mRNA levels of CD31, CD144, CD146 and von Willebrand factor do not serve as surrogate markers for circulating endothelial cells

Circulating endothelial cells (CEC) are considered a promising marker to determine the extent of vascular damage. However, currently available and validated CEC enumeration assays are laborious, time consuming and costly, which limits their clinical utility. Here, we evaluated the feasibility of qua...

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Published inThrombosis and haemostasis Vol. 104; no. 2; p. 318
Main Authors Strijbos, Michiel H, van Krimpen, Brigitte A, Debets, Reno, Kraan, Jaco, Sleijfer, Stefan, Gratama, Jan Willem, Lamers, Cor H J
Format Journal Article
LanguageEnglish
Published Germany 01.08.2010
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Abstract Circulating endothelial cells (CEC) are considered a promising marker to determine the extent of vascular damage. However, currently available and validated CEC enumeration assays are laborious, time consuming and costly, which limits their clinical utility. Here, we evaluated the feasibility of quantifying mRNA levels of the endothelium-associated markers CD31, CD144, CD146 and von Willebrand factor (vWf) in peripheral blood (PB) of healthy donors, patients, and human umbilical veins by real-time reverse transcriptase polymerase chain reaction (RT-PCR) and their use as surrogate markers for CEC. Whole blood samples and CD146+ cell-enriched fractions were assessed for mRNA and protein expression of CD31, CD144, CD146 and vWf by RT-PCR and flow cytometry, respectively. We showed the feasibility to detect endothelial mRNA isolated from HUVEC numbers as low as 10. However, no endothelial mRNA could be measure in whole blood samples, and only low levels of CD31 and CD146 mRNA were detected in suspensions of isolated CEC with numbers up to 4,450 CEC per sample. We conclude that mRNA levels of CD31, CD144, CD146 and vWf in whole blood as detected by real time RT-PCR cannot be used as biomarkers for end-stage endothelial cells such as CEC.
AbstractList Circulating endothelial cells (CEC) are considered a promising marker to determine the extent of vascular damage. However, currently available and validated CEC enumeration assays are laborious, time consuming and costly, which limits their clinical utility. Here, we evaluated the feasibility of quantifying mRNA levels of the endothelium-associated markers CD31, CD144, CD146 and von Willebrand factor (vWf) in peripheral blood (PB) of healthy donors, patients, and human umbilical veins by real-time reverse transcriptase polymerase chain reaction (RT-PCR) and their use as surrogate markers for CEC. Whole blood samples and CD146+ cell-enriched fractions were assessed for mRNA and protein expression of CD31, CD144, CD146 and vWf by RT-PCR and flow cytometry, respectively. We showed the feasibility to detect endothelial mRNA isolated from HUVEC numbers as low as 10. However, no endothelial mRNA could be measure in whole blood samples, and only low levels of CD31 and CD146 mRNA were detected in suspensions of isolated CEC with numbers up to 4,450 CEC per sample. We conclude that mRNA levels of CD31, CD144, CD146 and vWf in whole blood as detected by real time RT-PCR cannot be used as biomarkers for end-stage endothelial cells such as CEC.
Author Debets, Reno
Kraan, Jaco
Sleijfer, Stefan
Strijbos, Michiel H
Lamers, Cor H J
van Krimpen, Brigitte A
Gratama, Jan Willem
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Snippet Circulating endothelial cells (CEC) are considered a promising marker to determine the extent of vascular damage. However, currently available and validated...
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StartPage 318
SubjectTerms Adult
Antigens, CD - genetics
Apoptosis
Biomarkers - blood
Cadherins - genetics
CD146 Antigen - genetics
Cells, Cultured
Endothelial Cells - metabolism
Endothelial Cells - pathology
Feasibility Studies
Female
Flow Cytometry
Humans
Immunomagnetic Separation
Male
Middle Aged
Platelet Endothelial Cell Adhesion Molecule-1 - genetics
Reproducibility of Results
Reverse Transcriptase Polymerase Chain Reaction
RNA, Messenger - blood
T-Lymphocytes - metabolism
von Willebrand Factor - genetics
Title mRNA levels of CD31, CD144, CD146 and von Willebrand factor do not serve as surrogate markers for circulating endothelial cells
URI https://www.ncbi.nlm.nih.gov/pubmed/20589320
Volume 104
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