Citrus pectin attenuates endotoxin shock via suppression of Toll-like receptor signaling in Peyer's patch myeloid cells

J Nutr Biochem. 2017 Dec:50:38-45. doi: 10.1016/j.jnutbio.2017.07.016. Epub 2017 Aug 12.

Abstract

Pectin, a water-soluble dietary fiber, has been found to improve survival in endotoxin shock. However, the underlying mechanism by which pectin exerts its protective effect against endotoxin shock remains unknown. Apart from its prebiotic effects, it has been suggested that pectin directly affects immune cells to regulate inflammatory responses. In this study, we investigated the direct effect of pectin in murine model of endotoxin shock. Citrus pectin solution was administered to male C57BL/6 mice for 10 days. Thereafter, hypothermia was induced in the mice with intraperitoneal injection of lipopolysaccharide (LPS). The pectin-treated mice showed attenuation of both the decrease in rectal temperature and increase in serum IL-6 level as compared to vehicle control mice. Simultaneously, the pectin-treated mice showed reduced levels of inflammatory cytokine mRNA in Peyer's patches and mesenteric lymph nodes, but not in the spleen. Peyer's patch cells from the pectin-treated mice were sorted and their levels of IL-6 production on LPS stimulation were measured. The results of ex vivo analysis indicated that IL-6 secretion from CD11c+ cells was suppressed by oral administration of pectin. Furthermore, IL-6 secretion from Toll-like receptor (TLR)-activated RAW264.7 cells was suppressed by pretreatment with pectin in vitro. This suppression was observed even with degraded pectin pretreatment but not with polygalacturonic acid, as the principal constituent of the pectin backbone. Taken together, these results suggest that pectin intake suppresses TLR-induced inflammatory cytokine expression in Peyer's patch myeloid cells, presumably through inhibition of TLR signaling by the pectin side chains.

Keywords: Endotoxin shock; IL-6; Inflammation; Macrophage; Pectin; Peyer's patch.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Anti-Inflammatory Agents, Non-Steroidal / metabolism
  • Anti-Inflammatory Agents, Non-Steroidal / therapeutic use*
  • CD11c Antigen / metabolism
  • Cell Survival
  • Citrus / chemistry
  • Gene Expression Regulation
  • Interleukin-6 / blood
  • Interleukin-6 / metabolism
  • Lipopolysaccharides / toxicity
  • Macrophages / immunology
  • Macrophages / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Myeloid Cells / immunology
  • Myeloid Cells / metabolism
  • Pectins / metabolism
  • Pectins / therapeutic use*
  • Peyer's Patches / immunology
  • Peyer's Patches / metabolism*
  • Prebiotics*
  • RAW 264.7 Cells
  • Shock, Septic / chemically induced
  • Shock, Septic / immunology
  • Shock, Septic / metabolism
  • Shock, Septic / prevention & control*
  • Signal Transduction*
  • Toll-Like Receptors / agonists
  • Toll-Like Receptors / antagonists & inhibitors*
  • Toll-Like Receptors / metabolism

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • CD11c Antigen
  • Interleukin-6
  • Lipopolysaccharides
  • Prebiotics
  • Toll-Like Receptors
  • interleukin-6, mouse
  • lipopolysaccharide, Escherichia coli O111 B4
  • Pectins