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首页> 外文期刊>Clinical and experimental rheumatology >Increased expression of S100 calcium binding protein A8 in GM-CSF-stimuIated neutrophils leads to the increased expressions of IL-8 and IL-16
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Increased expression of S100 calcium binding protein A8 in GM-CSF-stimuIated neutrophils leads to the increased expressions of IL-8 and IL-16

机译:GM-CSF刺激的中性粒细胞中S100钙结合蛋白A8的表达增加导致IL-8和IL-16的表达增加

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Objectives In our previous proteomic surveillance, we found that at least 11 proteins in neutrophils were increased more than 2.5-fold by the stimulation ofGM-CSF. In this paper, focusing on one of the 11 proteins, S100 calcium binding protein A8 (S100A8), we tried to elucidate the effect ofS100A8 and the cooperative effect ofSWOAS and GM-CSF on production and secretion of cytokines of neutrophils. Methods S100A8 in neutrophil was detected by western blotting, and concentrations ofS100A8 in synovia! fluid (SF) from patients with rheumatoid arthritis (RA) and osteoarthritis (OA) were measured by ELISA. Cytokine levels in the culture medium of neutrophils incubated with and without S100A8 were measured by an antibody array. IL-8 and IL-16 levels in the culture medium of neutrophils stimulated with S100A8, GM-CSF, and the combination ofS100A8 and GM-CSF were measured by ELISA. The mRNA levels of IL-8 and IL-16 in the stimulated neutrophils were analysed by real-time PCR. Results The western blotting analysis confirmed that S100A8 is up-regulated in neutrophil by the stimulation of GM-CSF. Furthermore, the ELISA analysis confirmed that S100A8 was significantly elevated in SF of patients with RA compared to SF of patients with OA. S100A8 induced mRNA expression and secretion of IL-8 and IL-16. S100A8 further enhanced production of IL-8 by GM-CSF but not that of IL-16. Conclusions These data suggest that S100A8 may be involved in the exacerbation ofRA, and that S100A8 may be a therapeutic target of RA.
机译:目的在我们以前的蛋白质组学监测中,我们发现通过刺激GM-CSF,嗜中性粒细胞中至少有11种蛋白质增加了2.5倍以上。在本文中,我们着眼于11种蛋白中的一种,即S100钙结合蛋白A8(S1​​00A8),试图阐明S100A8的作用以及SWOAS和GM-CSF对中性粒细胞的细胞因子产生和分泌的协同作用。方法采用蛋白印迹法检测中性粒细胞中的S100A8,并测定滑膜中S100A8的浓度。用ELISA法测量类风湿关节炎(RA)和骨关节炎(OA)患者的体液(SF)。通过抗体阵列测量在有和没有S100A8的情况下培养的嗜中性白细胞的培养基中的细胞因子水平。通过ELISA测量了用S100A8,GM-CSF刺激的中性粒细胞培养基中的IL-8和IL-16水平,以及S100A8和GM-CSF的组合。通过实时PCR分析刺激的中性粒细胞中IL-8和IL-16的mRNA水平。结果蛋白质印迹分析证实,通过刺激GM-CSF,嗜中性粒细胞中S100A8被上调。此外,ELISA分析证实与OA患者的SF相比,RA患者的SF中S100A8显着升高。 S100A8诱导IL-8和IL-16的mRNA表达和分泌。 S100A8进一步增强了GM-CSF产生IL-8的能力,但没有增强IL-16的产生。结论这些数据表明S100A8可能参与RA的恶化,并且S100A8可能是RA的治疗靶标。

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