te Velde A A, Rousset F, Peronne C, De Vries J E, Figdor C G
Division of Immunology, The Netherlands Cancer Institute, Amsterdam.
J Immunol. 1990 Apr 15;144(8):3052-9.
We used highly purified human monocytes to study the regulation of cell surface and secretion of the low affinity FcR for IgE (Fc epsilon RIIb). IL-4 induces Fc epsilon RIIb expression and soluble Fc epsilon RIIb release in a dose-dependent manner. Significant levels of Fc epsilon RIIb expression were obtained after 12 h of incubation with IL-4 and maximal expression was observed between 24 to 48 h after which the expression declined. Surface expression was followed by secretion of soluble Fc epsilon RIIb which reached maximal levels after 3 to 4 days of incubation and which remained constant throughout 7 days of culture. Induction of Fc epsilon RIIb expression by IL-4 was completely blocked by anti-IL-4 antibodies. Furthermore, IL-1 alpha, IL-2, IL-5, granulocyte-macrophage-CSF, IFN-alpha, IFN-gamma, low m.w. BCGF and also LPS all failed to induce Fc epsilon RIIb expression, demonstrating the specificity of the induction. Fc epsilon RIIb membrane expression induced by IL-4 was reduced in the presence of IFN-gamma and IFN-alpha. Strong inhibition of IL-4-induced Fc epsilon RIIb expression was observed at IFN-alpha concentrations of 450 U/ml (80%), and 100 U/ml of IFN-gamma reduced IL-4-induced Fc epsilon RIIb expression by 70%. Interestingly, soluble Fc epsilon RIIb release was strongly inhibited by IFN-alpha. In contrast, IFN-gamma did not affect soluble Fc epsilon RIIb release, suggesting that reduced membrane expression of Fc epsilon RIIb observed in the presence of IFN-gamma does not reflect inhibition of Fc epsilon RIIb expression but may represent enhanced cleavage or reduced anchoring in the membrane of Fc epsilon RIIb. Finally, IL-5 that has been shown to enhance IL-4-induced Fc epsilon RII on B cells does not enhance significantly IL-4-induced Fc epsilon RIIb membrane expression or subsequent soluble Fc epsilon RIIb release by monocytes. Taken together these results show that IFN-alpha and IFN-gamma have different regulatory effects on IL-4-induced Fc epsilon RIIb membrane expression and soluble Fc epsilon RIIb release by human monocytes.
我们使用高度纯化的人单核细胞来研究细胞表面免疫球蛋白E低亲和力Fc受体(FcεRIIb)的调节及其分泌情况。白细胞介素-4(IL-4)以剂量依赖的方式诱导FcεRIIb的表达及可溶性FcεRIIb的释放。与IL-4孵育12小时后可获得显著水平的FcεRIIb表达,在24至48小时之间观察到最大表达,之后表达下降。表面表达之后是可溶性FcεRIIb的分泌,在孵育3至4天后达到最大水平,并在整个7天的培养过程中保持恒定。抗IL-4抗体可完全阻断IL-4对FcεRIIb表达的诱导。此外,IL-1α、IL-2、IL-5、粒细胞-巨噬细胞集落刺激因子(GM-CSF)、干扰素-α(IFN-α)、干扰素-γ(IFN-γ)、低分子量B细胞生长因子(BCGF)以及脂多糖(LPS)均未能诱导FcεRIIb表达,这证明了诱导的特异性。在IFN-γ和IFN-α存在的情况下,IL-4诱导的FcεRIIb膜表达降低。在IFN-α浓度为450 U/ml时可观察到对IL-4诱导的FcεRIIb表达的强烈抑制(80%),1百U/ml的IFN-γ可使IL-4诱导的FcεRIIb表达降低70%。有趣的是,IFN-α强烈抑制可溶性FcεRIIb的释放。相反,IFN-γ不影响可溶性FcεRIIb的释放,这表明在IFN-γ存在下观察到的FcεRIIb膜表达降低并非反映对FcεRIIb表达的抑制,而可能代表FcεRIIb在膜中的切割增强或锚定减少。最后,已证明可增强B细胞上IL-4诱导的FcεRII的IL-5,对单核细胞中IL-4诱导的FcεRIIb膜表达或随后的可溶性FcεRIIb释放并无显著增强作用。综上所述,这些结果表明IFN-α和IFN-γ对人单核细胞中IL-4诱导的FcεRIIb膜表达和可溶性FcεRIIb释放具有不同的调节作用。