| Literature DB >> 31152059 |
Matthew J Kolar1, Srihari Konduri2, Tina Chang1, Huijing Wang2, Clare McNerlin2, Lena Ohlsson3, Magnus Härröd4, Dionicio Siegel5, Alan Saghatelian6.
Abstract
Fatty acid esters of hydroxy fatty acids (FAHFAs) are a recently discovered class of biologically active lipids. Here we identify the linoleic acid ester of 13-hydroxy linoleic acid (13-LAHLA) as an anti-inflammatory lipid. An oat oil fraction and FAHFA-enriched extract from this fraction showed anti-inflammatory activity in a lipopolysaccharide-induced cytokine secretion assay. Structural studies identified three LAHLA isomers (15-, 13-, and 9-LAHLA) as being the most abundant FAHFAs in the oat oil fraction. Of these LAHLAs, 13-LAHLA is the most abundant LAHLA isomer in human serum after ingestion of liposomes made of fractionated oat oil, and it is also the most abundant endogenous LAHLA in mouse and human adipose tissue. As a result, we chemically synthesized 13-LAHLA for biological assays. 13-LAHLA suppresses lipopolysaccharide-stimulated secretion of cytokines and expression of pro-inflammatory genes. These studies identify LAHLAs as an evolutionarily conserved lipid with anti-inflammatory activity in mammalian cells.Entities:
Keywords: FAHFAs; LAHLAs; inflammation; lipid; lipid signaling; lipid structure; lipid synthesis
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Year: 2019 PMID: 31152059 PMCID: PMC6615670 DOI: 10.1074/jbc.RA118.006956
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157