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Circulating Apoptotic Progenitor Cells in Patients with Congestive Heart Failure

BACKGROUND: Circulating CD34+ endothelial progenitor cells (EPCs) are capable of differentiating into mature endothelial cells to assist in angiogenesis and vasculogenesis. We sought to quantify the numbers of apoptotic progenitors in patients with congestive heart failure. METHODS AND RESULTS: Peri...

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Autores principales: Geft, Dael, Schwartzenberg, Shmuel, Rogowsky, Ori, Finkelstein, Ariel, Ablin, Jacob, Maysel-Auslender, Sofia, Wexler, Dov, Keren, Gad, George, Jacob
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2528948/
https://www.ncbi.nlm.nih.gov/pubmed/18800166
http://dx.doi.org/10.1371/journal.pone.0003238
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author Geft, Dael
Schwartzenberg, Shmuel
Rogowsky, Ori
Finkelstein, Ariel
Ablin, Jacob
Maysel-Auslender, Sofia
Wexler, Dov
Keren, Gad
George, Jacob
author_facet Geft, Dael
Schwartzenberg, Shmuel
Rogowsky, Ori
Finkelstein, Ariel
Ablin, Jacob
Maysel-Auslender, Sofia
Wexler, Dov
Keren, Gad
George, Jacob
author_sort Geft, Dael
collection PubMed
description BACKGROUND: Circulating CD34+ endothelial progenitor cells (EPCs) are capable of differentiating into mature endothelial cells to assist in angiogenesis and vasculogenesis. We sought to quantify the numbers of apoptotic progenitors in patients with congestive heart failure. METHODS AND RESULTS: Peripheral blood mononuclear cells were isolated by Ficoll density-gradient from 58 patients with various degrees of heart failure and 23 matched controls. Apoptosis in progenitor CD34+ cells was assessed using the Annexin V-PE/PI detection kit, and FACS analysis was performed with triple staining for CD34, annexin-V and propidium iodide. The percentage of early and late apoptotic progenitor cells was determined in the subject groups and was correlated with clinical characteristics. While there was no significant difference in total CD34 positive cells or early apoptotic progenitors between control subjects and CHF patients (p = 0.42) or between severe and mild/moderate CHF groups (p = 0.544), there was an elevated number of late apoptotic progenitors in the severe CHF group compared with the mild/moderate CHF group (p =  0.03). Late apoptotic progenitors were significantly increased in CHF patients as compared to matched controls. There was also an inverse correlation between late apoptotic progenitors and ejection fraction (r = −0.252, p = 0.028) as well as a positive association with NYHA class (r = 0.223, p = 0.046). CONCLUSION: Severe heart failure patients exhibited higher numbers of late apoptotic progenitors, and this was positively associated with NYHA class and negatively correlated with ejection fraction. This finding may shed light on the numerous factors governing the pathophysiology of CHF.
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spelling pubmed-25289482008-09-18 Circulating Apoptotic Progenitor Cells in Patients with Congestive Heart Failure Geft, Dael Schwartzenberg, Shmuel Rogowsky, Ori Finkelstein, Ariel Ablin, Jacob Maysel-Auslender, Sofia Wexler, Dov Keren, Gad George, Jacob PLoS One Research Article BACKGROUND: Circulating CD34+ endothelial progenitor cells (EPCs) are capable of differentiating into mature endothelial cells to assist in angiogenesis and vasculogenesis. We sought to quantify the numbers of apoptotic progenitors in patients with congestive heart failure. METHODS AND RESULTS: Peripheral blood mononuclear cells were isolated by Ficoll density-gradient from 58 patients with various degrees of heart failure and 23 matched controls. Apoptosis in progenitor CD34+ cells was assessed using the Annexin V-PE/PI detection kit, and FACS analysis was performed with triple staining for CD34, annexin-V and propidium iodide. The percentage of early and late apoptotic progenitor cells was determined in the subject groups and was correlated with clinical characteristics. While there was no significant difference in total CD34 positive cells or early apoptotic progenitors between control subjects and CHF patients (p = 0.42) or between severe and mild/moderate CHF groups (p = 0.544), there was an elevated number of late apoptotic progenitors in the severe CHF group compared with the mild/moderate CHF group (p =  0.03). Late apoptotic progenitors were significantly increased in CHF patients as compared to matched controls. There was also an inverse correlation between late apoptotic progenitors and ejection fraction (r = −0.252, p = 0.028) as well as a positive association with NYHA class (r = 0.223, p = 0.046). CONCLUSION: Severe heart failure patients exhibited higher numbers of late apoptotic progenitors, and this was positively associated with NYHA class and negatively correlated with ejection fraction. This finding may shed light on the numerous factors governing the pathophysiology of CHF. Public Library of Science 2008-09-18 /pmc/articles/PMC2528948/ /pubmed/18800166 http://dx.doi.org/10.1371/journal.pone.0003238 Text en Geft et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Geft, Dael
Schwartzenberg, Shmuel
Rogowsky, Ori
Finkelstein, Ariel
Ablin, Jacob
Maysel-Auslender, Sofia
Wexler, Dov
Keren, Gad
George, Jacob
Circulating Apoptotic Progenitor Cells in Patients with Congestive Heart Failure
title Circulating Apoptotic Progenitor Cells in Patients with Congestive Heart Failure
title_full Circulating Apoptotic Progenitor Cells in Patients with Congestive Heart Failure
title_fullStr Circulating Apoptotic Progenitor Cells in Patients with Congestive Heart Failure
title_full_unstemmed Circulating Apoptotic Progenitor Cells in Patients with Congestive Heart Failure
title_short Circulating Apoptotic Progenitor Cells in Patients with Congestive Heart Failure
title_sort circulating apoptotic progenitor cells in patients with congestive heart failure
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2528948/
https://www.ncbi.nlm.nih.gov/pubmed/18800166
http://dx.doi.org/10.1371/journal.pone.0003238
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