Apoptosis of human macrophages by Flt-4 signaling: implications for atherosclerotic plaque pathology

Cardiovasc Res. 2006 Sep 1;71(4):774-84. doi: 10.1016/j.cardiores.2006.06.012. Epub 2006 Jun 12.

Abstract

Background: Neointimal inflammation and angiogenesis are important contributors of progression and destabilization of the atherosclerotic plaque. While the role of vascular endothelial growth factor (VEGF) and its receptors VEGF-R1 (Flt-1) and VEGF-R2 (Flk-1) in this process has clearly been defined, expression of the VEGF-R3 (Flt-4) has only been documented on lymphatic and tumor endothelium. This study examined Flt-4 expression in human atherosclerotic plaque and explored its implications for atherosclerotic disease.

Methods and results: Carotid artery thrombendartherectomy specimens from 10 patients with unstable plaque were stained for Flt-4 and its specific growth factors VEGF-C and VEGF-D. Microvascular endothelial cells (MVEC) stained positive for VEGF-C and -D, but not for Flt-4. Interestingly, macrophages within inflammatory perivascular regions coexpressed Flt-4, VEGF-C and VEGF-D. In vitro studies confirmed the expression of Flt-4, VEGF-C and VEGF-D in human monocytes and cultured macrophages. Treatment of macrophages with VEGF-D induced apoptosis as determined by annexin V staining, by immunoblotting of activated caspase 3, and by the ratio of Bcl-2/Bax as well as by DNA fragmentation. Immunohistochemical studies of advanced human carotid atherosclerotic plaque confirmed the coexpression of Flt-4 with activated caspase 3 and TUNEL staining in macrophages, indicating an ongoing apoptotic process.

Conclusion: Human monocytes/macrophages express VEGF-C and -D and their receptor Flt-4 in vitro and in vivo within advanced atherosclerotic lesions. Flt-4, in turn, mediates monocyte/macrophage apoptosis and may this way alter plaque stability.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Apoptosis / drug effects
  • Blotting, Western
  • Carotid Arteries / metabolism
  • Carotid Arteries / pathology
  • Carotid Artery Diseases / metabolism*
  • Caspase 3 / metabolism
  • Cell Line
  • Cells, Cultured
  • DNA Fragmentation
  • Female
  • Humans
  • Immunohistochemistry
  • Intercellular Signaling Peptides and Proteins / analysis
  • Intercellular Signaling Peptides and Proteins / metabolism*
  • Macrophages / metabolism*
  • Macrophages / pathology
  • Male
  • Microscopy, Fluorescence
  • Middle Aged
  • Reverse Transcriptase Polymerase Chain Reaction
  • Signal Transduction / physiology*
  • Vascular Endothelial Growth Factor C / metabolism
  • Vascular Endothelial Growth Factor C / pharmacology
  • Vascular Endothelial Growth Factor D / metabolism
  • Vascular Endothelial Growth Factor D / pharmacology
  • Vascular Endothelial Growth Factor Receptor-3 / analysis
  • Vascular Endothelial Growth Factor Receptor-3 / physiology*

Substances

  • Intercellular Signaling Peptides and Proteins
  • Vascular Endothelial Growth Factor C
  • Vascular Endothelial Growth Factor D
  • Vascular Endothelial Growth Factor Receptor-3
  • Caspase 3