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首页> 外文期刊>Clinical and Experimental Immunology: An Official Journal of the British Society for Immunology >A form of circulating interleukin-6 receptor component soluble gp130 as a potential interleukin-6 inhibitor in inflammatory bowel disease.
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A form of circulating interleukin-6 receptor component soluble gp130 as a potential interleukin-6 inhibitor in inflammatory bowel disease.

机译:一种循环白细胞介素-6受体组分可溶性GP130的形式作为炎性肠病患者的潜在白细胞介素-6抑制剂。

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The presence and the role of soluble gp130, the soluble form of a component of the interleukin (IL)-6 receptor complex, were investigated in inflammatory bowel disease. The serum concentrations of soluble gp130 were increased in ulcerative colitis (active disease, median, 93.5 ng/ml; interquartile range, 26-125 ng/ml; inactive disease, 81 ng/ml, 24.8-137.3 ng/ml) and to a lesser extent in Crohn's disease (active disease, 66 ng/ml, 44.4-87.6 ng/ml; inactive disease, 63 ng/ml, 43.5-82.5 ng/ml) compared to normal controls (43 ng/ml, 27-59 ng/ml). Paired analysis of serum samples showed a decrease of IL-6 and soluble IL-6 receptor concentrations in both diseases and an increase of soluble gp130 concentrations, especially in ulcerative colitis, just after the resolution of disease exacerbation. Size fractionation of the serum revealed that a part of the IL-6 co-eluted with soluble gp130 and soluble IL-6 receptor. The IL-6-induced proliferation of murine B9 hybridoma was enhanced by recombinant soluble IL-6 receptor, whereas the proliferation was inhibited by recombinant soluble gp130. These results indicate that soluble gp130 may function as a natural inhibitor of the IL-6 actions in inflammatory bowel disease.
机译:可溶性GP130的存在和作用,在炎性肠病中研究了白细胞介素(IL)-6受体复合物复合物的可溶性形式的组分。可溶性GP130的血清浓度在溃疡性结肠炎(活性疾病,中值,93.5ng / ml;四分位数范围,26-125ng / ml;非活性疾病,81ng / ml,24.8-137.3ng / ml)和a克罗恩病的程度较小(活性疾病,66ng / ml,44.4-87.6ng / ml;与正常对照相比,63ng / ml,43.5-82.5ng / ml)(43ng / ml,27-59 ng / ml)。血清样品的成对分析显示IL-6和可溶性IL-6受体浓度在疾病和可溶性GP130浓度的增加,特别是在溃疡性转化后的溃疡性结肠炎。血清的大小分馏显示,IL-6的一部分用可溶性GP130和可溶性IL-6受体共洗。通过重组可溶性IL-6受体增强了IL-6诱导的鼠B9杂交瘤的增殖,而通过重组可溶性GP130抑制增殖。这些结果表明,可溶性GP130可以用作炎性肠病中IL-6作用的天然抑制剂。

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