High-reproducible flow cytometric endothelial progenitor cell determination in human peripheral blood as CD34+/CD144+/CD3-lymphocyte sub-population

被引:25
作者
Redondo, Santiago [1 ]
Hristov, Mihail [2 ,3 ]
Gordillo-Moscoso, Antonio A. [1 ]
Ruiz, Emilio [1 ]
Weber, Christian [2 ]
Tejerina, Teresa [1 ]
机构
[1] Univ Complutense, Dept Pharm, Sch Med, E-28040 Madrid, Spain
[2] RWTH Aachen Univ Hosp, Inst Mol Cardiovasc Res, Aachen, Germany
[3] RWTH Aachen Univ Hosp, Interdisciplinary Ctr Clin Res BIOMAT, Aachen, Germany
关键词
flow cytometry; endothelial progenitor cells; markers;
D O I
10.1016/j.jim.2008.02.011
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Although determination of circulating endothelial progenitor cell (EPC) in peripheral blood by flow cytometry is an emerging marker for cardiovascular medicine, a common standardized protocol is still not available, due to the low numbers achieved in peripheral blood. In the present paper we describe a novel technique for EPC quantification as CD34+/CD144+/CD3-cells within the lymphocyte gate, which increases the percentages of EPC positivity described before and also offers high intra-assay reproducibility. These improvements are based on a gating strategy for big-sized lymphocytes, smooth fixation and cytometric clearance of CD3+ lymphocytes (T-cells). This last procedure is able to increase intra-assay Pearson's correlation from 0.8517 to 0.8908. Therefore, the technical setting described here offers a high-performance and clinically oriented EPC determination strategy in human peripheral blood. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:21 / 27
页数:7
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