Evidence map›Paper›PMID 8612579›Full record

ArticleThe EMBO journal1996

Differentiation and growth arrest signals are generated through the cytoplasmic region of gp130 that is essential for Stat3 activation.

Y Yamanaka, K Nakajima, T Fukada, M Hibi, T Hirano

Abstract read
In one paragraph

Article in The EMBO journal, 1996. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

63 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. IL-6 in inflammation, autoimmunity and cancer.International immunology · 2021
    Review
  6. Article
  7. Article
  8. Molecules (Basel, Switzerland) · 2020
    Article
  9. Article
  10. Article
  11. Smad7 enables STAT3 activation and promotes pluripotency independent of TGF-β signaling.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  12. Article
  13. Review
  14. Article
  15. TGR5, Not Only a Metabolic Regulator.Frontiers in physiology · 2016
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Article

3 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Y YamanakaDepartment of Molecular Oncology, Osaka University Medical School, Japan.
K Nakajima
T Fukada
M Hibi
T Hirano

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin-6 (IL-6) induces growth arrest and macrophage differentiation through its receptor in a murine myeloid leukaemic cell line, M1, although it is largely unknown how the IL-6 receptor generates these signals. By using chimeric receptors consisting of the extracellular domain of growth hormone receptor and the transmembrane and cytoplasmic domain of gp130 with progressive C-terminal truncations, we showed that the membrane-proximal 133, but not 108, amino acids of gp130 could generate the signals for growth arrest, macrophage differentiation, down-regulation of c-myc and c-myb, induction of junB and IRF1 and Stat3 activation. Mutational analysis of this region showed that the tyrosine residue with the YXXQ motif was critical not only for Stat3 activation but also for growth arrest and differentiation, accompanied by down-regulation of c-myc and c-myb and immediate early induction of junB and IRF1. The tight correlation between Stat3 activation and other IL-6 functions was further observed in the context of the full-length cytoplasmic region of gp130. The result suggest that Stat3 plays an essential role in the signals for growth arrest and differentiation.

Indexed as

Amino Acid SequenceAnimalsAntigens, CDCell DifferentiationCell DivisionCell LineCytokine Receptor gp130CytoplasmDNA-Binding ProteinsGene Expression RegulationInterleukin-6Membrane GlycoproteinsMiceMolecular Sequence DataMolecular StructureRecombinant Fusion ProteinsAntigens, CDCytokine Receptor gp130DNA-Binding ProteinsIl6st protein, mouseInterleukin-6Membrane GlycoproteinsRecombinant Fusion ProteinsStat3 protein, mouseSTAT3 Transcription FactorTrans-ActivatorsTyrosine

Identifiers

PMID8612579
PMCPMC450065

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.