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Characteristics of circulating endothelial cells obtained from non-ST-segment elevation myocardial infarction patients with additional diastolic dysfunction of left ventricle observed in echocardiography


- Biology of Lipid Disorders Department, Chair of Biology and Environmental Sciences, Poznan University of Medical Sciences, Poznan, Poland
- Department of Cardiology, J. Strus Hospital, Szwajcarska 3, 61-285 Poznan, Poland
- Department of Cardiology, Hospital of Nowa Sol, Poland
- Institute for Medical Immunology, Berlin-Brandenburg Center für Regenerative Therapies, Core Unit Biomarker, Charité University Medicine, Berlin, Germany
- Zablab sp. z o.o, Poznan, Poland
- HaimaChek Inc, Santa Monica, Santa Monica, CA,, United States
- Bayer AG, Biomarker Research, Berlin, Germany
open access
Abstract
Background: Circulating endothelial cells (CEC) may be used to find new strategies for the early diagnosis of cardiovascular diseases. The major objective of the project is to broaden knowledge of CEC biology by determining their phenotypic characteristics. The additional aim is to clarify whether on the basis of these information it is possible to identify the origin of CEC release (from various cardiovascular compartments).
Methods: Circulating endothelial cells were collected from arterial blood prior to angiography, as well as from arterial and venous blood obtained after angiography/coronary angioplasty, from 18 patients with non-ST-segment elevation myocardial infarction (NSTEMI). CECs were quantified by flow cytometry and defined as Syto16 (dye)+, CD45dim/neg, CD31+ and CD146+. The additional CD36+ was establish as a marker of endothelial cells released from small vessels of the microcirculation.
Results: The total number of CECs increased significantly after the percutaneous transluminal coronary angioplasty (PTCA) in the arterial system. Number of CECs isolated at similar time points (after invasive procedure) did not differ significantly between arteries and veins, but the number of CD36+ CECs after coronary angioplasty was significantly higher in the venous system, than in the arterial system.
Conclusions: The number of CD36+ in artery samples obtained after coronary angioplasty (PTCA) had tendency to be decreased (in comparison to the sample obtained before angiography). It was major difference between those who had PTCA performed vs. those who had not.
Abstract
Background: Circulating endothelial cells (CEC) may be used to find new strategies for the early diagnosis of cardiovascular diseases. The major objective of the project is to broaden knowledge of CEC biology by determining their phenotypic characteristics. The additional aim is to clarify whether on the basis of these information it is possible to identify the origin of CEC release (from various cardiovascular compartments).
Methods: Circulating endothelial cells were collected from arterial blood prior to angiography, as well as from arterial and venous blood obtained after angiography/coronary angioplasty, from 18 patients with non-ST-segment elevation myocardial infarction (NSTEMI). CECs were quantified by flow cytometry and defined as Syto16 (dye)+, CD45dim/neg, CD31+ and CD146+. The additional CD36+ was establish as a marker of endothelial cells released from small vessels of the microcirculation.
Results: The total number of CECs increased significantly after the percutaneous transluminal coronary angioplasty (PTCA) in the arterial system. Number of CECs isolated at similar time points (after invasive procedure) did not differ significantly between arteries and veins, but the number of CD36+ CECs after coronary angioplasty was significantly higher in the venous system, than in the arterial system.
Conclusions: The number of CD36+ in artery samples obtained after coronary angioplasty (PTCA) had tendency to be decreased (in comparison to the sample obtained before angiography). It was major difference between those who had PTCA performed vs. those who had not.
Keywords
circulating endothelial cells, NSTEMI, diastolic dysfunction


Title
Characteristics of circulating endothelial cells obtained from non-ST-segment elevation myocardial infarction patients with additional diastolic dysfunction of left ventricle observed in echocardiography
Journal
Issue
Pages
295-302
Published online
2018-09-13
Page views
1356
Article views/downloads
624
DOI
10.5603/CJ.a2018.0110
Pubmed
Bibliographic record
Cardiol J 2020;27(3):295-302.
Keywords
circulating endothelial cells
NSTEMI
diastolic dysfunction
Authors
Pawel Burchardt
Maura Farinacci
Magdalena Mayer
Klaus Luecke
Thomas Krahn
Jaroslaw Manczak
Marek Slomczynski
Jaroslaw Hiczkiewicz
Janusz Rzezniczak


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