Native and myeloperoxidase-oxidized low-density lipoproteins act in synergy to induce release of resolvin-D1 from endothelial cells

Atherosclerosis. 2018 May:272:108-117. doi: 10.1016/j.atherosclerosis.2018.03.012. Epub 2018 Mar 8.

Abstract

Background and aims: Oxidation of native low-density lipoproteins (LDLs-nat) plays an important role in the development of atherosclerosis. A major player in LDL-nat oxidation is myeloperoxidase (MPO), a heme enzyme present in azurophil granules of neutrophils and monocytes. MPO produces oxidized LDLs called Mox-LDLs, which cause a pro-inflammatory response in human microvascular endothelial cells (HMEC), monocyte/macrophage activation and formation of foam cells. Resolvin D1 (RvD1) is a compound derived from the metabolism of the polyunsaturated fatty acid DHA, which promotes resolution of inflammation at the ng/ml level.

Methods: In the present study, we used liquid chromatography-mass spectrometry (LC-MS/MS) to investigate the synthesis of RvD1 and its precursors - 17(S)-hydroxy docosahexaenoic acid (17S-HDHA) and docosahexaenoic acid (DHA) - by HMEC, in the presence of several concentrations of Mox-LDLs, copper-oxidized-LDLs (Ox-LDLs), and native LDLs or in mouse plasma. The LC-MS/MS method has been validated and applied to cell supernatants and plasma to measure production of RvD1 and its precursors in several conditions.

Results: Mox-LDLs played a significant role in the synthesis of RvD1 and 17S-HDHA from DHA compared to Ox-LDLs. Moreover, Mox-LDLs and LDLs-nat acted in synergy to produce RvD1. In addition, different correlations were found between RvD1 and M1 macrophages, age of mice or Cl-Tyr/Tyr ratio.

Conclusions: These results suggest that although Mox-LDLs are known to be pro-inflammatory and deleterious in the context of atherosclerosis, they are also able to induce a pro-resolution effect by induction of RvD1 from HMEC. Finally, our data also suggest that HMEC can produce RvD1 on their own.

Keywords: Atherosclerosis; Inflammation; Lipid mediators; Lipidomics; Low-density lipoproteins (LDLs); Myeloperoxidase; Omega-3 fatty acids; Tandem mass spectrometry.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Atherosclerosis / metabolism
  • Calibration
  • Cell Line
  • Chromatography, Liquid
  • Copper
  • Docosahexaenoic Acids / biosynthesis*
  • Endothelial Cells / cytology*
  • Humans
  • Inflammation
  • Limit of Detection
  • Lipids / blood
  • Lipoproteins, LDL / blood*
  • Macrophages
  • Mass Spectrometry
  • Mice
  • Mice, Inbred C57BL
  • Oxygen
  • Peroxidase / metabolism*
  • RNA, Small Interfering / metabolism
  • Reactive Oxygen Species / metabolism

Substances

  • Lipids
  • Lipoproteins, LDL
  • RNA, Small Interfering
  • Reactive Oxygen Species
  • oxidized low density lipoprotein
  • resolvin D1
  • Docosahexaenoic Acids
  • Copper
  • Peroxidase
  • Oxygen