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A quantitative bioassay for HIV-1 gene expression based on UV activation: effect of glycyrrhizic acid.

机译:基于紫外线激活的HIV-1基因表达的定量生物测定:甘草酸的作用。

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摘要

Previous reports have shown that HIV-LTRcat constructs stably transfected in HeLa cells are inducible after exposure to UV light. We have optimized this system for studying the effect of drugs on HIV-1 gene expression. The maximum UV response was observed in quiescent stationary cells stimulated with fresh medium for 3h. Glycyrrhizic acid suppressed UV-induced HIV gene expression in a concentration-dependent manner. The inhibitory effect was strongest when GL was added immediately after UV exposure; it was still evident when GL was added at 5 h, it was completely lost at 10 h, after UV exposure. The inhibitory effect was even more pronounced if the cells were pretreated with sub-effective dose (0.0012 mM) of GL prior to UV exposure. The IC50 values with and without pretreatment were 0.04 and 0.38 mM, respectively. Cell proliferation and viability were not affected by GL at doses as high as 2.4 mM. The inhibitory effect of GL on UV-induced CAT activity correlated with the complete inhibition of binding activities of NF-kappaB p65, NF-kappaB p50, c-Fos, and c-Rel. Thus, the UV-based bioassay as proposed here can be exploited for the routine screening of the compounds that interfere with HIV-1 gene expression.
机译:先前的报道表明,在HeLa细胞中稳定转染的HIV-LTRcat构建体在暴露于紫外线后是可诱导的。我们已经优化了该系统,以研究药物对HIV-1基因表达的影响。在用新鲜培养基刺激3h的静态静止细胞中观察到最大的紫外线响应。甘草酸以浓度依赖的方式抑制紫外线诱导的HIV基因表达。紫外线暴露后立即添加GL时,抑制作用最强。仍然很明显,当在GL暴露5小时后加入GL,在暴露于紫外线10个小时后它完全消失了。如果在紫外线照射前用亚有效剂量(0.0012 mM)的GL预处理细胞,则抑制作用会更加明显。有和没有预处理的IC50值分别为0.04和0.38 mM。在高达2.4 mM的剂量下,GL不影响细胞增殖和生存能力。 GL对UV诱导的CAT活性的抑制作用与NF-κBp65,NF-κBp50,c-Fos和c-Rel的结合活性的完全抑制有关。因此,本文提出的基于紫外线的生物测定方法可用于常规筛选干扰HIV-1基因表达的化合物。

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