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白细胞介素(IL)-6 型细胞因子信号传导原理及其调控

Principles of interleukin (IL)-6-type cytokine signalling and its regulation.

作者信息

Heinrich Peter C, Behrmann Iris, Haan Serge, Hermanns Heike M, Müller-Newen Gerhard, Schaper Fred

机构信息

Institut für Biochemie, RWTH Aachen, Universitätsklinikum, Pauwelsstrasse 30, D-52074 Aachen, Germany.

出版信息

Biochem J. 2003 Aug 15;374(Pt 1):1-20. doi: 10.1042/BJ20030407.

DOI:10.1042/BJ20030407
PMID:12773095
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1223585/
Abstract

The IL (interleukin)-6-type cytokines IL-6, IL-11, LIF (leukaemia inhibitory factor), OSM (oncostatin M), ciliary neurotrophic factor, cardiotrophin-1 and cardiotrophin-like cytokine are an important family of mediators involved in the regulation of the acute-phase response to injury and infection. Besides their functions in inflammation and the immune response, these cytokines play also a crucial role in haematopoiesis, liver and neuronal regeneration, embryonal development and fertility. Dysregulation of IL-6-type cytokine signalling contributes to the onset and maintenance of several diseases, such as rheumatoid arthritis, inflammatory bowel disease, osteoporosis, multiple sclerosis and various types of cancer (e.g. multiple myeloma and prostate cancer). IL-6-type cytokines exert their action via the signal transducers gp (glycoprotein) 130, LIF receptor and OSM receptor leading to the activation of the JAK/STAT (Janus kinase/signal transducer and activator of transcription) and MAPK (mitogen-activated protein kinase) cascades. This review focuses on recent progress in the understanding of the molecular mechanisms of IL-6-type cytokine signal transduction. Emphasis is put on the termination and modulation of the JAK/STAT signalling pathway mediated by tyrosine phosphatases, the SOCS (suppressor of cytokine signalling) feedback inhibitors and PIAS (protein inhibitor of activated STAT) proteins. Also the cross-talk between the JAK/STAT pathway with other signalling cascades is discussed.

摘要

白细胞介素(IL)-6 型细胞因子,包括 IL-6、IL-11、白血病抑制因子(LIF)、抑瘤素 M(OSM)、睫状神经营养因子、心肌营养素-1 和心肌营养素样细胞因子,是参与调节对损伤和感染的急性期反应的重要介质家族。除了在炎症和免疫反应中的作用外,这些细胞因子在造血、肝脏和神经元再生、胚胎发育及生育能力方面也发挥着关键作用。IL-6 型细胞因子信号传导失调会导致多种疾病的发生和维持,如类风湿性关节炎、炎症性肠病、骨质疏松症、多发性硬化症以及各种类型的癌症(如多发性骨髓瘤和前列腺癌)。IL-6 型细胞因子通过信号转导分子糖蛋白(gp)130、LIF 受体和 OSM 受体发挥作用,从而激活 JAK/STAT(Janus 激酶/信号转导子和转录激活子)和 MAPK(丝裂原活化蛋白激酶)级联反应。本综述着重阐述了对 IL-6 型细胞因子信号转导分子机制理解的最新进展。重点关注由酪氨酸磷酸酶、细胞因子信号传导抑制因子(SOCS)反馈抑制剂和 STAT 激活蛋白抑制剂(PIAS)蛋白介导的 JAK/STAT 信号通路的终止和调节作用。同时也讨论了 JAK/STAT 通路与其他信号级联反应之间的相互作用。

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Essential role of caveolae in interleukin-6- and insulin-like growth factor I-triggered Akt-1-mediated survival of multiple myeloma cells.小窝在白细胞介素-6和胰岛素样生长因子I触发的Akt-1介导的多发性骨髓瘤细胞存活中的重要作用。
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Akt modulates STAT3-mediated gene expression through a FKHR (FOXO1a)-dependent mechanism.Akt通过一种依赖FKHR(FOXO1a)的机制调节STAT3介导的基因表达。
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