te Velde A A, Huijbens R J, de Vries J E, Figdor C G
Division of Immunology, The Netherlands Cancer Institute, Amsterdam.
J Immunol. 1990 Apr 15;144(8):3046-51.
Monocytes can express three classes of FcR for IgG: Fc gamma RI, Fc gamma RII, and Fc gamma RIII (CD64, CD32, and CD16, respectively) of which the Fc gamma RIII is expressed after prolonged culture. Fc gamma R expression is regulated by IFN-gamma. Because IFN-gamma and IL-4 have antagonistic effects on the expression of the FcR for IgE on human monocytes, we studied the effect of IL-4 on Fc gamma R expression and function. We show that IL-4 down-regulates Fc gamma RI, Fc gamma RII, and Fc gamma RIII expression of cultured monocytes and inhibits IFN-gamma enhanced Fc gamma RI expression. Exposure of monocytes to IL-4 for 40 h resulted in a dose-dependent decrease of the expression of all three Fc gamma R that persisted throughout the whole culture period (7 days). Anti-IL-4 antibodies completely reversed the IL-4 effect. In addition the impaired Fc gamma R expression correlated directly with reduced Fc gamma R-mediated function because monocytes cultured in the presence of IL-4 have a reduced capacity to lyse human E opsonized with human IgG anti-D or mouse antiglycophorin A antibodies. These observations, together with the previous finding that IL-4 induces Fc epsilon RIIb expression on monocytes, indicate that IL-4 and IFN-gamma may control the Fc gamma R-mediated immune response by differentially regulating Fc gamma R expression.
单核细胞可表达三类针对IgG的Fc受体:FcγRI、FcγRII和FcγRIII(分别为CD64、CD32和CD16),其中FcγRIII在长时间培养后表达。FcγR的表达受干扰素-γ调控。由于干扰素-γ和白细胞介素-4对人单核细胞上IgE的Fc受体表达具有拮抗作用,我们研究了白细胞介素-4对FcγR表达及功能的影响。我们发现白细胞介素-4可下调培养的单核细胞中FcγRI、FcγRII和FcγRIII的表达,并抑制干扰素-γ增强的FcγRI表达。单核细胞暴露于白细胞介素-4 40小时导致所有三种FcγR的表达呈剂量依赖性下降,且在整个培养期(7天)持续存在。抗白细胞介素-4抗体可完全逆转白细胞介素-4的作用。此外,FcγR表达受损与FcγR介导的功能降低直接相关,因为在白细胞介素-4存在下培养的单核细胞对用人IgG抗-D或小鼠抗血型糖蛋白A抗体致敏的人红细胞的裂解能力降低。这些观察结果,连同先前发现白细胞介素-4可诱导单核细胞上FcεRIIb表达,表明白细胞介素-4和干扰素-γ可能通过差异调节FcγR表达来控制FcγR介导的免疫反应。