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CD4+ T细胞上T1/ST2表达的调控及其功能:T1/ST2交联诱导2型细胞因子产生

Regulation and function of T1/ST2 expression on CD4+ T cells: induction of type 2 cytokine production by T1/ST2 cross-linking.

作者信息

Meisel C, Bonhagen K, Löhning M, Coyle A J, Gutierrez-Ramos J C, Radbruch A, Kamradt T

机构信息

Deutsches Rheumaforschungszentrum, Berlin, Germany.

出版信息

J Immunol. 2001 Mar 1;166(5):3143-50. doi: 10.4049/jimmunol.166.5.3143.

Abstract

The orphan receptor T1/ST2, a member of the IL-1R family, is preferentially expressed on the surface of murine Th2 cells. In this study, we analyzed the kinetics and function of T1/ST2 expression on Th2 cells in vitro. Whereas naive CD4(+) cells did not express T1/ST2, most CD4(+) cells became T1/ST2(+) upon repeated antigenic stimulation under Th2-polarizing conditions. Flow cytometric analyses revealed that the kinetics of T1/ST2 expression on Th2 cells was delayed compared with the kinetics of type 2 cytokine production. Exogenous IL-6, IL-5, IL-1, and TNF-alpha enhanced the expression of T1/ST2 on Th2 cells, and IL-6 was by far most effective in this regard. However, the expression of T1/ST2 did not depend on the presence of IL-6 and was also detected in IL-6-deficient mice. Most important, cross-linking of T1/ST2 provided a costimulatory signal for Th2 but not Th1 cells and directly induced proliferation and type 2 cytokine production. Thus, T1/ST2 is not only a Th2 cell marker but also plays an important role in the activation of Th2 cells.

摘要

孤儿受体T1/ST2是白细胞介素-1受体(IL-1R)家族的成员之一,在小鼠Th2细胞表面优先表达。在本研究中,我们分析了体外Th2细胞上T1/ST2表达的动力学和功能。初始CD4(+)细胞不表达T1/ST2,而在Th2极化条件下反复进行抗原刺激后,大多数CD4(+)细胞会变成T1/ST2(+)。流式细胞术分析显示,与2型细胞因子产生的动力学相比,Th2细胞上T1/ST2表达的动力学延迟。外源性白细胞介素-6(IL-6)、白细胞介素-5(IL-5)、白细胞介素-1(IL-1)和肿瘤坏死因子-α(TNF-α)可增强Th2细胞上T1/ST2的表达,其中IL-6在这方面最为有效。然而,T1/ST2的表达并不依赖于IL-6的存在,在IL-6缺陷小鼠中也能检测到。最重要的是,T1/ST2的交联为Th2细胞而非Th1细胞提供了共刺激信号,并直接诱导增殖和2型细胞因子产生。因此,T1/ST2不仅是Th2细胞的标志物,而且在Th2细胞的激活中也发挥着重要作用。

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