The Peptidylarginine Deiminase Inhibitor Cl-Amidine Suppresses Inducible Nitric Oxide Synthase Expression in Dendritic Cells

Int J Mol Sci. 2017 Oct 27;18(11):2258. doi: 10.3390/ijms18112258.


The conversion of peptidylarginine into peptidylcitrulline by calcium-dependent peptidylarginine deiminases (PADs) has been implicated in the pathogenesis of a number of diseases, identifying PADs as therapeutic targets for various diseases. The PAD inhibitor Cl-amidine ameliorates the disease course, severity, and clinical manifestation in multiple disease models, and it also modulates dendritic cell (DC) functions such as cytokine production, antigen presentation, and T cell proliferation. The beneficial effects of Cl-amidine make it an attractive compound for PAD-targeting therapeutic strategies in inflammatory diseases. Here, we found that Cl-amidine inhibited nitric oxide (NO) generation in a time- and dose-dependent manner in maturing DCs activated by lipopolysaccharide (LPS). This suppression of NO generation was independent of changes in NO synthase (NOS) enzyme activity levels but was instead dependent on changes in inducible NO synthase (iNOS) transcription and expression levels. Several upstream signaling pathways for iNOS expression, including the mitogen-activated protein kinase, nuclear factor-κB p65 (NF-κB p65), and hypoxia-inducible factor 1 pathways, were not affected by Cl-amidine. By contrast, the LPS-induced signal transducer and the activator of transcription (STAT) phosphorylation and activator protein-1 (AP-1) transcriptional activities (c-Fos, JunD, and phosphorylated c-Jun) were decreased in Cl-amidine-treated DCs. Inhibition of Janus kinase/STAT signaling dramatically suppressed iNOS expression and NO production, whereas AP-1 inhibition had no effect. These results indicate that Cl-amidine-inhibited STAT activation may suppress iNOS expression. Additionally, we found mildly reduced cyclooxygenase-2 expression and prostaglandin E2 production in Cl-amidine-treated DCs. Our findings indicate that Cl-amidine acts as a novel suppressor of iNOS expression, suggesting that Cl-amidine has the potential to ameliorate the effects of excessive iNOS/NO-linked immune responses.

Keywords: Cl-amidine; dendritic cells; inducible nitric oxide synthase; inflammatory diseases; peptidylarginine deiminase.

MeSH terms

  • Animals
  • Biomarkers
  • Cyclooxygenase 2 / genetics
  • Cyclooxygenase 2 / metabolism
  • Dendritic Cells / drug effects*
  • Dendritic Cells / immunology
  • Dendritic Cells / metabolism*
  • Dinoprostone / biosynthesis
  • Enzyme Activation / drug effects
  • Female
  • Gene Expression Regulation / drug effects*
  • Hypoxia-Inducible Factor 1, alpha Subunit / metabolism
  • Lipopolysaccharides / immunology
  • Mice
  • Nitric Oxide / metabolism
  • Nitric Oxide Synthase Type II / antagonists & inhibitors
  • Nitric Oxide Synthase Type II / genetics*
  • Nitric Oxide Synthase Type II / metabolism
  • Ornithine / analogs & derivatives*
  • Ornithine / pharmacology
  • STAT Transcription Factors / metabolism
  • Signal Transduction / drug effects
  • Transcription Factor AP-1 / metabolism
  • Transcription Factor RelA / metabolism


  • Biomarkers
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Lipopolysaccharides
  • N-alpha-benzoyl-N5-(2-chloro-1-iminoethyl)-L-ornithine amide
  • STAT Transcription Factors
  • Transcription Factor AP-1
  • Transcription Factor RelA
  • Nitric Oxide
  • Ornithine
  • Nitric Oxide Synthase Type II
  • Cyclooxygenase 2
  • Dinoprostone