cd154诱导的滑膜液巨噬细胞产生白细胞介素-12的调控。

Arthritis Research Pub Date : 2002-01-01 Epub Date: 2002-07-26 DOI:10.1186/ar589
Milja Möttönen, Pia Isomäki, Reijo Luukkainen, Olli Lassila
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引用次数: 13

摘要

白细胞介素(IL)-12是诱导辅助性T (Th) 1分化和炎症反应的主要细胞因子,被认为是类风湿关节炎(RA)滑膜炎症的重要介质。然而,IL-12在RA中的调控作用尚未阐明。我们的知识主要基于对IL-12p40产生的研究,而不是功能性IL-12p70异源二聚体的研究。我们研究了cd154诱导RA患者滑液(SF)巨噬细胞产生IL-12p40和IL-12p70。CD40结扎可诱导IL-12p40分泌,但不能诱导IL-12p70分泌。观察到IL-10和肿瘤坏死因子(TNF)- α产生的增加表明SF巨噬细胞对CD40连接有反应。p40 mRNA的表达在CD40连接后显著增加并保持上调,而p35转录物的表达仅在短暂且较低水平上增加。我们进一步观察到,从SF巨噬细胞中提取的树突状细胞(DCs)产生IL-12p70。最重要的是,IL-4和IL-13诱导SF巨噬细胞产生IL-12p70,而与正常外周血单核细胞相比,未观察到ifn - γ在这些细胞中激活IL-12p70的产生。这些结果为RA中IL-12p70的产生调控和细胞因子网络的功能提供了新的信息。
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Regulation of CD154-induced interleukin-12 production in synovial fluid macrophages.

Interleukin (IL)-12, being a major cytokine that induces T helper (Th) 1 differentiation and inflammatory response, has been postulated to be an important mediator of synovial inflammation in rheumatoid arthritis (RA). However, the regulation of IL-12 production in RA has not been elucidated. Our knowledge is mainly based on studies of the production of IL-12p40 and not the functional IL-12p70 heterodimer. We have studied the CD154-induced IL-12p40 and IL-12p70 production by synovial fluid (SF) macrophages from patients with RA. CD40 ligation induced the secretion of IL-12p40 but not IL-12p70. The observed increase in IL-10 and tumor necrosis factor (TNF)-alpha production indicated that SF macrophages responded to CD40 ligation. The expression of p40 mRNA was increased significantly and remained upregulated after CD40 ligation, whereas the increase of p35 transcript expression was observed only transiently and at a lower level. We further observed that dendritic cells (DCs) derived in vitro from SF macrophages produced IL-12p70. Most importantly, IL-4 and IL-13 primed SF macrophages to produce IL-12p70, whereas IFN-gamma was not observed to activate IL-12p70 production in these cells, in contrast with normal peripheral blood monocytes. These results provide novel information about the regulation of IL-12p70 production and the function of the cytokine network in RA.

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