摘要：SummaryAlthough microbe-associated molecular pattern (MAMP) molecules can promote cholesterol accumulation in macrophages, the existence of a host-derived MAMP inactivation mechanism that prevents foam cell formation has not been described. Here, we tested the ability of acyloxyacyl hydrolase (AOAH), the host lipase that inactivates gram-negative bacterial lipopolysaccharides (LPSs), to prevent foam cell formation in mice. Following exposure to small intraperitoneal dose(s) of LPSs,Aoah−/−macrophages produced more low-density lipoprotein receptor and less apolipoprotein E and accumulated more cholesterol than didAoah+/+macrophages. TheAoah−/−macrophages also maintained several pro-inflammatory features. Using a perivascular collar placement model, we found thatAoah−/−mice developed more carotid artery foam cells than didAoah+/+mice after they had been fed a high fat, high cholesterol diet, and received small doses of LPSs. This is the first demonstration that an enzyme that inactivates a stimulatory MAMPin vivocan reduce cholesterol accumulation and inflammation in arterial macrophages.Graphical abstractDisplay OmittedHighlights•Acyloxyacyl hydrolase prevents LPS-induced cholesterol accumulation in macrophages•AOAH also prevents prolonged inflammation after LPS exposure•AOAH enhances mitochondrial function in LPS-exposed macrophages•AOAH ameliorates LPS-induced foam cell accumulation in carotid arterial lesionsLipid; Molecular biology; Cell biology
