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Fibronectin coating of oxygenator membranes enhances endothelial cell attachment

BACKGROUND: Extracorporeal membrane oxygenation (ECMO) can replace the lungs’ gas exchange capacity in refractory lung failure. However, its limited hemocompatibility, the activation of the coagulation and complement system as well as plasma leakage and protein deposition hamper mid- to long-term us...

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Autores principales: Cornelissen, Christian G, Dietrich, Maren, Gromann, Kai, Frese, Julia, Krueger, Stefan, Sachweh, Jörg S, Jockenhoevel, Stefan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617998/
https://www.ncbi.nlm.nih.gov/pubmed/23356939
http://dx.doi.org/10.1186/1475-925X-12-7
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author Cornelissen, Christian G
Dietrich, Maren
Gromann, Kai
Frese, Julia
Krueger, Stefan
Sachweh, Jörg S
Jockenhoevel, Stefan
author_facet Cornelissen, Christian G
Dietrich, Maren
Gromann, Kai
Frese, Julia
Krueger, Stefan
Sachweh, Jörg S
Jockenhoevel, Stefan
author_sort Cornelissen, Christian G
collection PubMed
description BACKGROUND: Extracorporeal membrane oxygenation (ECMO) can replace the lungs’ gas exchange capacity in refractory lung failure. However, its limited hemocompatibility, the activation of the coagulation and complement system as well as plasma leakage and protein deposition hamper mid- to long-term use and have constrained the development of an implantable lung assist device. In a tissue engineering approach, lining the blood contact surfaces of the ECMO device with endothelial cells might overcome these limitations. As a first step towards this aim, we hypothesized that coating the oxygenator’s gas exchange membrane with proteins might positively influence the attachment and proliferation of arterial endothelial cells. METHODS: Sheets of polypropylene (PP), polyoxymethylpentene (TPX) and polydimethylsiloxane (PDMS), typical material used for oxygenator gas exchange membranes, were coated with collagen, fibrinogen, gelatin or fibronectin. Tissue culture treated well plates served as controls. Endothelial cell attachment and proliferation were analyzed for a period of 4 days by microscopic examination and computer assisted cell counting. RESULTS: Endothelial cell seeding efficiency is within range of tissue culture treated controls for fibronectin treated surfaces only. Uncoated membranes as well as all other coatings lead to lower cell attachment. A confluent endothelial cell layer develops on fibronectin coated PDMS and the control surface only. CONCLUSIONS: Fibronectin increases endothelial cells’ seeding efficiency on different oxygenator membrane material. PDMS coated with fibronectin shows sustained cell attachment for a period of four days in static culture conditions.
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spelling pubmed-36179982013-04-06 Fibronectin coating of oxygenator membranes enhances endothelial cell attachment Cornelissen, Christian G Dietrich, Maren Gromann, Kai Frese, Julia Krueger, Stefan Sachweh, Jörg S Jockenhoevel, Stefan Biomed Eng Online Research BACKGROUND: Extracorporeal membrane oxygenation (ECMO) can replace the lungs’ gas exchange capacity in refractory lung failure. However, its limited hemocompatibility, the activation of the coagulation and complement system as well as plasma leakage and protein deposition hamper mid- to long-term use and have constrained the development of an implantable lung assist device. In a tissue engineering approach, lining the blood contact surfaces of the ECMO device with endothelial cells might overcome these limitations. As a first step towards this aim, we hypothesized that coating the oxygenator’s gas exchange membrane with proteins might positively influence the attachment and proliferation of arterial endothelial cells. METHODS: Sheets of polypropylene (PP), polyoxymethylpentene (TPX) and polydimethylsiloxane (PDMS), typical material used for oxygenator gas exchange membranes, were coated with collagen, fibrinogen, gelatin or fibronectin. Tissue culture treated well plates served as controls. Endothelial cell attachment and proliferation were analyzed for a period of 4 days by microscopic examination and computer assisted cell counting. RESULTS: Endothelial cell seeding efficiency is within range of tissue culture treated controls for fibronectin treated surfaces only. Uncoated membranes as well as all other coatings lead to lower cell attachment. A confluent endothelial cell layer develops on fibronectin coated PDMS and the control surface only. CONCLUSIONS: Fibronectin increases endothelial cells’ seeding efficiency on different oxygenator membrane material. PDMS coated with fibronectin shows sustained cell attachment for a period of four days in static culture conditions. BioMed Central 2013-01-28 /pmc/articles/PMC3617998/ /pubmed/23356939 http://dx.doi.org/10.1186/1475-925X-12-7 Text en Copyright © 2013 Cornelissen 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
Cornelissen, Christian G
Dietrich, Maren
Gromann, Kai
Frese, Julia
Krueger, Stefan
Sachweh, Jörg S
Jockenhoevel, Stefan
Fibronectin coating of oxygenator membranes enhances endothelial cell attachment
title Fibronectin coating of oxygenator membranes enhances endothelial cell attachment
title_full Fibronectin coating of oxygenator membranes enhances endothelial cell attachment
title_fullStr Fibronectin coating of oxygenator membranes enhances endothelial cell attachment
title_full_unstemmed Fibronectin coating of oxygenator membranes enhances endothelial cell attachment
title_short Fibronectin coating of oxygenator membranes enhances endothelial cell attachment
title_sort fibronectin coating of oxygenator membranes enhances endothelial cell attachment
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3617998/
https://www.ncbi.nlm.nih.gov/pubmed/23356939
http://dx.doi.org/10.1186/1475-925X-12-7
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