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Release of soluble vascular endothelial growth factor receptor-1 (sFlt-1) during coronary artery bypass surgery
BACKGROUND: This study was conducted to follow plasma concentrations of sFlt-1 and sKDR, two soluble forms of the vascular endothelial growth factor (VEGF) receptor in patients undergoing coronary artery bypass graft (CABG) surgery with extracorporeal circulation (ECC). METHODS: Plasma samples were...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034558/ https://www.ncbi.nlm.nih.gov/pubmed/17888151 http://dx.doi.org/10.1186/1749-8090-2-38 |
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author | Denizot, Yves Leguyader, Alexandre Cornu, Elisabeth Laskar, Marc Orsel, Isabelle Vincent, Christelle Nathan, Nathalie |
author_facet | Denizot, Yves Leguyader, Alexandre Cornu, Elisabeth Laskar, Marc Orsel, Isabelle Vincent, Christelle Nathan, Nathalie |
author_sort | Denizot, Yves |
collection | PubMed |
description | BACKGROUND: This study was conducted to follow plasma concentrations of sFlt-1 and sKDR, two soluble forms of the vascular endothelial growth factor (VEGF) receptor in patients undergoing coronary artery bypass graft (CABG) surgery with extracorporeal circulation (ECC). METHODS: Plasma samples were obtained before, during and after surgery in 15 patients scheduled to undergo CABG. Levels of sFlt-1 and KDR levels were investigated using specific ELISA. RESULTS: A 75-fold increase of sFlt-1 was found during cardiac surgery, sFlt-1 levels returning to pre-operative values at the 6(th )post-operative hour. In contrast sKDR levels did not change during surgery. The ECC-derived sFlt-1 was functional as judge by its inhibitory effect on the VEGF mitogenic response in human umbilical vein endothelial cells (HUVECs). Kinetic experiments revealed sFlt-1 release immediately after the beginning of ECC suggesting a proteolysis of its membrane form (mFlt-1) rather than an elevated transcription/translation process. Flow cytometry analysis highlighted no effect of ECC on the shedding of mFlt-1 on platelets and leukocytes suggesting vascular endothelial cell as a putative cell source for the ECC-derived sFlt-1. CONCLUSION: sFlt-1 is released during CABG with ECC. It might be suggested that sFlt-1 production, by neutralizing VEGF and/or by inactivating membrane-bound Flt-1 and KDR receptors, might play a role in the occurrence of post-CABG complication. |
format | Text |
id | pubmed-2034558 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-20345582007-10-19 Release of soluble vascular endothelial growth factor receptor-1 (sFlt-1) during coronary artery bypass surgery Denizot, Yves Leguyader, Alexandre Cornu, Elisabeth Laskar, Marc Orsel, Isabelle Vincent, Christelle Nathan, Nathalie J Cardiothorac Surg Research Article BACKGROUND: This study was conducted to follow plasma concentrations of sFlt-1 and sKDR, two soluble forms of the vascular endothelial growth factor (VEGF) receptor in patients undergoing coronary artery bypass graft (CABG) surgery with extracorporeal circulation (ECC). METHODS: Plasma samples were obtained before, during and after surgery in 15 patients scheduled to undergo CABG. Levels of sFlt-1 and KDR levels were investigated using specific ELISA. RESULTS: A 75-fold increase of sFlt-1 was found during cardiac surgery, sFlt-1 levels returning to pre-operative values at the 6(th )post-operative hour. In contrast sKDR levels did not change during surgery. The ECC-derived sFlt-1 was functional as judge by its inhibitory effect on the VEGF mitogenic response in human umbilical vein endothelial cells (HUVECs). Kinetic experiments revealed sFlt-1 release immediately after the beginning of ECC suggesting a proteolysis of its membrane form (mFlt-1) rather than an elevated transcription/translation process. Flow cytometry analysis highlighted no effect of ECC on the shedding of mFlt-1 on platelets and leukocytes suggesting vascular endothelial cell as a putative cell source for the ECC-derived sFlt-1. CONCLUSION: sFlt-1 is released during CABG with ECC. It might be suggested that sFlt-1 production, by neutralizing VEGF and/or by inactivating membrane-bound Flt-1 and KDR receptors, might play a role in the occurrence of post-CABG complication. BioMed Central 2007-09-21 /pmc/articles/PMC2034558/ /pubmed/17888151 http://dx.doi.org/10.1186/1749-8090-2-38 Text en Copyright © 2007 Denizot et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Denizot, Yves Leguyader, Alexandre Cornu, Elisabeth Laskar, Marc Orsel, Isabelle Vincent, Christelle Nathan, Nathalie Release of soluble vascular endothelial growth factor receptor-1 (sFlt-1) during coronary artery bypass surgery |
title | Release of soluble vascular endothelial growth factor receptor-1 (sFlt-1) during coronary artery bypass surgery |
title_full | Release of soluble vascular endothelial growth factor receptor-1 (sFlt-1) during coronary artery bypass surgery |
title_fullStr | Release of soluble vascular endothelial growth factor receptor-1 (sFlt-1) during coronary artery bypass surgery |
title_full_unstemmed | Release of soluble vascular endothelial growth factor receptor-1 (sFlt-1) during coronary artery bypass surgery |
title_short | Release of soluble vascular endothelial growth factor receptor-1 (sFlt-1) during coronary artery bypass surgery |
title_sort | release of soluble vascular endothelial growth factor receptor-1 (sflt-1) during coronary artery bypass surgery |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2034558/ https://www.ncbi.nlm.nih.gov/pubmed/17888151 http://dx.doi.org/10.1186/1749-8090-2-38 |
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