Dissociation of phenotypic and functional endothelial progenitor cells in patients undergoing percutaneous coronary intervention

• Published in: Heart (British Cardiac Society) Vol. 95; no. 24; p. 2003
• Main Authors: Mills, N L, Tura, O, Padfield, G J, Millar, C, Lang, N N, Stirling, D, Ludlam, C, Turner, M L, Barclay, G R, Newby, D E
• Format: Journal Article
• Language: English
• Published: England 01-12-2009
• Subjects: Angioplasty, Balloon, Coronary - adverse effects; C-Reactive Protein - metabolism; Case-Control Studies; Coronary Disease - therapy; Endothelial Cells - cytology; Endothelial Cells - physiology; Female; Heart Injuries - pathology; Humans; Leukocyte Count; Leukocytes, Mononuclear - physiology; Male; Middle Aged; Myocardial Infarction - etiology; Myocardial Infarction - pathology; Myocarditis - etiology; Myocarditis - pathology; Myocytes, Cardiac - pathology; Phenotype; Prospective Studies; Stem Cells - cytology; Stem Cells - physiology
• ISSN: 1468-201X
• DOI: 10.1136/hrt.2008.163162

Endothelial progenitor cells (EPCs) are circulating mononuclear cells with the capacity to mature into endothelial cells and contribute to vascular repair. We assessed the effect of local vascular injury during percutaneous coronary intervention (PCI) on circulating EPCs in patients with coronary artery disease.
Prospective case-control study in a university teaching hospital.
54 patients undergoing elective coronary angiography.
EPCs were quantified by flow cytometry (CD34(+)KDR(+) phenotype) complemented by real-time polymerase chain reaction (PCR), and the colony forming unit (CFU-EC) functional assay, before and during the first 24 hours after diagnostic angiography (n = 27) or PCI (n = 27).
Coronary intervention, but not diagnostic angiography, resulted in an increase in blood neutrophil count (p<0.001) and C-reactive protein concentrations (p = 0.001) in the absence of significant myocardial necrosis. Twenty-four hours after PCI, CFU-ECs increased threefold (median [IQR], 4.4 [1.3-13.8] vs 16.0 [2.1-35.0], p = 0.01), although circulating CD34(+)KDR(+) cells (0.019% (SEM 0.004%) vs 0.016% (0.003%) of leucocytes, p = 0.62) and leucocyte CD34 mRNA (relative quantity 2.3 (0.5) vs 2.1 (0.4), p = 0.21) did not. There was no correlation between CFU-ECs and CD34(+)KDR(+) cells.
Local vascular injury following PCI results in a systemic inflammatory response and increases functional CFU-ECs. This increase was not associated with an early mobilisation of CD34(+)KDR(+) cells, suggesting these cells are not the primary source of EPCs involved in the immediate response to vascular injury.