惠斌, 耿美玉, 李静. 硫酸多糖聚甘古酯抑制HIV-1反式转录调节蛋白诱导的THP-1细胞炎症细胞因子释放及机制探讨J. 药学学报, 2006, 41(4): 338-341.
引用本文: 惠斌, 耿美玉, 李静. 硫酸多糖聚甘古酯抑制HIV-1反式转录调节蛋白诱导的THP-1细胞炎症细胞因子释放及机制探讨J. 药学学报, 2006, 41(4): 338-341.
HUI Bin, GENG Mei-yu, LI Jing. Effect of sulfated polymannuroguluronate on Tat induced proinflammatory cytokines release in THP-1 cells and its mechanism of actionJ. Acta Pharmaceutica Sinica, 2006, 41(4): 338-341.
Citation: HUI Bin, GENG Mei-yu, LI Jing. Effect of sulfated polymannuroguluronate on Tat induced proinflammatory cytokines release in THP-1 cells and its mechanism of actionJ. Acta Pharmaceutica Sinica, 2006, 41(4): 338-341.

硫酸多糖聚甘古酯抑制HIV-1反式转录调节蛋白诱导的THP-1细胞炎症细胞因子释放及机制探讨

Effect of sulfated polymannuroguluronate on Tat induced proinflammatory cytokines release in THP-1 cells and its mechanism of action

  • 摘要: 目的观察硫酸多糖聚甘古酯(SPMG)对HIV-1反式转录调节蛋白(Tat)刺激THP-1细胞释放具有神经毒性的炎症细胞因子如TNFα,IL-1β和IL-6的影响,并探讨其作用机制。方法用ELISA法检测 SPMG 对Tat刺激4 h细胞上清液TNFα、刺激6 h细胞上清液IL-1β和IL-6的影响;用Western blotting技术检测SPMG对PKCζ,PKCθ与PKCδ磷酸化影响。结果SPMG(50~100 μg·mL-1)显著抑制Tat诱导的TNFα,IL-1β与IL-6释放;Tat显著促进PKCζ,PKCθ和PKCδ的磷酸化,SPMG对PKCζ与PKCθ的磷酸化没有影响,但显著抑制PKCδ的磷酸化。结论SPMG可能通过抑制Tat对PKCδ活化,抑制炎症细胞因子TNFα,IL-6与IL-1β释放。

     

    Abstract: AimTo investigate the effects of sulfated polymannuroguluronate (SPMG), a novel candidate anti-AIDS drug in Phase II clinical trial, on Tat-induced release of proinflammatory cytokines (i.e., TNFα, IL-1β and IL-6) and its related mechanism. MethodsThe effects of SPMG on Tat induced TNFα (4 h), IL-1β and IL-6 (6 h) secretion in THP-1 cells were measured by ELISA. Western blotting analysis was used to study the effects of SPMG on Tat induced PKCζ, PKCθ and PKCδ phosphorylation. ResultsSPMG (50 to 100 μg·mL-1) markedly suppressed TNFα IL-1β and IL-6 secretion in Tat activated THP-1 cells. In THP-1 cells the phosphorylation levels of PKCζ, PKCθ and PKCδ significantly increased following Tat stimulation, and only PKCδ phosphorylation levels was inhibited by SPMG (50 to 100 μg·mL-1). ConclusionSPMG suppresses the secretion of proinflammatory cytokines in THP-1 cells may be by inhibiting PKCδ activation.

     

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