Cited by 2,130Cytokine Signaling Pathways and InteractionsReceptor Mechanisms and SignalingProtein Tyrosine Phosphatases

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

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HEINRICH, Peter C., BEHRMANN, Iris, MÜLLER-NEWEN, Gerhard, SCHAPER, Fred, GRAEVE, Lutz·1998·Biochemical Journal

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.

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  • When IL-6 binds to its receptor complex composed of IL-6R and a gp130 homodimer, a cascade of signaling events is initiated, most notably the Jak/STAT pathway.

    “When IL-6 binds to its receptor complex composed of a specific receptor subunit, the IL-6 receptor (IL-6R), and a gp130 homo dimer, a cascade of signaling events is initiated, most notably the Jak/STAT pathway (14,15).”
  • IL-6 signalling through gp130 activates JAK and STAT, leading to expression of target genes such as SOCS3.

    “In both pathways, the activated IL‐6R‐gp130 complex binds and activates the Janus kinase (JAK) family of tyrosine kinases, primarily JAK1, JAK2, and TYK2, which phosphorylate the cytoplasmatic tail of gp130, enabling the association of the Signal Transducer and Activator of Transcription (STAT), mainly STAT1 and STAT3.”

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Authors
HEINRICH, P. C., BEHRMANN, I., MÜLLER-NEWEN, G., SCHAPER, F., & GRAEVE, L.
Affiliations
  • Universitätsklinikum Aachen (DE)
  • Institut für Biochemie, RWTH Aachen, Universitätsklinikum, Pauwelsstrasse 30, D-52057 Aachen, Germany
Venue
Biochemical Journal
Published
1998-09-01
Volume
334
Issue
2
Pages
297-314
ISSN
  • 0264-6021 (ISSN-L)
  • 1470-8728
OpenAlex
W1779691448
Cited by
2,130
References
225
Citations by year
2026: 40 · 2025: 46 · 2024: 49 · 2023: 47 · 2022: 59 · 2021: 59 · 2020: 64 · 2019: 80 · 2018: 58 · 2017: 87 · 2016: 94 · 2015: 79 · 2014: 66 · 2013: 100 · 2012: 93
FWCI
8.75
Type
journal article
Language
en
Open access
Locations
  • Biochemical Journal (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • Open Repository and Bibliography (University of Luxembourg) (submittedVersion)
Funders
Deutsche Forschungsgemeinschaft
Topics
  • Health Sciences › Medicine › Oncology › Cytokine Signaling Pathways and Interactions
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Tyrosine Phosphatases
Keywords
gp130, JAK/STAT signaling, Janus kinase, STAT1, STAT3, SHP2, receptor complex assembly, transcriptional activation, suppressor of cytokine signaling, PIAS, receptor internalization, interleukin-6, interleukin-11, leukemia inhibitory factor, oncostatin M, ciliary neurotrophic factor, cardiotrophin-1
MeSH terms
Animals, Cell Differentiation, Cell Division, Cell Membrane, Cell Nucleus, DNA-Binding Proteins, Gene Expression Regulation, Humans, Membrane Glycoproteins, Models, Molecular, Protein Conformation, Protein-Tyrosine Kinases, Signal Transduction, Transcriptional Activation, Trans-Activators, Antigens, CD, Interleukin-6, Cytokines, Receptors, Cytokine, Cytokine Receptor gp130

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