Semi-vioxanthin isolated from marine-derived fungus regulates tumor necrosis factor-alpha, cluster of differentiation (CD) 80, CD86, and major histocompatibility complex class II expression in RAW264.7 cells via nuclear factor-kappaB and mitogen-activated protein kinase signaling pathways

Biol Pharm Bull. 2008 Dec;31(12):2228-33. doi: 10.1248/bpb.31.2228.

Abstract

Semi-vioxanthin isolated from marine-derived fungus was assessed for immunoregulatory activity in mouse RAW264.7 macrophages. In the present study, the facilitative effects of semi-vioxanthin on tumor necrosis factor-alpha (TNF-alpha) and its mRNA expression and on expression of the co-stimulatory molecules, cluster of differentiation (CD) 80, CD86 and major histocompatibility complex class II (MHC II), as well as the molecular mechanism underlying the immunologic enhancement properties of semi-vioxanthin were studied. Our results clearly indicated that semi-vioxanthin treatment resulted in the degradation of IkappaB alpha, which led to the activation and nuclear translocation of the p65 subunit of nuclear factor-kappaB (NF-kappaB), as determined by immunoblotting, immunofluorescence and electrophoretic mobility shift assays (EMSA). Moreover, TNF-alpha production was prevented by NF-kappaB and mitogen-activated protein kinase (MAPK) inhibitors. Inhibition of NF-kappaB and extracellular signal regulated kinases (ERK1/2) activity by specific inhibitors blunted the effect of semi-vioxanthin on the up-regulation of CD80, CD86 and MHCII expression, but neither p38 MAPK nor c-Jun N-terminal kinase (JNK) inhibitor had this effect. Thus, we demonstrate that semi-vioxanthin regulates TNF-alpha production through NF-kappaB and MAPK signaling pathways. Activation of NF-kappaB and ERK1/2 were necessary for CD80, CD86 and MHCII expression induced by semi-vioxanthin. These data suggest that semi-vioxanthin has immunoregulatory effects.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • B7-1 Antigen / biosynthesis
  • B7-1 Antigen / genetics*
  • B7-2 Antigen / biosynthesis
  • B7-2 Antigen / genetics*
  • Blotting, Western
  • Cell Line
  • Electrophoretic Mobility Shift Assay
  • Flow Cytometry
  • Fluorescent Antibody Technique
  • Gene Expression / drug effects
  • Genes, MHC Class II / genetics*
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Macrophages / physiology*
  • Mice
  • Mitogen-Activated Protein Kinases / genetics
  • Mitogen-Activated Protein Kinases / physiology*
  • NF-kappa B / genetics
  • NF-kappa B / physiology*
  • Naphthols / isolation & purification
  • Naphthols / pharmacology*
  • Pyrones / isolation & purification
  • Pyrones / pharmacology*
  • RNA / biosynthesis
  • RNA / genetics
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction / physiology*
  • Tumor Necrosis Factor-alpha / biosynthesis
  • Tumor Necrosis Factor-alpha / genetics*
  • Up-Regulation / drug effects

Substances

  • B7-1 Antigen
  • B7-2 Antigen
  • NF-kappa B
  • Naphthols
  • Pyrones
  • Tumor Necrosis Factor-alpha
  • RNA
  • semivioxanthin
  • Mitogen-Activated Protein Kinases