Interactive effects of inflammatory cytokine and abundant low-molecular-weight PAHs on inhibition of gap junctional intercellular communication, disruption of cell proliferation control, and the AhR-dependent transcription
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
25268939
DOI
10.1016/j.toxlet.2014.09.023
PII: S0378-4274(14)01357-5
Knihovny.cz E-resources
- Keywords
- Aryl hydrocarbon receptor, Cell proliferation, Gap junctions, Inflammation, PAHs,
- MeSH
- Enzyme Activation MeSH
- Cell Line MeSH
- Time Factors MeSH
- Epithelial Cells drug effects metabolism pathology MeSH
- Fluorenes toxicity MeSH
- Transcription, Genetic drug effects MeSH
- Liver drug effects metabolism pathology MeSH
- Connexin 43 genetics metabolism MeSH
- Rats MeSH
- Gap Junctions drug effects metabolism pathology MeSH
- Cell Communication drug effects MeSH
- p38 Mitogen-Activated Protein Kinases metabolism MeSH
- Molecular Weight MeSH
- Cell Transformation, Neoplastic chemically induced metabolism pathology MeSH
- Liver Neoplasms chemically induced metabolism pathology MeSH
- Cell Proliferation drug effects MeSH
- Receptors, Aryl Hydrocarbon agonists genetics metabolism MeSH
- Gene Expression Regulation drug effects MeSH
- Signal Transduction drug effects MeSH
- Tumor Necrosis Factor-alpha toxicity MeSH
- Basic Helix-Loop-Helix Transcription Factors agonists genetics metabolism MeSH
- Dose-Response Relationship, Drug MeSH
- Inflammation chemically induced genetics metabolism pathology MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Ahr protein, rat MeSH Browser
- fluoranthene MeSH Browser
- Fluorenes MeSH
- Gja1 protein, rat MeSH Browser
- Connexin 43 MeSH
- p38 Mitogen-Activated Protein Kinases MeSH
- Receptors, Aryl Hydrocarbon MeSH
- Tumor Necrosis Factor-alpha MeSH
- Basic Helix-Loop-Helix Transcription Factors MeSH
Polycyclic aromatic hydrocarbons (PAHs) with lower molecular weight exhibit lesser genotoxicity and carcinogenicity than highly carcinogenic PAHs with a higher number of benzene rings. Nevertheless, they elicit specific effects linked with tumor promotion, such as acute inhibition of gap junctional intercellular communication (GJIC). Although inflammatory reaction may alter bioactivation and toxicity of carcinogenic PAHs, little is known about the impact of pro-inflammatory cytokines on toxic effects of the low-molecular-weight PAHs. Here, we investigated the impact of a pro-inflammatory cytokine, tumor necrosis factor-α (TNF-α), on the effects associated with tumor promotion and with induction of the aryl hydrocarbon receptor (AhR)-dependent gene expression in rat liver epithelial cells. We found that a prolonged incubation with TNF-α induced a down-regulation of GJIC, associated with reduced expression of connexin 43 (Cx43), a major connexin isoform found in liver epithelial cells. The Cx43 down-regulation was partly mediated by the activity of the mitogen-activated protein (MAP) p38 kinase. Independently of GJIC modulation, or p38 activation, TNF-α potentiated the AhR-dependent proliferative effect of a model low-molecular-weight PAH, fluoranthene, on contact-inhibited cells. In contrast, this pro-inflammatory cytokine repressed the fluoranthene-induced expression of a majority of model AhR gene targets, such as Cyp1a1, Ahrr or Tiparp. The results of the present study indicate that inflammatory reaction may differentially modulate various toxic effects of low-molecular-weight PAHs; the exposure to pro-inflammatory cytokines may both strengthen (inhibition of GJIC, disruption of contact inhibition) and repress (expression of a majority of AhR-dependent genes) their impact on toxic endpoints associated with carcinogenesis.
Department of Cytokinetics Institute of Biophysics AS CR Královopolská 135 61265 Brno Czech Republic
References provided by Crossref.org
Applicability of Scrape Loading-Dye Transfer Assay for Non-Genotoxic Carcinogen Testing