侯琦, 程桂芳, 张成义, 李良成. 4种刺激剂及抗炎药对HL-60细胞生成IL-8的影响J. 药学学报, 2000, 35(3): 173-176.
引用本文: 侯琦, 程桂芳, 张成义, 李良成. 4种刺激剂及抗炎药对HL-60细胞生成IL-8的影响J. 药学学报, 2000, 35(3): 173-176.
Hou Qi Cheng Guifang Zhang Chengyi Li Liangcheng, . EFFECTS OF FOUR STIMULANTS AND ANTI-INFLAMMATORY DRUGS ON PRODUCTION OF INTERLEUKIN-8 IN HL-60 CELLSJ. Acta Pharmaceutica Sinica, 2000, 35(3): 173-176.
Citation: Hou Qi Cheng Guifang Zhang Chengyi Li Liangcheng, . EFFECTS OF FOUR STIMULANTS AND ANTI-INFLAMMATORY DRUGS ON PRODUCTION OF INTERLEUKIN-8 IN HL-60 CELLSJ. Acta Pharmaceutica Sinica, 2000, 35(3): 173-176.

4种刺激剂及抗炎药对HL-60细胞生成IL-8的影响

EFFECTS OF FOUR STIMULANTS AND ANTI-INFLAMMATORY DRUGS ON PRODUCTION OF INTERLEUKIN-8 IN HL-60 CELLS

  • 摘要: 目的:探讨4种刺激剂脂多糖(LPS)、佛波脂(PMA)、甲酰三肽(fMLP)和钙离子载体A23187及抗炎药物对HL-60细胞生成白细胞介素8(IL-8)的作用。方法:用ELISA方法测定IL-8的含量。结果:LPS对3种浓度HL-60细胞IL-8生成均有刺激作用,PMA,fMLP 0.01,0.1,1,10 nmol.L-1和A23187  0.01,0.1 nmol.L-1亦有明显促进作用。Asp,Sali,Hcort在1×10-5 mol.L-1和Iso 1×10-6~1×10-4 mol.L-1可明显抑制IL-8生成。结论:本研究建立了可靠的筛选IL-8生成抑制剂的模型,表明异丹叶大黄素具有明显的IL-8生成抑制作用。

     

    Abstract: AIM: To study the dose-effects relationship of lipopolysacchride (LPS), phorbol 12-myristate, 13-acetate(PMA), N-formyl-Met-Leu-Phe (fMLP)and calcium ionophore A23187 (A23187) on the production of intrerleukin-8 (IL-8) in cultured HL-60 cells and effects of different densities of HL-60 cells on the production of IL-8 induced by LPS. To observe the effects of several anti-inflammatory drugs, such as aspirin (Asp), indomethacin (Indo), salisylic acid (Sali), meloxicam (Melo) and hydrocortisone (Hcort) on the production of IL-8 induced by LPS in HL-60 cells. METHODS: The HL-60 cells were adjusted to appropriate densities and added to tissue culture plates, then stimulants or vehicle or drugs were added. The plates were incubated at 37℃, 5% CO2 for 24 h, then the supernatants were collected. The concentration of IL-8 in supernatants were measured by ELISA method with the limit of detection at 1.56 pg.mL-1. RESULTS: All of the four stimulants—LPS, fMLP, PMA and A23187 were shown to enhance the secretion of IL-8 in cultured HL-60 cells. Asp, Sali and Hcort at the concentration of 1×10-5 mol.L-1 significantly inhibited IL-8 secretion stimulated by LPS 5 μg.mL-1 for 24 h in HL-60 cells with the inhibition ratio of 86.2, 82.77 and 136.3%, respectively. It was also inhibited by isorhapotigenin at the concentrations from 1×10-6 to 1×10-4 mol.L-1, with IC50 2.23×10-8 mol.L-1. CONCLUSION: An easy and trustworthy method of assay for the production of IL-8 in HL-60 cells was established, which can be used as a model of selecting inhibitors of IL-8 production.

     

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