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
2018 (English)In: International Journal of Biological Macromolecules, ISSN 0141-8130, E-ISSN 1879-0003, Vol. 111, p. 1222-1228Article in journal (Refereed) Published
Abstract [en]
Macrophages play an essential role in lipid metabolism; however, the excessive uptake of modified lipids andcholesterol crystals (CC) leads to the formation of pro-inflammatory lipid-laden macrophages called foam cells.Since theα-1,6- andβ-1,3-D-glucans from the basidiome and the mycelium of the edible mushroomPleurotusalbidushave previously been shown to regulate macrophage function, these glucans were tested in macro-phage-like THP-1 cells previously exposed to acetylated low-density lipoproteins (acLDL) or CC. The glucansinhibited lipid-induced inflammation, but only theβ-1,3-D-glucan regulated both the NLRP3 inflammasome ac-tivation and the expression of genes involved on lipid efflux in acLDL- or CC-pretreated cells, thereby reducingfoam cell formation. In contrast, the twoα-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 gammaand liver X receptor alpha genes, suggesting that these glucans regulate lipid influx rather than lipid efflux.Thus,α-andβ-D-glucans differentially regulate lipid-induced inflammation and foam cell formation in macro-phage-like cells. Furthermore, results emphasize thatP. albidushas potential to be used as a functional food oras a source for the extraction of biologically-active glucans.
Place, publisher, year, edition, pages
Elsevier, 2018. Vol. 111, p. 1222-1228
Keywords [en]
Cholesterol crystals, NLRP3 inflammasome, Polysaccharide
National Category
Cell Biology
Identifiers
URN: urn:nbn:se:oru:diva-82819DOI: 10.1016/j.ijbiomac.2018.01.131ISI: 000429391000138PubMedID: 29366884Scopus ID: 2-s2.0-85041575208OAI: oai:DiVA.org:oru-82819DiVA, id: diva2:1437403
Note
Funding Agency:
Sao Paulo Research Foundation (FAPESP), Grant Number: 2013/07914-8
FAPESP, Grant Number: 2016/05083-0
National Council for Scientific and Technological Development CNPq, Grant Number: 310889/2014-6
2020-06-092020-06-092021-01-26Bibliographically approved