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PMID: 9716487 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

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

The Biochemical journal ·Vol. 334 ( Pt 2) ·1998-09-01 ·Pages 297-314

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

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.

MeSH Terms
Animals Antigens, CD/metabolism Cell Differentiation Cell Division Cell Membrane/metabolism Cell Nucleus/metabolism Cytokine Receptor gp130 Cytokines/chemistry,physiology DNA-Binding Proteins/metabolism Gene Expression Regulation Humans Interleukin-6/physiology Membrane Glycoproteins/metabolism Models, Molecular Protein Conformation Protein-Tyrosine Kinases/metabolism Receptors, Cytokine/chemistry,physiology Signal Transduction Trans-Activators/metabolism Transcriptional Activation
Chemicals
Antigens, CD Cytokines DNA-Binding Proteins IL6ST protein, human Interleukin-6 Membrane Glycoproteins Receptors, Cytokine Trans-Activators Cytokine Receptor gp130 Protein-Tyrosine Kinases
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Heinrich P C
Institut für Biochemie, RWTH Aachen, Universitätsklinikum, Pauwelsstrasse 30, D-52057 Aachen, Germany. [email protected]
Behrmann I
Müller-Newen G
Schaper F
Graeve L
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Article Info
Journal
The Biochemical journal
Abbr.
Biochem J
ISSN
0264-6021
Published
1998-09-01
Pages
297-314
Language
English
Region
England
NLM ID
2984726R
PMCID
PMC1219691
Subset
IM
Analysis Services
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