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Biochem Biophys Res Commun. 2000 Jul 14;273(3):1008-14.

Glucocorticoid effects on NF-kappaB binding in the transcription of the ICAM-1 gene.

Author information

1
Department of Medical Nutrition, Karolinska Institute, Huddinge University Hospital, Novum F60, Huddinge, S-141 86, Sweden. Johan.Liden@mednut.ki.se

Abstract

Glucocorticoid hormones are potent antiinflammatory drugs. A key mechanism in the antiinflammatory action is repression of the nuclear factor kappa B (NF-kappaB) signaling pathway. This results in transcriptional repression of inflammatory genes controlled by NF-kappaB, including the intercellular adhesion molecule-1 (ICAM-1). We have investigated expression levels, nuclear translocation and DNA binding of NF-kappaB in vitro and in vivo in U937 cells during activation and repression. Repression of NF-kappaB signaling by glucocorticoids does not prevent NF-kappaB translocation or DNA binding. However interestingly, in vivo foot printing of the NF-kappaB site in the ICAM-1 gene indicates that glucocorticoids change the conformation of the protein complex binding to the NF-kappaB site. These results suggests that NF-kappaB interaction with the glucocorticoid receptor does not displace NF-kappaB from its DNA binding site but rather changes the complex into a transcriptionally inert form.

PMID:
10891363
DOI:
10.1006/bbrc.2000.3079
[Indexed for MEDLINE]

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