High density lipoprotein efficiently accepts surface but not internal oxidised lipids from oxidised low density lipoprotein

• Published in: Biochimica et biophysica acta 2016-02, Vol.1861 (2), p.69-77
• Main Authors: Rasmiena, Aliki A., Barlow, Christopher K., Ng, Theodore W., Tull, Dedreia, Meikle, Peter J.
• Format: Article
• Language: English
• Subjects: Adult; Aged; Anti-oxidative; Biological Transport; Cholesterol Esters - chemistry; Cholesteryl ester; Copper - chemistry; Fasting; Female; Humans; Hydroxycholesterols - chemistry; Ketocholesterols - chemistry; Lipidomic; Lipoproteins, HDL - chemistry; Lipoproteins, HDL - isolation & purification; Lipoproteins, LDL - chemistry; Lipoproteins, LDL - isolation & purification; Lysophosphatidylcholines - chemistry; Male; Middle Aged; Oxidants - chemistry; Oxidation-Reduction; Oxysterols; Phosphatidylcholine; Phosphatidylcholines - chemistry; Phosphatidylserines - chemistry; Sphingomyelins - chemistry; Transfer; Triglycerides - chemistry; Triglycerides - isolation & purification
• ISSN: 1388-1981; 0006-3002; 1879-2618
• DOI: 10.1016/j.bbalip.2015.11.002

Oxidised low density lipoprotein (oxLDL) contributes to atherosclerosis, whereas high density lipoprotein (HDL) is known to be atheroprotective due, at least in part, to its ability to remove oxidised lipids from oxLDL. The molecular details of the lipid transfer process are not fully understood. We aimed to identify major oxidised lipid species of oxLDL and investigate their transfer upon co-incubation with HDL with varying levels of oxidation. A total of 14 major species of oxidised phosphatidylcholine and oxidised cholesteryl ester from oxLDL were identified using an untargeted mass spectrometry approach. HDL obtained from pooled plasma of normolipidemic subjects (N=5) was oxidised under mild and heavy oxidative conditions. Non-oxidised (native) HDL and oxidised HDL were co-incubated with oxLDL, re-isolated and lipidomic analysis was performed. Lipoprotein surface lipids, oxidised phosphatidylcholines and oxidised cholesterols (7-ketocholesterol and 7β-hydroxycholesterol), but not internal oxidised cholesteryl esters, were effectively transferred to native HDL. Saturated and monounsaturated lyso-phosphatidylcholines were also transferred from the oxLDL to native HDL. These processes were attenuated when HDL was oxidised under mild and heavy oxidative conditions. The impaired capacities were accompanied by an increase in a ratio of sphingomyelin to phosphatidylcholine and a reduction in phosphatidylserine content in oxidised HDL, both of which are potentially important regulators of the oxidised lipid transfer capacity of HDL. Our study has revealed the differential transfer efficiency of surface and internal oxidised lipids from oxLDL and their acceptance onto HDL. These capacities were modulated when HDL was itself oxidised. •OxPC and oxCE species were identified in oxLDL.•HDL efficiently accepts oxPC but not oxCE from oxLDL.•HDL accepts saturated- and monounsaturated lyso-PC from oxLDL.•The oxidised-lipid transfer capacity of HDL was attenuated by oxidation.•The impaired lipid transfer capacity of HDL was accompanied by altered lipid composition.