI-1 synthesis in cells containing the 4G sequence. To study this response in endothelial cells, first passage HUVEC from 26 umbilical cords were stimulated with interleukin-1 and tumor necrosis factor-alpha. PAI-1 antigen was measured in 24-hour conditioned medium and allele-specific PCR utilized to determine genotype at the 4G/5G locus. Analysis of covariance was used to determine whether the effect of a variable time in culture was masking a difference between genotypes. A trend towards higher PAI-1 levels with increasing time in culture was observed. The geometric mean (95% confidence interval) of the basal rate of PAI-1 release was, 4G/4G 9.7 (7.0, 13.5) ng/24 hours (n=11), 4G/5G 9.5 (6.5, 13.9) ng/24 hours (n=9), and 5G/5G 10.9 (7.8, 15.1) ng/24 hours (n=6). In cells of the same cultures, the interleukin-1 stimulated levels were 25.9 (23.1, 29.1), 27.2 (23.6, 31.3), and 23.1 (19.5, 27.3) ng/24 hours, respectively, corresponding to ratios of stimulated to basal levels of 2.68, 2.87, and 2.12. After adjustment for time in culture the basal PAI-1 release was 4G/4G 10.7, 4G/5G 9.1, and 5G/5G 9.7 ng/24 hours. For interleukin-1 stimulated release the adjusted levels were 26.3, 27.0, and 22.7 ng/24 hours, respectively. Adjusted levels in 4G/4G genotype cells were non-significantly greater than those in cells of 5G/5G genotype by a factor of 1.16 (0.95, 4.08). This study did not demonstrate a significant difference in basal or cytokine stimulated PAI-1 release from cells of different PAI-1 promoter (4G/5G) genotypes but does not exclude increased interleukin-1 stimulated PAI-1 release in the 4G/4G compared with the 5G/5G genotype.
机译:已经显示出在PAI-1基因的启动子区域中的增强子/阻遏物结合位点的插入/缺失(4G / 5G)多态性与血浆PAI-1活性有关。转染研究表明,在含有4G序列的细胞中,白介素1刺激的PAI-1合成增加。为了研究内皮细胞中的这种反应,用白介素-1和肿瘤坏死因子-α刺激了26条脐带的第一代HUVEC。在24小时条件培养基中测量PAI-1抗原,并利用等位基因特异性PCR来确定4G / 5G位点的基因型。使用协方差分析来确定文化中可变时间的影响是否掩盖了基因型之间的差异。观察到随着培养时间的增加PAI-1水平升高的趋势。 PAI-1释放基础速率的几何平均值(95%置信区间)为4G / 4G 9.7(7.0,13.5)ng / 24小时(n = 11),4G / 5G 9.5(6.5,13.9)ng / 24小时(n = 9)和5G / 5G 10.9(7.8,15.1)ng / 24小时(n = 6)。在相同培养物中的细胞中,白介素1刺激水平分别为25.9(23.1,29.1),27.2(23.6,31.3)和23.1(19.5,27.3)ng / 24小时,分别对应于刺激水平与基础水平的比率分别为2.68、2.87和2.12。调整培养时间后,基础PAI-1释放时间为4G / 4G 10.7、4G / 5G 9.1和5G / 5G 9.7 ng / 24小时。对于白介素1刺激的释放,调整后的水平分别为26.3、27.0和22.7 ng / 24小时。 4G / 4G基因型细胞中的调整水平比5G / 5G基因型细胞中的调整水平显着增加1.16(0.95,4.08)。这项研究没有证明基础或细胞因子刺激的PAI-1从不同PAI-1启动子(4G / 5G)基因型细胞释放的显着差异,但不排除与4G / 4G相比,白介素1刺激的PAI-1释放增加5G / 5G基因型。

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