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Serum of obstructive sleep apnea patients impairs human coronary endothelial cell migration

INTRODUCTION: Endothelial cell migration and proliferation play an important role in the growth and development of new blood vessels and endothelium healing. This process occurs in response to injury, inflammation and immune reactions. Dysfunction of the endothelium may play a significant role in de...

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Autores principales: Hoffmann, Michał, Wolf, Jacek, Szyndler, Anna, Singh, Prachi, Somers, Virend K., Narkiewicz, Krzysztof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5206357/
https://www.ncbi.nlm.nih.gov/pubmed/28144275
http://dx.doi.org/10.5114/aoms.2015.56490
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author Hoffmann, Michał
Wolf, Jacek
Szyndler, Anna
Singh, Prachi
Somers, Virend K.
Narkiewicz, Krzysztof
author_facet Hoffmann, Michał
Wolf, Jacek
Szyndler, Anna
Singh, Prachi
Somers, Virend K.
Narkiewicz, Krzysztof
author_sort Hoffmann, Michał
collection PubMed
description INTRODUCTION: Endothelial cell migration and proliferation play an important role in the growth and development of new blood vessels and endothelium healing. This process occurs in response to injury, inflammation and immune reactions. Dysfunction of the endothelium may play a significant role in development and progression of cardiovascular disease related to sleep-disordered breathing. The aim of our study was to evaluate the chemo-attractant activity of serum from obstructive sleep apnea (OSA) and normal subjects on coronary artery endothelial cell migration. MATERIAL AND METHODS: We studied 12 severe OSA patients, free of other co-morbidities and on no treatment, along with 12 age-, body mass index, and gender matched healthy controls. Blood was collected at three time points: at 21:00 before sleep, at 6:00 after waking from sleep, and at 11:00 (after 5 h of normal daytime activity). Serum chemo-attractant activity for human coronary endothelial cells was assessed using a colorimetric cell migration assay kit. RESULTS: In healthy subjects, serum chemo-attractant activity peaked in the morning after waking from sleep (p = 0.02). This early morning increase was blunted in severe OSA subjects, in whom chemo-attractant activity was weaker than in normal controls (p = 0.02), and did not change significantly at the different time-points (p < 0.001 vs. controls). CONCLUSIONS: Chemo-attractant activity of the serum from OSA patients is lower compared to serum from healthy subjects, especially in the morning. Altered chemo-attractant serum activity may conceivably contribute to the impairment of endothelial function in obstructive sleep apnea patients.
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spelling pubmed-52063572017-02-01 Serum of obstructive sleep apnea patients impairs human coronary endothelial cell migration Hoffmann, Michał Wolf, Jacek Szyndler, Anna Singh, Prachi Somers, Virend K. Narkiewicz, Krzysztof Arch Med Sci Basic Research INTRODUCTION: Endothelial cell migration and proliferation play an important role in the growth and development of new blood vessels and endothelium healing. This process occurs in response to injury, inflammation and immune reactions. Dysfunction of the endothelium may play a significant role in development and progression of cardiovascular disease related to sleep-disordered breathing. The aim of our study was to evaluate the chemo-attractant activity of serum from obstructive sleep apnea (OSA) and normal subjects on coronary artery endothelial cell migration. MATERIAL AND METHODS: We studied 12 severe OSA patients, free of other co-morbidities and on no treatment, along with 12 age-, body mass index, and gender matched healthy controls. Blood was collected at three time points: at 21:00 before sleep, at 6:00 after waking from sleep, and at 11:00 (after 5 h of normal daytime activity). Serum chemo-attractant activity for human coronary endothelial cells was assessed using a colorimetric cell migration assay kit. RESULTS: In healthy subjects, serum chemo-attractant activity peaked in the morning after waking from sleep (p = 0.02). This early morning increase was blunted in severe OSA subjects, in whom chemo-attractant activity was weaker than in normal controls (p = 0.02), and did not change significantly at the different time-points (p < 0.001 vs. controls). CONCLUSIONS: Chemo-attractant activity of the serum from OSA patients is lower compared to serum from healthy subjects, especially in the morning. Altered chemo-attractant serum activity may conceivably contribute to the impairment of endothelial function in obstructive sleep apnea patients. Termedia Publishing House 2015-12-16 2017-02-01 /pmc/articles/PMC5206357/ /pubmed/28144275 http://dx.doi.org/10.5114/aoms.2015.56490 Text en Copyright: © 2015 Termedia & Banach http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Basic Research
Hoffmann, Michał
Wolf, Jacek
Szyndler, Anna
Singh, Prachi
Somers, Virend K.
Narkiewicz, Krzysztof
Serum of obstructive sleep apnea patients impairs human coronary endothelial cell migration
title Serum of obstructive sleep apnea patients impairs human coronary endothelial cell migration
title_full Serum of obstructive sleep apnea patients impairs human coronary endothelial cell migration
title_fullStr Serum of obstructive sleep apnea patients impairs human coronary endothelial cell migration
title_full_unstemmed Serum of obstructive sleep apnea patients impairs human coronary endothelial cell migration
title_short Serum of obstructive sleep apnea patients impairs human coronary endothelial cell migration
title_sort serum of obstructive sleep apnea patients impairs human coronary endothelial cell migration
topic Basic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5206357/
https://www.ncbi.nlm.nih.gov/pubmed/28144275
http://dx.doi.org/10.5114/aoms.2015.56490
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