The natural product phyllanthusmin C enhances IFN-γ production by human NK cells through upregulation of TLR-mediated NF-κB signaling

J Immunol. 2014 Sep 15;193(6):2994-3002. doi: 10.4049/jimmunol.1302600. Epub 2014 Aug 13.

Abstract

Natural products are a major source for cancer drug development. NK cells are a critical component of innate immunity with the capacity to destroy cancer cells, cancer-initiating cells, and clear viral infections. However, few reports describe a natural product that stimulates NK cell IFN-γ production and unravel a mechanism of action. In this study, through screening, we found that a natural product, phyllanthusmin C (PL-C), alone enhanced IFN-γ production by human NK cells. PL-C also synergized with IL-12, even at the low cytokine concentration of 0.1 ng/ml, and stimulated IFN-γ production in both human CD56(bright) and CD56(dim) NK cell subsets. Mechanistically, TLR1 and/or TLR6 mediated PL-C's activation of the NF-κB p65 subunit that in turn bound to the proximal promoter of IFNG and subsequently resulted in increased IFN-γ production in NK cells. However, IL-12 and IL-15Rs and their related STAT signaling pathways were not responsible for the enhanced IFN-γ secretion by PL-C. PL-C induced little or no T cell IFN-γ production or NK cell cytotoxicity. Collectively, we identify a natural product with the capacity to selectively enhance human NK cell IFN-γ production. Given the role of IFN-γ in immune surveillance, additional studies to understand the role of this natural product in prevention of cancer or infection in select populations are warranted.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Benzodioxoles / pharmacology*
  • CD56 Antigen / biosynthesis
  • CD56 Antigen / genetics
  • Cells, Cultured
  • Glycosides / pharmacology*
  • HEK293 Cells
  • Humans
  • Interferon-gamma / biosynthesis*
  • Interleukin-12 / pharmacology
  • Interleukin-15 / pharmacology
  • Killer Cells, Natural / immunology*
  • Lymphocyte Activation / immunology
  • RNA Interference
  • RNA, Small Interfering
  • Receptors, Interleukin-15
  • Signal Transduction / immunology
  • Toll-Like Receptor 1 / genetics
  • Toll-Like Receptor 1 / immunology
  • Toll-Like Receptor 6 / immunology
  • Transcription Factor RelA / biosynthesis
  • Transcription Factor RelA / immunology*
  • Up-Regulation

Substances

  • Benzodioxoles
  • CD56 Antigen
  • Glycosides
  • IL15 protein, human
  • Interleukin-15
  • NCAM1 protein, human
  • RNA, Small Interfering
  • Receptors, Interleukin-15
  • TLR6 protein, human
  • Toll-Like Receptor 1
  • Toll-Like Receptor 6
  • Transcription Factor RelA
  • phyllanthusmin C
  • Interleukin-12
  • Interferon-gamma