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白细胞介素-6通过白细胞介素-2依赖和非依赖机制促进新鲜分离的人T细胞产生白细胞介素-4和白细胞介素-5。

Interleukin-6 promotes the production of interleukin-4 and interleukin-5 by interleukin-2-dependent and -independent mechanisms in freshly isolated human T cells.

作者信息

Heijink Irene H, Vellenga Edo, Borger Peter, Postma Dirkje S, de Monchy Jan G R, Kauffman Henk F

机构信息

Department of Allergology, University Hospital Groningen, Hanzeplein 1, NL-9713 GZ Groningen, the Netherlands.

出版信息

Immunology. 2002 Nov;107(3):316-24. doi: 10.1046/j.1365-2567.2002.01501.x.

Abstract

T helper 2 (Th2) cytokines [interleukin (IL)-4 and IL-5] play a central role in the development of allergic immune responses. After allergen provocation, the expression of Th2 cytokines is rapidly up-regulated in atopy and asthma. IL-6 is a multifunctional cytokine that is able to direct Th2 immune responses and is secreted by multiple tissue cell types. This study shows that IL-6 induces up-regulation of IL-4 and IL-5 after short (5 min) preincubation periods in freshly isolated, alpha-CD3/alpha-CD28-stimulated T cells. After longer preincubation periods with IL-6 (12 and 24 hr), the priming effect on IL-4 production gradually disappears, whereas the effect on IL-5 becomes more pronounced. In contrast, a small but significant inhibitory effect is found on the production of the Th1 cytokine interferon-gamma. Additional experiments indicate that the long-term priming effect of IL-6 on IL-5 production is dependent on IL-2 signalling. This is not the case for the short-term IL-6 effect on IL-5 secretion, where the p38 mitogen-activated protein kinase-dependent induction of activator protein-1 DNA-binding activity is involved, independent of signal transducer and activator of transcription 3 phosphorylation. In summary, these data demonstrate that the short-term and long-term priming effects of IL-6 on Th2 cytokine production are regulated by different mechanisms.

摘要

辅助性T细胞2(Th2)细胞因子[白细胞介素(IL)-4和IL-5]在过敏性免疫反应的发展中起核心作用。变应原激发后,Th2细胞因子的表达在特应性疾病和哮喘中迅速上调。IL-6是一种多功能细胞因子,能够指导Th2免疫反应,由多种组织细胞类型分泌。本研究表明,在新鲜分离的、α-CD3/α-CD28刺激的T细胞中,短时间(5分钟)预孵育后,IL-6可诱导IL-4和IL-5上调。用IL-6预孵育较长时间(12小时和24小时)后,对IL-4产生的启动作用逐渐消失,而对IL-5的作用则变得更加明显。相反,发现对Th1细胞因子干扰素-γ的产生有轻微但显著的抑制作用。额外的实验表明,IL-6对IL-5产生的长期启动作用依赖于IL-2信号传导。对于IL-6对IL-5分泌的短期作用则并非如此,其中涉及p38丝裂原活化蛋白激酶依赖性诱导激活蛋白-1 DNA结合活性,与信号转导子和转录激活子3磷酸化无关。总之,这些数据表明,IL-6对Th2细胞因子产生的短期和长期启动作用受不同机制调控。

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