Post-transcriptional regulation of IL-6 production by Zc3h12a in fibroblast-like synovial cells

Clin Exp Rheumatol. 2011 Nov-Dec;29(6):906-12. Epub 2011 Dec 22.

Abstract

Objectives: Zc3h12a is an RNA binding protein with a CCCH-type finger motif and is known to regulate mRNA metabolism. Previous reports suggest that Zc3h12a acts as a negative regulator of inflammatory processes because it is involved in the degradation of IL-6 mRNA. We investigate the effect of Zc3h12a on IL-6 production in fibroblast-like synovial cells (FLS) from rheumatoid arthritis (RA) patients.

Methods: The expression of Zc3h12a in FLS was determined by polymerase chain reaction. To knock down Zc3h12a expression in FLS, siRNA for Zc3h12a was transfected by the lipofection method. The supernatants were collected after siRNA transfection for the quantification of IL-6 production. The phosphorylation of the signal transducer and activator of transcription 3 (STAT3) was examined by Western blotting. Cell proliferation was analysed by the Cell Counting Kit-8 assay after Zc3h12a knockdown.

Results: mRNA for Zc3h12a were demonstrated in FLS from RA patients. Zc3h12a transcripts were induced by LPS or IL-1β in FLS. The production of IL-6 as well as its mRNA expression was significantly increased by the Zc3h12a knockdown. The Zc3h12a knockdown also induced the activation of STAT3, which the anti IL-6 receptor antibody inhibited. Proliferation of Zc3h12a-knockdown FLS increased significantly in the presence of recombinant soluble IL-6 receptor (sIL-6R).

Conclusions: Our data suggest that Zc3h12a is a novel IL-6 regulator in FLS, which may be involved in the progression of RA.

MeSH terms

  • Arthritis, Rheumatoid / metabolism*
  • Arthritis, Rheumatoid / pathology
  • Arthritis, Rheumatoid / surgery
  • Cell Proliferation / drug effects
  • Cells, Cultured
  • Fibroblasts / drug effects
  • Fibroblasts / metabolism
  • Gene Expression Regulation*
  • Gene Knockdown Techniques
  • Gene Silencing
  • Humans
  • Interleukin-6 / genetics*
  • Interleukin-6 / metabolism
  • Interleukin-6 / pharmacology
  • Lipopolysaccharides / pharmacology
  • Phosphorylation
  • RNA, Small Interfering / genetics
  • RNA, Small Interfering / metabolism
  • Receptors, Interleukin-6 / antagonists & inhibitors
  • Receptors, Interleukin-6 / metabolism
  • Ribonucleases
  • STAT3 Transcription Factor / metabolism
  • Signal Transduction
  • Synovial Membrane / drug effects
  • Synovial Membrane / metabolism*
  • Synovial Membrane / pathology
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Transfection

Substances

  • Interleukin-6
  • Lipopolysaccharides
  • RNA, Small Interfering
  • Receptors, Interleukin-6
  • STAT3 Transcription Factor
  • Transcription Factors
  • Ribonucleases
  • ZC3H12A protein, human