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Cited by 831NF-κB Signaling PathwaysEstrogen and related hormone effectsGenomics and Chromatin Dynamics

The DOI matches its Crossref record; 81 of the 84 references it cites were found in a registry or an index, and 3 are not checked yet.

Characterization of Mechanisms Involved in Transrepression of NF-κB by Activated Glucocorticoid Receptors

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Scheinman, Robert I., Gualberto, Antonio, Jewell, Christine M., Cidlowski, John A., Baldwin, Albert S.·1995·Molecular and Cellular Biology
DOI 10.1128/mcb.15.2.943PMC PMC231982
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Abstract

Glucocorticoids are potent immunosuppressants which work in part by inhibiting cytokine gene transcription. We show here that NF-kappa B, an important regulator of numerous cytokine genes, is functionally inhibited by the synthetic glucocorticoid dexamethasone (DEX). In transfection experiments, DEX treatment in the presence of cotransfected glucocorticoid receptor (GR) inhibits NF-kappa B p65-mediated gene expression and p65 inhibits GR activation of a glucocorticoid response element. Evidence is presented for a direct interaction between GR and the NF-kappa B subunits p65 and p50. In addition, we demonstrate that the ability of p65, p50, and c-rel subunits to bind DNA is inhibited by DEX and GR. In HeLa cells, DEX activation of endogenous GR is sufficient to block tumor necrosis factor alpha or interleukin 1 activation of NF-kappa B at the levels of both DNA binding and transcriptional activation. DEX treatment of HeLa cells also results in a significant loss of nuclear p65 and a slight increase in cytoplasmic p65. These data reveal a second mechanism by which NF-kappa B activity may be regulated by DEX. We also report that RU486 treatment of wild-type GR and DEX treatment of a transactivation mutant of GR each can significantly inhibit p65 activity. In addition, we found that the zinc finger domain of GR is necessary for the inhibition of p65. This domain is also required for GR repression of AP-1. Surprisingly, while both AP-1 and NF-kappa B can be inhibited by activated GR, synergistic NF-kappa B/AP-1 activity is largely unaffected. These data suggest that NF-kappa B, AP-1, and GR interact in a complex regulatory network to modulate gene expression and that cross-coupling of NF-kappa B and GR plays an important role in glucocorticoid-mediated repression of cytokine transcription.

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Show all 82 references

Research works printed but not linked: 13

  1. Baeuerle, P. A., and D. Baltimore. 1991. The physiology of the NF-κB transcription factor. Hormonal control regulation of gene transcription. Mol. Aspects Cell. Regul. 6:409–432.
  2. 10.1128/mcb.11.10.4943-4951.1991 · DOI
  3. Beg, A. A., and A. S. Baldwin, Jr. 1994. Induction of multiple forms of NF-κB/rel by TNFα. Oncogene 9:1487–1492.
  4. 10.1128/mcb.13.6.3301-3310.1993 · DOI
  5. 10.1101/gad.6.10.1899 · DOI
  6. Culpepper, J., and F. Lee. 1987. Glucocorticoid regulation of lymphokine production by murine T lymphocytes. Lymphokines 13:275–289.
  7. 10.1128/mcb.2.9.1044-1051.1982 · DOI
  8. 10.1128/mcb.13.10.6231-6240.1993 · DOI · Paper page
  9. 10.1128/mcb.4.6.1172-1174.1984 · DOI
  10. 10.1128/mcb.13.6.3782-3791.1993 · DOI
  11. 10.1128/mcb.10.5.2327-2334.1990 · DOI
  12. 10.1128/mcb.10.3.1281-1286.1990 · DOI
  13. 10.1128/mcb.10.2.561-568.1990 · DOI · Paper page

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Metadata

Authors
Scheinman, R. I., Gualberto, A., Jewell, C. M., Cidlowski, J. A., & Baldwin, A. S.
Affiliations
University of North Carolina at Chapel Hill (US)
ORCID
Venue
Molecular and Cellular Biology
Publisher
Informa UK Limited
Published
1995-02
Volume
15
Issue
2
Pages
943-953
ISSN
  • 0270-7306 (ISSN-L)
  • 1098-5549
DOI
10.1128/mcb.15.2.943
PMC
PMC231982
OpenAlex
W2158110584
Cited by
819
References
82
Citations by year
2026: 12 · 2025: 9 · 2024: 2 · 2023: 6 · 2022: 6 · 2021: 10 · 2020: 11 · 2019: 8 · 2018: 17 · 2017: 12 · 2016: 16 · 2015: 16 · 2014: 17 · 2013: 25 · 2012: 19
FWCI
23.58
Type
journal article
Language
en
Open access
Licence
journals.asm.org/non-commercial-tdm-license (tdm)
Locations
  • Molecular and Cellular Biology (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › NF-κB Signaling Pathways
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Endocrinology › Estrogen and related hormone effects
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
Keywords
NF-κB, glucocorticoid receptor, dexamethasone, transrepression, NF-κB p65, P50, c-Rel, AP-1, cytokine gene transcription, zinc finger, transcriptional repression, TNF-α, interleukin-1, glucocorticoid response element, protein-protein interaction, immunosuppression
MeSH terms
Animals, Cell Line, Chlorocebus aethiops, Dexamethasone, Drug Synergism, Glutathione Transferase, HeLa Cells, Humans, Interleukin-1, Kinetics, Receptors, Glucocorticoid, Recombinant Fusion Proteins, Recombinant Proteins, Transfection, Tumor Necrosis Factor-alpha, Chloramphenicol O-Acetyltransferase, Mifepristone, Gene Expression, NF-kappa B, Transcription Factor AP-1, Macromolecular Substances, Transcription Factor RelA, NF-kappa B p50 Subunit

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