Enhanced AP-1 and NF-kappaB activities and stability of interleukin 8 (IL-8) transcripts are implicated in IL-8 mRNA superinduction in lung epithelial H292 cells

Détails

ID Serval
serval:BIB_F6185CFD417F
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Enhanced AP-1 and NF-kappaB activities and stability of interleukin 8 (IL-8) transcripts are implicated in IL-8 mRNA superinduction in lung epithelial H292 cells
Périodique
Biochemical Journal
Auteur(s)
Roger  T., Out  T., Mukaida  N., Matsushima  K., Jansen  H., Lutter  R.
ISSN
0264-6021 (Print)
Statut éditorial
Publié
Date de publication
02/1998
Volume
330
Numéro
1
Pages
429-435
Notes
Journal Article Research Support, Non-U.S. Gov't --- Old month value: Feb 15
Résumé
Inhibition of protein synthesis may result in superinduction of short-lived transcripts and has been attributed variably to stabilization of transcripts and/or increased gene transcription. Little is known about the kinetics of these processes and relevant transcriptional elements have not been identified. In this study, we describe superinduction of interleukin 8 (IL-8) mRNA, an important inflammatory mediator, in lung epithelial-like H292 cells and identify the underlying molecular mechanisms and their kinetics. Cycloheximide (CHI, 10 microg/ml), an inhibitor of protein synthesis, maximally increased IL-8 mRNA levels 30-fold in H292 cells. Tumour necrosis factor alpha (TNF-alpha), which induced IL-8 mRNA 3-fold, synergized with CHI causing a 150-fold increase at 6 h. CHI early on increased the stability of IL-8 mRNA (from 40 min in cells cultured with medium to more than 4 h with CHI). CHI also increased transcription as shown by transfection with IL-8 promoter constructs. Truncated and mutated constructs identified NF-kappaB and AP-1 binding sites as primary cis-acting elements in IL-8 gene transcription and IL-8 mRNA superinduction. Electrophoretic mobility shift assays indicated that CHI increased NF-kappaB and prolonged AP-1 DNA-binding activities and that the synergism of TNF-alpha and CHI on IL-8 mRNA expression was paralleled by a further increase of AP-1 DNA-binding activity. This synergism was still noticed when 4 h elapsed between the addition of CHI and that of TNF-alpha. Taken together, our results indicate that CHI interferes with both post-transcriptional and transcriptional repressive mechanisms of IL-8 mRNA expression.
Mots-clé
Cell Nucleus/metabolism Cycloheximide/pharmacology DNA-Binding Proteins/metabolism Epithelial Cells/metabolism Gene Expression Regulation Humans Interleukin-8/*physiology Lung/*physiology NF-kappa B/*metabolism Promoter Regions (Genetics) Protein Synthesis Inhibitors/pharmacology RNA, Messenger/metabolism RNA, Neoplasm/metabolism Transcription Factor AP-1/*metabolism Tumor Cells, Cultured Tumor Necrosis Factor-alpha/pharmacology
Pubmed
Web of science
Création de la notice
25/01/2008 14:35
Dernière modification de la notice
20/08/2019 17:22
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