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Luteolin inhibits respiratory syncytial virus replication by regulating the MiR-155/SOCS1/STAT1 signaling pathway

机译:叶黄素通过调节MIR-155 / SOCS1 / Stat1信号通路来抑制呼吸道同性恋病毒复制

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摘要

Luteolin inhibits RSV replication in A549 cells and MEFs. a Chemical structure of luteolin. b A549 cells were treated with the indicated concentrations of luteolin for 24, 48, 72, 96 and 120 h. Cell proliferation was measured by CCK-8 assay. c A549 cells were pre-treated with the indicated concentrations of luteolin for 24 h before infected with RSV at MOI = 0.05. After infection for 12, 24, 48, 72 and 96 h, cell culture medium was collected for plaque assay to determine the virus titer. A549 cells, MEFs and HPAEpiC cells were pre-treated with the indicated concentrations of luteolin for 24 h before infected with RSV at MOI = 0.05. At the indicated hours post infection, d virus titer was determined by plaque assay and e RSV-F mRNA expression was determined by RT-qPCR. f A549 cells were pre-treated or treated simultaneously with RSV infection or treated after RSV infection at MOI = 0.05. 48 h post infection, cell culture medium was collected for plaque assay to determine the virus titer. Data shown are means ± SEM. Statistical significance was examined by Students’ t-test. P < 0.05 was considered statistically significant. *P < 0.05, **P < 0.01, ***P < 0.001. RSV respiratory syncytial virus,; CCK-8 Cell Counting Kit-8, MOI multiplicity of infection
机译:叶氏菌素抑制A549细胞和MEF中的RSV复制。叶黄素的化学结构。 B A549细胞用指定的浓度的曲氏菌素治疗24,48,72,96和120h。通过CCK-8测定法测量细胞增殖。在Moi = 0.05的RSV感染之前,用指定的叶英蛋白预处理C a 549细胞预处理。在感染12,24,48,72和96小时后,收集细胞培养基以用于斑块测定以确定病毒滴度。在MOI = 0.05的RSV感染之前,预处理A549细胞,MEF和HPAEPIC细胞预处理24小时的浓度= 0.05。在发布后的时间后,通过斑块测定法测定D病毒滴度,通过RT-QPCR测定E RSV-F mRNA表达。在MOI = 0.05的RSV感染后,预处理或治疗F A549细胞同时处理或治疗。 48小时后感染后,收集细胞培养基用于斑块测定以确定病毒滴度。显示的数据是平均值±SEM。学生的T检验检查了统计学意义。 P <0.05被认为是统计学意义。 * P <0.05,** P <0.01,*** P <0.001。 RSV呼吸道合胞病毒,; CCK-8细胞计数套件-8,MOI多重感染

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