Interleukin (IL)-10 attenuates lipopolysaccharide-induced IL-6 production via inhibition of IκB-ζ activity by Bcl-3

Jargalsaikhan Dagvadorj, Yoshikazu Naiki, Gantsetseg Tumurkhuu, Abu Shadat Mohammod Noman, Imtiaz Iftekar-E-Khuda, Naoki Koide, Takayuki Komatsu, Tomoaki Yoshida, Takashi Yokochi

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16 Citations (Scopus)


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 languageEnglish
Pages (from-to)217-224
Number of pages8
JournalInnate Immunity
Issue number4
Publication statusPublished - 2009

All Science Journal Classification (ASJC) codes

  • Microbiology
  • Immunology
  • Molecular Biology
  • Cell Biology
  • Infectious Diseases


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