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白细胞介素-10抑制细胞表面CD23/IgE高亲和力受体II型的表达,不是通过增强可溶性CD23的释放,而是通过降低人单核细胞中CD23的信使核糖核酸表达。

IL-10 suppresses cell surface CD23/Fc epsilon RII expression, not by enhancing soluble CD23 release, but by reducing CD23 mRNA expression in human monocytes.

作者信息

Morinobu A, Kumagai S, Yanagida H, Ota H, Ishida H, Matsui M, Yodoi J, Nakao K

机构信息

Department of Medicine and Clinical Science, Kyoto University, Graduate School of Medicine, Japan.

出版信息

J Clin Immunol. 1996 Nov;16(6):326-33. doi: 10.1007/BF01541668.

Abstract

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.

摘要

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。

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