Lipidomics Revealed the Suppression of 5-PAHSA from Human Milk on Macrophage Foam Cell Formation

Human milk contains bioactive lipids that provide long-term cardiovascular benefits, but the specific components and mechanisms remain unclear. This study aimed to identify lactation stage-specific lipid changes and assess the role of 5-palmitic acid ester of hydroxystearic acid (5-PAHSA) in macrophage foam cell formation. Nontargeted lipidomics across colostrum, transitional, and mature milk identified 189 significantly modulated lipids, with 5-PAHSA being 1.74-fold higher in colostrum than in mature milk (p < 0.0001). In an oxidized low-density lipoprotein-induced foam cell model, 5-PAHSA reduced intracellular lipid accumulation, decreased the Cholesterol ester/total Cholesterol ratio by 25% (p < 0.01), upregulated Cholesterol efflux/hydrolysis genes (ABCA1, ABCG1, nCEH), and downregulated uptake/esterification genes (CD36, SRA, ACAT1). Moreover, 5-PAHSA enhanced autophagic flux, possibly via the FOXO1/TFEB pathway, thereby suppressing macrophage foam cell formation. This study provides novel insights into lipid components and cardiovascular bioactivity of human milk throughout lactation.

FAHFAs; FoxO1; TFEB; autophagy; foam cells; human milk; lipidomics.