Abstract
The inhibitory effect of interleukin-10 (IL-10), an anti-inflammatory cytokine, on lipopolysaccharide (LPS)-induced IL-6 production was characterized by simultaneous stimulation of RAW 264.7 cells with LPS and IL-10. The presence of IL-10 significantly inhibited LPS-induced IL-6 production at a transcriptional level. The expression of IκB-ζ, which promotes IL-6 production, was induced in response to LPS and it was definitely suppressed in the presence of IL-10. Further, IL-10 inhibited LPS-induced NF-κB activation. A pharmacological inhibitor of NF-κB prevented LPS-induced IκB-ζ expression, suggesting that IL-10 might inhibit LPS-induced IκB-ζ expression via the inactivation of NF-κB. In LPS- and IL-10-stimulated cells, the expression of Bcl-3 that inhibits NF-κB activation was significantly augmented. Introduction of Bcl-3 siRNA abolished IL-10-mediated IκB-ζ inhibition. In the presence of Bcl-3, siRNA IL-10 failed to inhibit LPS-induced IL-6 production. Therefore, it was suggested that Bcl-3 induced by IL-10 might reduce LPS-induced IκB-ζ activity via inactivation of NF-κB and that reduced IκB-ζ activity failed to promote LPS-induced IL-6 production.
| Original language | English |
|---|---|
| Pages (from-to) | 217-224 |
| Number of pages | 8 |
| Journal | Innate Immunity |
| Volume | 15 |
| Issue number | 4 |
| DOIs | |
| Publication status | Published - 2009 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
All Science Journal Classification (ASJC) codes
- Microbiology
- Immunology
- Molecular Biology
- Cell Biology
- Infectious Diseases
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