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LPS and TNFα induce SOCS3 mRNA and inhibit IL‐6‐induced activation of STAT3 in macrophages
Abstract
Recent findings indicate that cytokine signaling can be modulated by other mediators of simultaneously activated signal transduction pathways. In this study we show that LPS and TNFα are potent inhibitors of IL‐6‐mediated STAT3 activation in human monocyte derived macrophages, rat liver macrophages and RAW 264.7 mouse macrophages but not in human hepatoma cells (HepG2) or in rat hepatocytes. Accordingly, LPS and TNFα were found to induce the expression of SOCS3 mRNA in each of the investigated type of macrophages but not in HepG2 cells. Using a specific inhibitor, evidence is presented that the p38 MAP kinase might be involved, especially for the inhibitory effect of TNFα.
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“Moreover, both hepatocytes in vivo and in culture respond to IL-6 treatment in a similar manner; that is, only STAT-3 homodimers (SIF A) are found (unpublished observations and ref. 30).”
From Expression of suppressors of cytokine signaling during liver regeneration (2001) · cites this paper as [30]
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“One notable exception is the human hepatoma cell line, HepG2 (Figure 1c), where SIF A, B (STAT-3:STAT-1), and C (STAT-1:STAT-1) DNA complexes are all detected after IL-6 treatment (30).”
From Expression of suppressors of cytokine signaling during liver regeneration (2001) · cites this paper as [30]
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Metadata
- Authors
- Bode, J. G., Nimmesgern, A., Schmitz, J., Schaper, F., Schmitt, M., Frisch, W., Häussinger, D., Heinrich, P. C., & Graeve, L.
- Affiliations
- Universitätsklinikum Aachen (DE)
- RWTH Aachen University (DE)
- Düsseldorf University Hospital (DE)
- Venue
- FEBS Letters
- Publisher
- Wiley
- Published
- 1999-12-17
- Volume
- 463
- Issue
- 3
- Pages
- 365-370
- ISSN
- 0014-5793 (ISSN-L)
- 1873-3468
- OpenAlex
- W2000974116
- Semantic Scholar
- 7c9e34a7b209b7772b86c66230245c02502400ce
- Cited by
- 196
- References
- 31
- Citations by year
- 2024: 6 · 2023: 2 · 2021: 3 · 2020: 8 · 2019: 5 · 2018: 2 · 2017: 7 · 2016: 6 · 2015: 5 · 2014: 10 · 2013: 6 · 2012: 13
- FWCI
- 3.58
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- FEBS Letters (publishedVersion)
- PubMed (publishedVersion)
- RWTH Publications (RWTH Aachen) (submittedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Cytokine Signaling Pathways and Interactions
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Tyrosine Phosphatases
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
- Keywords
- SOCS3, STAT3 activation, IL-6 signaling, lipopolysaccharide, TNF-α, macrophages, p38 MAPK, hepatic macrophages, hepatocytes
- MeSH terms
- Interleukin-6 Inhibitors, Animals, Cell Line, DNA-Binding Proteins, Gene Expression Regulation, Humans, Kupffer Cells, Lipopolysaccharides, Liver, Macrophages, Male, Tumor Cells, Cultured, Tumor Necrosis Factor-alpha, Signal Transduction, Trans-Activators, Genes, Suppressor, Rats, Wistar, Mitogen-Activated Protein Kinases, p38 Mitogen-Activated Protein Kinases, STAT3 Transcription Factor, Mice, Rats
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