Epithelial cells modulate genes associated with NF kappa B activation in co-cultured human macrophages
Language English Country Netherlands Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
R01 ES019325
NIEHS NIH HHS - United States
PubMed
21601940
PubMed Central
PMC4706171
DOI
10.1016/j.imbio.2011.04.009
PII: S0171-2985(11)00092-1
Knihovny.cz E-resources
- MeSH
- Cell Line MeSH
- Cytokines metabolism MeSH
- Epithelial Cells metabolism MeSH
- Coculture Techniques MeSH
- Humans MeSH
- Macrophages immunology metabolism MeSH
- RNA, Messenger genetics MeSH
- Intercellular Adhesion Molecule-1 genetics metabolism MeSH
- NF-kappa B antagonists & inhibitors metabolism MeSH
- Gene Expression Regulation * MeSH
- Respiratory Mucosa immunology metabolism MeSH
- Signal Transduction MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Cytokines MeSH
- RNA, Messenger MeSH
- Intercellular Adhesion Molecule-1 MeSH
- NF-kappa B MeSH
Macrophages located in airways and the alveolar space are continually exposed to different signals from the respiratory mucosa. In this respect, epithelial cells represent an important source of cytokines and mediators modulating the state of activation and/or differentiation of mononuclear phagocytes. Many of the proinflammatory genes induced in macrophages during immune and immunopathological reactions are regulated by transcription factor NF kappa B. The aim of our study was to characterize changes in the expression of genes associated with NF kappa B activation and signalling in THP-1 human macrophages co-cultured with A549 respiratory epithelial cells. At least 4-fold upregulation of mRNA level was found in 29 of 84 tested genes including genes for multiple cytokines and chemokines, membrane antigens and receptors, and molecules associated with NF kappa B signalling. The mRNA induction was confirmed at the level of protein expression by evaluating the release of IL-6 and IL-8 and by ICAM-1 expression. Blocking of one NFκB subunit by p65 siRNA inhibited the production of IL-6 in both cell types while IL-8 release from THP-1 cells did not seem to be affected. We conclude from our data that unstimulated respiratory epithelial cells regulate genes associated with NF kappa B dependent immune responses in human macrophages and that these interactions may play a key role in immediate responses in the respiratory mucosa.
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