Upregulation of pentraxin-3 in human endothelial cells after lysophosphatidic acid exposure

Arterioscler Thromb Vasc Biol. 2008 Mar;28(3):491-7. doi: 10.1161/ATVBAHA.107.158642. Epub 2007 Dec 27.

Abstract

Objective: The earliest event in atherogenesis appears to be endothelium dysfunction. Lysophosphatidic acid (LPA), one of the major bioactive lipid components of oxidized low-density lipoproteins (oxLDL), can cause the activation of endothelial cells (ECs), which start to secrete multiple proinflammatory polypeptides/proteins. The purpose of this study was to better document the proatherogenic properties of LPA using a subproteomic approach focused on the secretome of LPA-treated ECs.

Methods and results: The secretome of LPA-treated ECs was analyzed using the 2D-DIGE approach. Among the 20 spots displaying significant variations of abundance compared with the control cells, we identified pentraxin-3 by mass spectrometry. Pentraxin-3 upregulation was confirmed at the mRNA and protein level, both on immortalized and primary ECs. LPA- but also oxLDL-induced pentraxin-3 upregulation was reduced in the presence of an antagonist of the LPA-receptors and largely dependent on NFkappaB activation. Finally, we demonstrated, for the first time, the chemotactic activity of pentraxin-3 on human THP-1 monocytes by using a chemotaxis assay.

Conclusions: Our findings favor the proatherogenic role of LPA, a bioactive lipid produced by activated platelets and present in oxLDL, because it enhances pentraxin-3 secretion that could contribute to the accumulation of monocytes in the atherosclerotic lesion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analysis of Variance
  • Atherosclerosis / physiopathology
  • C-Reactive Protein / genetics
  • C-Reactive Protein / metabolism*
  • Cells, Cultured
  • Endothelial Cells / cytology
  • Endothelial Cells / drug effects*
  • Gene Expression Regulation
  • Humans
  • Immunoblotting
  • Lysophospholipids / pharmacology*
  • Probability
  • RNA, Messenger / analysis
  • Receptors, Lysophosphatidic Acid / genetics
  • Receptors, Lysophosphatidic Acid / metabolism*
  • Sensitivity and Specificity
  • Serum Amyloid P-Component / genetics
  • Serum Amyloid P-Component / metabolism*
  • Umbilical Veins / cytology
  • Up-Regulation

Substances

  • Lysophospholipids
  • RNA, Messenger
  • Receptors, Lysophosphatidic Acid
  • Serum Amyloid P-Component
  • PTX3 protein
  • C-Reactive Protein
  • lysophosphatidic acid