Cells meeting our immunophenotypic criteria of endothelial cells are large platelets
Open Access
- 24 January 2007
- journal article
- research article
- Published by Wiley in Cytometry Part B: Clinical Cytometry
- Vol. 72B (2) , 86-93
- https://doi.org/10.1002/cyto.b.20156
Abstract
Background Circulating endothelial cells (CEC) are shed from damaged vasculature, making them a rational choice to serve as surrogate marker for vascular damage. Currently, various techniques and CEC definitions are in use, and their standardization and validation is needed. A flow cytometric single platform assay defining CEC as forward light scatter (FSC)low‐to‐intermedate, sideward light scatter (SSC)low, CD45−, CD31++ and CD146+ is a promising approach to enumerate CEC because of its simplicity (Mancuso et al., Blood 2001;97:3658–3661). Here, we set out to confirm the endothelial nature of these cells. Methods We isolated cells with a FSClow‐to‐intermediate, SSClow, CD31++, CD45dim immunophenotype (termed “cells meeting our immunophenotypic criteria for endothelial cells” [CMOIC]) from healthy donors to study the expression of endothelium‐associated markers using several techniques. Special attention was paid to reagents identifying the endothelial cell‐specific marker CD146. We compared antigen expression patterns of CMOIC with those of the HUVEC endothelial cell line and lymphocytes. Electron microscopy was used to detect the presence of endothelial cell‐specific Weibel–Palade bodies in the sorted cells. Results CD146 expression was negative on CMOIC for all tested CD146 mAbs, but positive on HUVEC cells and a minor subset of T lymphocytes. Using flow cytometry, we found no expression of any endothelium‐associated marker except for CD31 and CD34. HUVEC cells were positive for all endothelial markers except for CD34. Evaluation of CMOIC morphology showed a homogenous population of cells with a highly irregular nucleus‐like structure and positive endothelial immunohistochemistry. CMOIC contained neither nuclei nor DNA. Electron microscopy revealed the absence of a nucleus, the absence of endothelial specific Weibel–Palade bodies, and revealed CMOIC to be large platelets. Conclusion The vast majority of cells with the immunophenotype FSClow‐to‐intermediate, SSClow, CD45−, CD31++ do not express CD146 and are large platelets rather than endothelial cells. © 2007 Clinical Cytometry Society.Keywords
This publication has 31 references indexed in Scilit:
- Global Gene Expression Profiling of Circulating Endothelial Cells in Patients with Metastatic CarcinomasCancer Research, 2006
- Influence of angiogenesis inhibitors on endothelial cell morphology in vitroAPMIS, 2006
- Detection of circulating endothelial cells and endothelial progenitor cells by flow cytometryCytometry Part B: Clinical Cytometry, 2005
- Circulating endothelial cellsThrombosis and Haemostasis, 2005
- Presence of endothelial progenitor cells, distinct from mature endothelial cells, within human CD146+ blood cellsThrombosis and Haemostasis, 2005
- Tumor skewing of CD34+ progenitor cell differentiation into endothelial cellsInternational Journal of Cancer, 2004
- Strategies to Investigate Circulating Endothelial Cells in CancerPathophysiology of Haemostasis and Thrombosis, 2003
- Circulating endothelial cells in pulmonary hypertensionThrombosis and Haemostasis, 2003
- S‐Endo 1, a pan‐endothelial monoclonal antibody recognizing a novel human endothelial antigenTissue Antigens, 1996
- Identification of the S-Endo 1 Endothelial-Associated AntigenBiochemical and Biophysical Research Communications, 1996