Morinobu A, Kumagai S, Yanagida H, Ota H, Ishida H, Matsui M, Yodoi J, Nakao K
Department of Medicine and Clinical Science, Kyoto University, Graduate School of Medicine, Japan.
J Clin Immunol. 1996 Nov;16(6):326-33. doi: 10.1007/BF01541668.
To examine a possible involvement of interleukin-10 (IL-10) in CD23/Fc epsilon RII expression in human monocytes, effects of IL-10 on the cell surface CD23 expression, soluble CD23 (sCD23) release, and CD23 type b mRNA expression were investigated. IL-10 suppressed IL-4-induced surface CD23 expression on monocytes in a dose-dependent manner, and this effect was completely neutralized by anti-IL-10 antibody. The suppressive effect of IL-10 on surface CD23 expression was not due to enhancement of sCD23 release from the cell surface because no increase in sCD23 in culture supernatant was detected after incubation with IL-10. Instead, the effect of IL-10 seemed to be exerted at the transcriptional level since IL-4-induced expression of CD23 type b mRNA was significantly reduced when IL-10 was present. Although IL-4 induced surface CD23 expression on both monocytes and B cells, the suppressive effect of IL-10 was observed only on monocytes, which underscores different regulatory mechanisms for CD23 expression between the two cell types.
为研究白细胞介素-10(IL-10)是否参与人单核细胞中CD23/FcεRII的表达,我们研究了IL-10对细胞表面CD23表达、可溶性CD23(sCD23)释放及CD23 b型mRNA表达的影响。IL-10以剂量依赖方式抑制IL-4诱导的单核细胞表面CD23表达,且该效应被抗IL-10抗体完全中和。IL-10对表面CD23表达的抑制作用并非由于细胞表面sCD23释放增加,因为与IL-10孵育后未检测到培养上清液中sCD23增加。相反,IL-10的作用似乎在转录水平发挥,因为存在IL-10时,IL-4诱导的CD23 b型mRNA表达显著降低。尽管IL-4诱导单核细胞和B细胞表面CD23表达,但IL-10的抑制作用仅在单核细胞中观察到,这突出了两种细胞类型之间CD23表达的不同调节机制。