A novel polysaccharide in insects activates the innate immune system in mouse macrophage RAW264 cells

PLoS One. 2014 Dec 9;9(12):e114823. doi: 10.1371/journal.pone.0114823. eCollection 2014.

Abstract

A novel water-soluble polysaccharide was identified in the pupae of the melon fly (Bactrocera cucurbitae) as a molecule that activates the mammalian innate immune response. We attempted to purify this innate immune activator using nitric oxide (NO) production in mouse RAW264 macrophages as an indicator of immunostimulatory activity. A novel acidic polysaccharide was identified, which we named "dipterose", with a molecular weight of 1.01 × 10(6) and comprising nine monosaccharides. Dipterose was synthesized in the melon fly itself at the pupal stage. The NO-producing activity of dipterose was approximately equal to that of lipopolysaccharide, a potent immunostimulator. Inhibition of Toll-like receptor 4 (TLR4) led to the suppression of NO production by dipterose. Furthermore, dipterose induced the expression of proinflammatory cytokines and interferon β (IFNβ) and promoted the activation of nuclear factor kappa B (NF-κB) in macrophages, indicating that it stimulates the induction of various cytokines in RAW264 cells via the TLR4 signaling pathway. Our results thus suggest that dipterose activates the innate immune response against various pathogenic microorganisms and viral infections. This is the first identification of an innate immune-activating polysaccharide from an animal.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Blotting, Western
  • Cells, Cultured
  • Immune System / immunology*
  • Immunity, Innate / immunology*
  • Macrophages / immunology*
  • Macrophages / metabolism
  • Macrophages / pathology
  • Mice
  • Nitric Oxide / metabolism*
  • Polysaccharides / pharmacology*
  • Pupa / physiology*
  • RNA, Messenger / genetics
  • Real-Time Polymerase Chain Reaction
  • Reverse Transcriptase Polymerase Chain Reaction
  • Tephritidae / physiology*
  • Toll-Like Receptors / genetics
  • Toll-Like Receptors / metabolism

Substances

  • Polysaccharides
  • RNA, Messenger
  • Toll-Like Receptors
  • Nitric Oxide

Grants and funding

This work was supported by the Japan Science and Technology Agency (JST), A-step start-up venture program (#AS2113025E) from the Japan Science and Technology Agency (http://www.jst.go.jp), Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (http://kaken.nii.ac.jp/), and Bussan Biotech Co., LTD (http://bussan-bio.co.jp/). The funders had role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.