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白细胞介素-4与粒细胞-巨噬细胞集落刺激因子或白细胞介素-3协同作用对人单核细胞诱导CD23表达的影响:干扰素-α和干扰素-γ的调节作用

Synergistic effects of IL-4 and either GM-CSF or IL-3 on the induction of CD23 expression by human monocytes: regulatory effects of IFN-alpha and IFN-gamma.

作者信息

Alderson M R, Armitage R J, Tough T W, Ziegler S F

机构信息

Department of Cellular Immunology, Immunex Research and Development Corporation, Seattle, WA 98101.

出版信息

Cytokine. 1994 Jul;6(4):407-13. doi: 10.1016/1043-4666(94)90065-5.

DOI:10.1016/1043-4666(94)90065-5
PMID:7948749
Abstract

CD23 expression by B cells and monocytes can be regulated by cytokines including IL-4, IFN-gamma and IFN-alpha. We recently reported that GM-CSF and IL-3 are also capable of regulating CD23 expression, with GM-CSF enhancing CD23 expression by monocytes and IL-3 enhancing CD23 expression by both monocytes and B cells. In this study, we have assessed the effect of combinations of cytokines on monocyte CD23 expression. IL-4 acted in a synergistic manner with either GM-CSF or IL-3 to induce monocyte CD23 expression. Interestingly, culture of monocytes with GM-CSF, IL-3 or IL-4 resulted in two subpopulations of cells, one negative or dull for surface CD23 and the other expressing relatively high levels of CD23. In contrast, culturing monocytes in the combination of IL-4 with either GM-CSF or IL-3 resulted in a single population of cells expressing very high levels of CD23. The synergy between IL-4 and either GM-CSF or IL-3 was also reflected at the level of release of soluble CD23 and CD23 mRNA expression and was seen at both sub-optimal and optimal cytokine concentrations. GM-CSF, IL-3 and IL-4 all enhanced monocyte expression of class II MHC, though no additive or synergistic effects were seen with cytokine combinations. IFN-gamma failed to induce monocyte CD23 expression when acting alone, though it enhanced both surface and soluble CD23 when acting in the presence of GM-CSF, IL-3 or IL-4. In contrast, IFN-alpha was a potent inhibitor of monocyte CD23 expression induced by these three cytokines.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

B细胞和单核细胞的CD23表达可受包括白细胞介素-4(IL-4)、γ干扰素(IFN-γ)和α干扰素(IFN-α)在内的细胞因子调控。我们最近报道,粒细胞-巨噬细胞集落刺激因子(GM-CSF)和白细胞介素-3(IL-3)也能够调控CD23表达,GM-CSF可增强单核细胞的CD23表达,IL-3则可增强单核细胞和B细胞的CD23表达。在本研究中,我们评估了细胞因子组合对单核细胞CD23表达的影响。IL-4与GM-CSF或IL-3协同作用诱导单核细胞CD23表达。有趣的是,用GM-CSF、IL-3或IL-4培养单核细胞会产生两个细胞亚群,一个表面CD23呈阴性或弱阳性,另一个表达相对高水平的CD23。相比之下,用IL-4与GM-CSF或IL-3组合培养单核细胞会产生单一细胞群,这些细胞表达非常高水平的CD23。IL-4与GM-CSF或IL-3之间的协同作用也体现在可溶性CD23释放水平和CD23 mRNA表达水平上,并且在次优和最佳细胞因子浓度下均可见。GM-CSF、IL-3和IL-4均增强单核细胞II类主要组织相容性复合体(MHC)的表达,不过细胞因子组合未显示出相加或协同效应。单独作用时,IFN-γ未能诱导单核细胞CD23表达,不过在GM-CSF、IL-3或IL-4存在的情况下作用时,它会增强表面和可溶性CD23。相比之下,IFN-α是这三种细胞因子诱导的单核细胞CD23表达的强效抑制剂。(摘要截选至250字)

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