Evidence supporting a key role of Lp-PLA2-generated lysophosphatidylcholine in human atherosclerotic plaque inflammation

Arterioscler Thromb Vasc Biol. 2012 Jun;32(6):1505-12. doi: 10.1161/ATVBAHA.112.249854. Epub 2012 Apr 12.

Abstract

Objective: To determine whether the level of lysophosphatidylcholine (lysoPC) generated by lipoprotein-associated phospholipase A2 (Lp-PLA2) is associated with severity of inflammation in human atherosclerotic plaques. Elevated plasma Lp-PLA2 is associated with increased cardiovascular risk. Lp-PLA2 inhibition reduces atherosclerosis. Lp-PLA2 hydrolyzes low-density lipoprotein-oxidized phospholipids generating lysoPCs. According to in vitro studies, lysoPCs are proinflammatory but the association between their generation and plaque inflammation remains unknown.

Methods and results: Inflammatory activity in carotid plaques (162 patients) was determined immunohistochemically and by analyzing cytokines in homogenates (multiplex immunoassay). LysoPCs were quantified using mass spectrometry and Lp-PLA2 and the lysoPC metabolite lysophosphatidic acid (LPA) by ELISA. There was a strong correlation among lysoPC 16:0, 18:0, 18:1, LPA, and Lp-PLA2 in plaques. LysoPC 16:0, 18:0, 18:1, LPA, and Lp-PLA2 correlated with interleukin-1β, interleukin-6, monocyte chemoattractant protein-1, macrophage inflammatory protein-1β, regulated on activation normal T-cell expressed and secreted, and tumor necrosis factor-α in plaques. High lysoPC and Lp-PLA2 correlated with increased plaque macrophages and lipids and with low content of smooth muscle cells, whereas LPA only correlated with plaque macrophages. Lp-PLA2, lysoPC 16:0, 18:0, and 18:1, but not LPA were higher in symptomatic than in asymptomatic plaques.

Conclusions: The associations among Lp-PLA2, lysoPCs, LPA, and proinflammatory cytokines in human plaques suggest that lysoPCs play a key role in plaque inflammation and vulnerability. Our findings support Lp-PLA2 inhibition as a possible strategy for the prevention of cardiovascular disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Alkyl-2-acetylglycerophosphocholine Esterase / analysis*
  • Aged
  • Biomarkers / analysis
  • Biopsy
  • Carotid Stenosis / blood
  • Carotid Stenosis / enzymology*
  • Carotid Stenosis / immunology
  • Carotid Stenosis / pathology
  • Cytokines / analysis*
  • Cytokines / blood
  • Enzyme-Linked Immunosorbent Assay
  • Female
  • Humans
  • Immunohistochemistry
  • Inflammation / blood
  • Inflammation / enzymology*
  • Inflammation / immunology
  • Inflammation / pathology
  • Inflammation Mediators / analysis*
  • Inflammation Mediators / blood
  • Lysophosphatidylcholines / analysis*
  • Lysophosphatidylcholines / blood
  • Lysophospholipids / analysis
  • Macrophages / enzymology
  • Macrophages / immunology
  • Male
  • Mass Spectrometry
  • Middle Aged
  • Muscle, Smooth, Vascular / enzymology
  • Muscle, Smooth, Vascular / immunology
  • Phospholipases A2 / analysis*
  • Plaque, Atherosclerotic / blood
  • Plaque, Atherosclerotic / enzymology*
  • Plaque, Atherosclerotic / immunology
  • Plaque, Atherosclerotic / pathology
  • Severity of Illness Index
  • T-Lymphocytes / enzymology
  • T-Lymphocytes / immunology

Substances

  • Biomarkers
  • Cytokines
  • Inflammation Mediators
  • Lysophosphatidylcholines
  • Lysophospholipids
  • Phospholipases A2
  • 1-Alkyl-2-acetylglycerophosphocholine Esterase
  • PLA2G7 protein, human
  • lysophosphatidic acid