RNA and a cell wall component of Enterococcus faecalis IC-1 are required for phagocytosis and interleukin 12 production by the mouse macrophage cell line J774.1

Biosci Biotechnol Biochem. 2017 Jun;81(6):1099-1105. doi: 10.1080/09168451.2017.1295799. Epub 2017 Apr 13.

Abstract

Enterococcus faecalis is a resident lactic acid bacterium in the human intestine. Its immunostimulatory action was reported to be enhanced by heat sterilization. To investigate its beneficial actions, we evaluated the ability of 10 E. faecalis strains to induce interleukin-12 (IL-12) production in a mouse macrophage cell line, J774.1 and found that the strain, E. faecalis IC-1, had a potent IL-12-inducing ability. Furthermore, we investigated the underlying mechanism by treating IC-1 cells with RNase or lysozyme. Its activity almost disappeared and an antagonist of Toll-like receptor (TLR) 7 inhibited this activity. Moreover, lysozyme-treated IC-1 bacteria were not phagocytized by J774.1 cells, and did not induce IL-12 production. Based on our results, we propose that macrophages recognize the cell wall components of IC-1, leading to phagocytosis. The IC-1 RNA is then recognized by TLR7, which induces the production of IL-12.

Keywords: Enterococcus faecalis; RNA; cell wall component; interleukin 12.

MeSH terms

  • Animals
  • Cell Line
  • Cell Wall / chemistry
  • Cell Wall / drug effects
  • Cell Wall / immunology*
  • Coculture Techniques
  • Enterococcus faecalis / chemistry
  • Enterococcus faecalis / drug effects
  • Enterococcus faecalis / immunology*
  • Gene Expression
  • Interleukin-12 / biosynthesis
  • Interleukin-12 / immunology*
  • Macrophages / cytology
  • Macrophages / drug effects
  • Macrophages / immunology*
  • Membrane Glycoproteins / antagonists & inhibitors
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / immunology
  • Mice
  • Muramidase / chemistry
  • Muramidase / pharmacology
  • Oligonucleotides / pharmacology
  • Phagocytosis / drug effects
  • RNA, Bacterial / chemistry
  • RNA, Bacterial / immunology*
  • Ribonucleases / chemistry
  • Ribonucleases / pharmacology
  • Toll-Like Receptor 7 / antagonists & inhibitors
  • Toll-Like Receptor 7 / genetics
  • Toll-Like Receptor 7 / immunology

Substances

  • Membrane Glycoproteins
  • Oligonucleotides
  • RNA, Bacterial
  • Tlr7 protein, mouse
  • Toll-Like Receptor 7
  • Interleukin-12
  • Ribonucleases
  • Muramidase