薛妮娜, 季鸣, 张明祎, 刘羿晨, 陈晓光. IL-17信号通路抑制剂细胞筛选模型的优化及应用J. 药学学报, 2019,54(10): 1858-1862. doi: 10.16438/j.0513-4870.2019-0703
引用本文: 薛妮娜, 季鸣, 张明祎, 刘羿晨, 陈晓光. IL-17信号通路抑制剂细胞筛选模型的优化及应用J. 药学学报, 2019,54(10): 1858-1862. doi: 10.16438/j.0513-4870.2019-0703
XUE Ni-na, JI Ming, ZHANG Ming-yi, LIU Yi-chen, CHEN Xiao-guang. The optimization and application of cell-based screening model for IL-17-mediated signaling pathwayJ. Acta Pharmaceutica Sinica, 2019,54(10): 1858-1862. doi: 10.16438/j.0513-4870.2019-0703
Citation: XUE Ni-na, JI Ming, ZHANG Ming-yi, LIU Yi-chen, CHEN Xiao-guang. The optimization and application of cell-based screening model for IL-17-mediated signaling pathwayJ. Acta Pharmaceutica Sinica, 2019,54(10): 1858-1862. doi: 10.16438/j.0513-4870.2019-0703

IL-17信号通路抑制剂细胞筛选模型的优化及应用

The optimization and application of cell-based screening model for IL-17-mediated signaling pathway

  • 摘要: 本研究摸索及验证HEK-Blue-IL-17细胞模型的筛选条件,并应用该模型筛选抑制IL-17信号通路的化合物。按5×104个/孔的密度,将HEK-Blue-IL-17细胞接种在96孔培养板中,分别加入不同浓度的IL-17A或IL-17F和待筛选化合物培养16 h,移取培养上清与QUANTI-Blue反应1或3 h,在λ655 nm处检测吸光度值。通过碱性磷酸酶(secreted alkaline phosphatase,SEAP)的生成量来反映该细胞模型中IL-17信号通路的活化状态。实验显示:IL-17A和IL-17F均可显著性地激活HEK-Blue IL-17细胞。IL-17A和IL-17F分别在10和100 ng·mL-1剂量下可产生较高的响应值。SEAP与QUANTI-Blue反应1 h基本可达到终点反应。牛蒡子苷元(arctigenin)和表没食子儿茶素没食子酸酯(epigallocatechin gallate,EGCG)对IL-17A和IL-17F刺激的信号通路具有一定的抑制活性。本实验建立并优化了HEK-Blue IL-17细胞模型,可用于IL-17信号通路抑制剂的筛选。

     

    Abstract: We explore and verify the optimized condition for HEK-Blue IL-17 screening model, and screen the compounds that inhibits IL-17-medited signaling pathway. HEK-Blue IL-17 cells (5×104 cells per well) were seeded into the 96 plates followed by different concentrations of IL-17A or IL-17F alone, or in combination with tested compounds for 16 h. Then, the supernatant medium was incubated with QUANTI-Blue for 1 or 3 h to detect the OD value at λ655 nm. The secreted alkaline phosphatase (SEAP) production was an index of IL-17-mediated signaling activation in HEK-Blue IL-17 cells. We found that both IL-17A and IL-17F can significantly activate the IL-17 signaling pathway in HEK-Blue IL-17 cells. The available dosage of IL-17A and IL-17F were 10 and 100 ng·mL-1, respectively. The reaction time of SEAP and QUANTI-Blue was 1 h. In this model, arctigenin and epigallocatechin gallate (EGCG) could inhibit the IL-17A and IL-17F-mediated signaling pathway. This established and optimized screening model of HEK-Blue IL-17 cells was suitable for screening inhibitors of IL-17-mediated signaling pathway.

     

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