An Optimized Flow Cytometry Protocol for Analysis of Angiogenic Monocytes and Endothelial Progenitor Cells in Peripheral Blood

被引:36
|
作者
Hristov, Mihail [1 ]
Schmitz, Susanne [1 ]
Schuhmann, Christoph [2 ]
Leyendecker, Thorsten [3 ]
von Hundelshausen, Philipp [1 ,3 ]
Kroetz, Florian [2 ]
Sohn, Hae-Young [2 ]
Nauwelaers, Frans A. [4 ]
Weber, Christian [1 ]
机构
[1] Rhein Westfal TH Aachen, IMCAR, D-52074 Aachen, Germany
[2] Univ Munich, Dept Cardiol, Munich, Germany
[3] Rhein Westfal TH Aachen, Dept Cardiol Pulmol & Vasc Med, D-52074 Aachen, Germany
[4] BD Biosci Europe, Erembodegem, Belgium
关键词
atherosclerosis; bone marrow; remodeling; angiogenesis; leukocytes; CORONARY-ARTERY-DISEASE; TIE2-EXPRESSING MONOCYTES; VASCULAR REPAIR; NUMBER; EXPRESSION;
D O I
10.1002/cyto.a.20772
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Circulating adult CD34(+)VEGFR2(+) endothelial progenitor cells (EPCs) have been shown to differentiate into endothelial cells, thus contributing to vascular homeostasis. Furthermore, a subset of circulating CD14(+) monocytes coexpresses CD16 together with the angiopoietin receptor Tie2 and has been functionally implicated in tumor angiogenesis. However, clinically applicable protocols for flow cytometric quantification of EPCs and Tie2(+) monocytes in peripheral blood and a consensus on reference values remain elusive. The number of Tie2(+)CD14(+)CD16(mid) angiogenic monocytes and CD34(+)VEGFR2(+)CD45(low/-) EPCs was assessed in the peripheral venous blood of patients with stable coronary artery disease by three-color flow cytometry using specific monoclonal antibodies conjugated to PerCP, PE, PE-Cy7, APC, and APC-Cy7. Scatter multigating with exclusion of dead cells was performed to dissect complex mononuclear cell populations. This analysis was further refined by matching bright fluorochromes (PE-Cy7, PE, APC) with dimly expressed markers (CD34, VEGFR2, Tie2), by automatic compensation for minimizing fluorescence spillover and by using fluorescence-minus-one (FMO) controls to determine positive/negative boundaries. Presuming a Gaussian distribution, we obtained average values (mean +/- SD) of 1.45 +/- 1.29% for Tie2(+)CD14(+)CD16(mid) monocytes (n = 11, range: 0.12-3.64%) and 0.019 +/- 0.013% for CD34(+)VEGFR2(+)CD45(low/-) EPCs (n = 17, range: 0.003-0.042%). The intra- and inter-assay variability was 1.6% and 4.5%, respectively. We have optimized a fast and sensitive assay for the flow cytometric quantification of circulating angiogenic monocytes and EPCs in cardiovascular medicine. This protocol may represent a basis for standardized analysis and monitoring of these cell subsets to define their normal range and prognostic/diagnostic value in clinical use. (C) 2009 International Society for Advancement of Cytometry
引用
收藏
页码:848 / 853
页数:6
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