Structural Similarity with Cholesterol Reveals Crucial Insights into Mechanisms Sustaining the Immunomodulatory Activity of the Mycotoxin Alternariol

Cells. 2020 Mar 31;9(4):847. doi: 10.3390/cells9040847.

Abstract

The proliferation of molds in domestic environments can lead to uncontrolled continuous exposure to mycotoxins. Even if not immediately symptomatic, this may result in chronic effects, such as, for instance, immunosuppression or allergenic promotion. Alternariol (AOH) is one of the most abundant mycotoxins produced by Alternariaalternata fungi, proliferating among others in fridges, as well as in humid walls. AOH was previously reported to have immunomodulatory potential. However, molecular mechanisms sustaining this effect remained elusive. In differentiated THP-1 macrophages, AOH hardly altered the secretion of pro-inflammatory mediators when co-incubated with lipopolysaccharide (LPS), opening up the possibility that the immunosuppressive potential of the toxin could be related to an alteration of a downstream pro-inflammatory signaling cascade. Intriguingly, the mycotoxin affected the membrane fluidity in macrophages and it synergistically reacted with the cholesterol binding agent MβCD. In silico modelling revealed the potential of the mycotoxin to intercalate in cholesterol-rich membrane domains, like caveolae, and immunofluorescence showed the modified interplay of caveolin-1 with Toll-like Receptor (TLR) 4. In conclusion, we identified the structural similarity with cholesterol as one of the key determinants of the immunomodulatory potential of AOH.

Keywords: alternariol; cholesterol; immunomodulation; membrane.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Caveolin 1 / metabolism
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Cholesterol / chemistry*
  • Fatty Acids, Unsaturated / metabolism
  • Humans
  • Immunomodulation* / drug effects
  • Lactones / chemistry*
  • Lactones / pharmacology
  • Lipopolysaccharides / pharmacology
  • Macrophages / drug effects
  • Macrophages / metabolism
  • Membrane Fluidity / drug effects
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mycotoxins / chemistry*
  • Oxylipins / metabolism
  • Superoxides / metabolism
  • THP-1 Cells
  • Toll-Like Receptor 4 / metabolism
  • beta-Cyclodextrins / pharmacology

Substances

  • Caveolin 1
  • Fatty Acids, Unsaturated
  • Lactones
  • Lipopolysaccharides
  • Mycotoxins
  • Oxylipins
  • Toll-Like Receptor 4
  • beta-Cyclodextrins
  • Superoxides
  • Cholesterol
  • betadex
  • alternariol