Endothelial cells release phenotypically and quantitatively distinct microparticles in activation and apoptosis

Thromb Res. 2003 Feb 15;109(4):175-80. doi: 10.1016/s0049-3848(03)00064-1.

Abstract

Background: Endothelial cells (EC) shed endothelial microparticles (EMP) in activation and apoptosis.

Objectives: We compared the antigenic expression of EMP species released during activation as compared to apoptosis, in three cell lines.

Methods: EC from renal and brain microvascular (MiVEC) and coronary macrovascular (MaVEC) origin were incubated with TNF-alpha to induce activation, or deprived of growth factors to induce apoptosis. Antigens expressed on EMP and EC were assayed flow cytometrically and included constitutive markers (CD31, CD51/61, CD105), inducible markers (CD54, CD62E and CD106), and annexin V binding.

Results: It was found that in apoptosis, constitutive markers in EMP were markedly increased (CD31>CD105), with a concomitant decrease in expression in EC. Annexin V EC surface binding and annexin V+ EMP were more sharply increased in apoptosis than in activation. In contrast, in activation, inducible markers in EMP were markedly increased in both EMP and EC (CD62E>CD54>CD106). Coronary MaVEC released significantly less EMP than MiVEC.

Conclusion: EC release qualitatively and quantitatively distinct EMP during activation compared to apoptosis. Analysis of EMP phenotypic signatures may provide clinically useful information on the status of the endothelium.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / analysis
  • Apoptosis*
  • Biomarkers / analysis
  • Brain / blood supply
  • Cell Line
  • Coronary Vessels
  • Endothelial Cells / metabolism*
  • Endothelium, Vascular / pathology*
  • Exocytosis
  • Humans
  • Immunophenotyping
  • Kidney / blood supply

Substances

  • Antigens, CD
  • Biomarkers