任德成, 杜冠华, 张均田. 细胞间粘附分子-1抑制剂的高通量筛选J. 药学学报, 2003, 38(6): 405-408.
引用本文: 任德成, 杜冠华, 张均田. 细胞间粘附分子-1抑制剂的高通量筛选J. 药学学报, 2003, 38(6): 405-408.
REN De-cheng, DU Guan-hua, ZHANG Jun-tian. High throughput screening for intercellular adhesion molecule-1 inhibitorJ. Acta Pharmaceutica Sinica, 2003, 38(6): 405-408.
Citation: REN De-cheng, DU Guan-hua, ZHANG Jun-tian. High throughput screening for intercellular adhesion molecule-1 inhibitorJ. Acta Pharmaceutica Sinica, 2003, 38(6): 405-408.

细胞间粘附分子-1抑制剂的高通量筛选

High throughput screening for intercellular adhesion molecule-1 inhibitor

  • 摘要: 目的建立细胞间粘附分子-1(ICAM-1)抑制剂的高通量筛选方法。方法用脂多糖(LPS)激活原代培养的人脐带内皮细胞,用酶联免疫法(ELISA)测定内皮细胞激活后粘附分子ICAM-1的表达。用MTT法检测所筛化合物的毒性作用。结果LPS时间和剂量依赖性地激活内皮细胞表达ICAM-1, 以质量浓度为1 mg·L-1和刺激时间为24 h为佳。在对2 000个化合物的初筛中,发现30个化合物可抑制ICAM-1的表达,入围率为1.5%,其中24个化合物有细胞毒作用。结论ELISA方法成本低、重复性好,效率高,适合ICAM-1抑制剂的高通量筛选。

     

    Abstract: AimTo develop a high throughput screening assay to identify inhibitors of intercellular adhesion molecule-1 (ICAM-1) expression in human umbilical vein endothelial cells (HUVEC). Methods ICAM-1 expression in lipopolysaccharide-stimulated endothelial cells was measured by ELISA. The cytotoxicity of the compounds was measured by MTT. ResultsLipopolysaccharide (LPS) increased ICAM-1 expression in HUVEC in a concentration- and time-dependent manner. Two thousand compounds were screened and the hit rate was 1.5%. Among these 30 compounds, 24 were cytotoxic.ConclusionThe ELISA method was inexpensive, reproducible and suitable for high throughput primary cell assay. This assay was feasible to identify inhibitors of ICAM-1 and simultaneously discriminate the activity from the cytotoxic effects.

     

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