Casuarinin suppresses TARC/CCL17 and MDC/CCL22 production via blockade of NF-κB and STAT1 activation in HaCaT cells

Biochem Biophys Res Commun. 2012 Jan 27;417(4):1254-9. doi: 10.1016/j.bbrc.2011.12.119. Epub 2011 Dec 29.

Abstract

Casuarinin is a naturally occurring tannin that is isolated from the leaves of Hippophae rhamnoides. It has been shown to have anti-oxidant, anti-cancer, anti-viral, and anti-inflammatory activities. The aim of this study was to investigate the possible mechanism by which casuarinin inhibits TNF-α/IFN-γ-induced Th2 chemokines expression in the human keratinocytes cell line HaCaT. We found that casuarinin suppressed TNF-α/IFN-γ-induced expression of TARC and MDC mRNA and protein in HaCaT cells. Casuarinin significantly inhibited TNF-α/IFN-γ-induced activation of NF-κB, STAT1, and p38 MAPK. Furthermore, we observed that p38 MAPK contributes to inhibition of TNF-α/IFN-γ-induced TARC and MDC production by blocking NF-κB and STAT1 activation in HaCaT cells. Taken together, these results suggest that casuarinin may exert anti-inflammatory responses by suppressing TNF-α/IFN-γ-induced expression of TARC and MDC via blockage of p38 MAPK activation and subsequent activation of NF-κB and STAT1. We propose that it could therefore be used as a therapeutic agent against inflammatory skin diseases.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / pharmacology*
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use
  • Cell Line
  • Chemokine CCL17 / antagonists & inhibitors*
  • Chemokine CCL17 / biosynthesis
  • Chemokine CCL22 / antagonists & inhibitors*
  • Chemokine CCL22 / biosynthesis
  • Dermatitis / drug therapy
  • Humans
  • Hydrolyzable Tannins / pharmacology*
  • Hydrolyzable Tannins / therapeutic use
  • Interferon-gamma / pharmacology
  • Keratinocytes / drug effects
  • Keratinocytes / metabolism
  • NF-kappa B / antagonists & inhibitors*
  • STAT1 Transcription Factor / antagonists & inhibitors*
  • Tumor Necrosis Factor-alpha / pharmacology
  • p38 Mitogen-Activated Protein Kinases / metabolism

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Chemokine CCL17
  • Chemokine CCL22
  • Hydrolyzable Tannins
  • NF-kappa B
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • Tumor Necrosis Factor-alpha
  • casuarinin
  • Interferon-gamma
  • p38 Mitogen-Activated Protein Kinases