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Glucocorticoids suppress NF-kappaB activation induced by LPS and PGN in paranasal sinus epithelial cells. | LitMetric

Glucocorticoids suppress NF-kappaB activation induced by LPS and PGN in paranasal sinus epithelial cells.

Rhinology

Department of Otorhinolaryngology and Head and Neck Surgery, Division of Clinical Medical Science, Programs for Applied Biomedicine, Graduate School of Biomedical Science, Hiroshima University, Minami-ku, Hiroshima, Japan.

Published: December 2009

AI Article Synopsis

  • * Researchers measured the p50 levels as an indicator of the immune response after stimulating the cells with lipopolysaccharide (LPS) and peptidoglycan (PGN), and found that GCs like dexamethasone (DEX) could suppress this response.
  • * Results indicated that TLR2 and TLR4 are activated during immune responses, leading to increased inflammation, but GCs not only reduce inflammation but may also enhance the body's innate defenses against pathogens.

Article Abstract

Objectives: The aim of this study was to examine the innate immune response induced by toll-like receptors (TLRs) in the paranasal sinus epithelial cells in cell culture models and to examine the effect of glucocorticoids (GCs) on the innate immune response.

Methods: After stimulation with lipopolysaccharide (LPS) and peptidoglycan (PGN), p50 level was measured as an index of the innate response in the paranasal sinus epithelium. To observe the effect of GCs, the specimens were pre-treated with dexamethasone (DEX) for 48 hours prior to stimulation. On immunocytochemistry GR, TLR2 and TLR4 in the paranasal sinus epithelium were observed.

Results: The p50 activity levels increased after stimulation with LPS and PGN in a dose-dependent manner. Pretreatment with DEX significantly suppressed the increase in p50 activity levels induced by LPS and PGN. On immunocytochemistry, TLR2 and TLR4 immunoreactivities were relatively high after 48h DEX pretreatment.

Conclusion: The increase in NF-kappaB activity after LPS and PGN stimulation suggests that stimulation through TLR2 and TLR4 may induce high cytokine expression and inflammatory cell migration in the paranasal sinus epithelial cells. In paranasal sinus epithelial cells GCs not only have anti-inflammatory effects through transcription factor inhibition but also enhance innate host defences.

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Source
http://dx.doi.org/10.4193/Rhin08.074DOI Listing

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