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通过gp130/Jak/STAT途径的白细胞介素-6型细胞因子信号传导。

Interleukin-6-type cytokine signalling through the gp130/Jak/STAT pathway.

作者信息

Heinrich P C, Behrmann I, Müller-Newen G, Schaper F, Graeve L

机构信息

Institut für Biochemie, RWTH Aachen, Universitätsklinikum, Pauwelsstrasse 30, D-52057 Aachen, Germany.

出版信息

Biochem J. 1998 Sep 1;334 ( Pt 2)(Pt 2):297-314. doi: 10.1042/bj3340297.

Abstract

The family of cytokines signalling through the common receptor subunit gp130 comprises interleukin (IL)-6, IL-11, leukaemia inhibitory factor, oncostatin M, ciliary neurotrophic factor and cardiotrophin-1. These so-called IL-6-type cytokines play an important role in the regulation of complex cellular processes such as gene activation, proliferation and differentiation. The current knowledge on the signal-transduction mechanisms of these cytokines from the plasma membrane to the nucleus is reviewed. In particular, we focus on the assembly of receptor complexes after ligand binding, the activation of receptor-associated kinases of the Janus family, and the recruitment and phosphorylation of transcription factors of the STAT family, which dimerize, translocate to the nucleus, and bind to enhancer elements of respective target genes leading to transcriptional activation. The important players in the signalling pathway, namely the cytokines and the receptor components, the Janus kinases Jak1, Jak2 and Tyk2, the signal transducers and activators of transcription STAT1 and STAT3 and the tyrosine phosphatase SHP2 [SH2 (Src homology 2) domain-containing tyrosine phosphatase] are introduced and their structural/functional properties are discussed. Furthermore, we review various mechanisms involved in the termination of the IL-6-type cytokine signalling, namely the action of tyrosine phosphatases, proteasome, Jak kinase inhibitors SOCS (suppressor of cytokine signalling), protein inhibitors of activated STATs (PIAS), and internalization of the cytokine receptors via gp130. Although all IL-6-type cytokines signal through the gp130/Jak/STAT pathway, the comparison of their physiological properties shows that they elicit not only similar, but also distinct, biological responses. This is reflected in the different phenotypes of IL-6-type-cytokine knock-out animals.

摘要

通过共同受体亚基gp130发出信号的细胞因子家族包括白细胞介素(IL)-6、IL-11、白血病抑制因子、制瘤素M、睫状神经营养因子和心肌营养素-1。这些所谓的IL-6型细胞因子在调节复杂的细胞过程如基因激活、增殖和分化中发挥重要作用。本文综述了目前关于这些细胞因子从质膜到细胞核的信号转导机制的知识。特别地,我们关注配体结合后受体复合物的组装、Janus家族受体相关激酶的激活以及STAT家族转录因子的募集和磷酸化,这些转录因子二聚化、转运到细胞核并结合到各自靶基因的增强子元件上从而导致转录激活。介绍了信号通路中的重要参与者,即细胞因子和受体成分、Janus激酶Jak1、Jak2和Tyk2、信号转导和转录激活因子STAT1和STAT3以及含SH2(Src同源2)结构域的酪氨酸磷酸酶SHP2,并讨论了它们的结构/功能特性。此外,我们还综述了参与IL-6型细胞因子信号终止的各种机制,即酪氨酸磷酸酶、蛋白酶体、Jak激酶抑制剂细胞因子信号抑制因子(SOCS)、活化STAT蛋白抑制剂(PIAS)的作用以及细胞因子受体通过gp130的内化。尽管所有IL-6型细胞因子都通过gp130/Jak/STAT途径发出信号,但对它们生理特性的比较表明,它们不仅引发相似的,而且还引发不同的生物学反应。这在IL-6型细胞因子基因敲除动物的不同表型中得到体现。

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