α- and β-d-Glucans from the edible mushroom Pleurotus albidus differentially regulate lipid-induced inflammation and foam cell formation in human macrophage-like THP-1 cells

Int J Biol Macromol. 2018 May:111:1222-1228. doi: 10.1016/j.ijbiomac.2018.01.131. Epub 2018 Feb 19.

Abstract

Macrophages play an essential role in lipid metabolism; however, the excessive uptake of modified lipids and cholesterol crystals (CC) leads to the formation of pro-inflammatory lipid-laden macrophages called foam cells. Since the α-1,6- and β-1,3-d-glucans from the basidiome and the mycelium of the edible mushroom Pleurotus albidus have previously been shown to regulate macrophage function, these glucans were tested in macrophage-like THP-1 cells previously exposed to acetylated low-density lipoproteins (acLDL) or CC. The glucans inhibited lipid-induced inflammation, but only the β-1,3-d-glucan regulated both the NLRP3 inflammasome activation and the expression of genes involved on lipid efflux in acLDL- or CC-pretreated cells, thereby reducing foam cell formation. In contrast, the two α-1,6-glucans tested inhibited foam cell formation only in acLDL-pretreated cells and had no effect on the expression of the peroxisome proliferator-activated receptor gamma and liver X receptor alpha genes, suggesting that these glucans regulate lipid influx rather than lipid efflux. Thus, α- and β-d-glucans differentially regulate lipid-induced inflammation and foam cell formation in macrophage-like cells. Furthermore, results emphasize that P. albidus has potential to be used as a functional food or as a source for the extraction of biologically-active glucans.

Keywords: Cholesterol crystals; NLRP3 inflammasome; Polysaccharide.

MeSH terms

  • Cell Line
  • Cholesterol / genetics
  • Foam Cells / chemistry
  • Foam Cells / drug effects*
  • Gene Expression / drug effects
  • Glucans / chemistry
  • Glucans / isolation & purification
  • Glucans / pharmacology*
  • Humans
  • Inflammation / drug therapy*
  • Inflammation / genetics
  • Inflammation / pathology
  • Lipid Metabolism / drug effects
  • Lipids / chemistry
  • Lipoproteins, LDL / genetics
  • Liver X Receptors / genetics
  • Macrophages / drug effects*
  • Macrophages / metabolism
  • Mycelium / chemistry
  • Mycelium / drug effects
  • PPAR gamma / genetics
  • Pleurotus / chemistry

Substances

  • Glucans
  • Lipids
  • Lipoproteins, LDL
  • Liver X Receptors
  • PPAR gamma
  • acetyl-LDL
  • Cholesterol