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Nucleotide Catabolism on the Surface of Aortic Valve Xenografts; Effects of Different Decellularization Strategies
Extracellular nucleotide metabolism controls thrombosis and inflammation and may affect degeneration and calcification of aortic valve prostheses. We evaluated the effect of different decellularization strategies on enzyme activities involved in extracellular nucleotide metabolism. Porcine valves we...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830859/ https://www.ncbi.nlm.nih.gov/pubmed/26832118 http://dx.doi.org/10.1007/s12265-016-9672-6 |
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author | Kutryb-Zajac, Barbara Yuen, Ada H. Y. Khalpey, Zain Zukowska, Paulina Slominska, Ewa M. Taylor, Patricia M. Goldstein, Steven Heacox, Albert E. Lavitrano, Marialuisa Chester, Adrian H. Yacoub, Magdi H. Smolenski, Ryszard T. |
author_facet | Kutryb-Zajac, Barbara Yuen, Ada H. Y. Khalpey, Zain Zukowska, Paulina Slominska, Ewa M. Taylor, Patricia M. Goldstein, Steven Heacox, Albert E. Lavitrano, Marialuisa Chester, Adrian H. Yacoub, Magdi H. Smolenski, Ryszard T. |
author_sort | Kutryb-Zajac, Barbara |
collection | PubMed |
description | Extracellular nucleotide metabolism controls thrombosis and inflammation and may affect degeneration and calcification of aortic valve prostheses. We evaluated the effect of different decellularization strategies on enzyme activities involved in extracellular nucleotide metabolism. Porcine valves were tested intact or decellularized either by detergent treatment or hypotonic lysis and nuclease digestion. The rates of ATP hydrolysis, AMP hydrolysis, and adenosine deamination were estimated by incubation of aorta or valve leaflet sections with substrates followed by HPLC analysis. We demonstrated relatively high activities of ecto-enzymes on porcine valve as compared to the aortic wall. Hypotonic lysis/nuclease digestion preserved >80 % of ATP and AMP hydrolytic activity but reduced adenosine deamination to <10 %. Detergent decellularization completely removed (<5 %) all these activities. These results demonstrate high intensity of extracellular nucleotide metabolism on valve surface and indicate that various valve decellularization techniques differently affect ecto-enzyme activities that could be important in the development of improved valve prostheses. |
format | Online Article Text |
id | pubmed-4830859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-48308592016-04-22 Nucleotide Catabolism on the Surface of Aortic Valve Xenografts; Effects of Different Decellularization Strategies Kutryb-Zajac, Barbara Yuen, Ada H. Y. Khalpey, Zain Zukowska, Paulina Slominska, Ewa M. Taylor, Patricia M. Goldstein, Steven Heacox, Albert E. Lavitrano, Marialuisa Chester, Adrian H. Yacoub, Magdi H. Smolenski, Ryszard T. J Cardiovasc Transl Res Original Article Extracellular nucleotide metabolism controls thrombosis and inflammation and may affect degeneration and calcification of aortic valve prostheses. We evaluated the effect of different decellularization strategies on enzyme activities involved in extracellular nucleotide metabolism. Porcine valves were tested intact or decellularized either by detergent treatment or hypotonic lysis and nuclease digestion. The rates of ATP hydrolysis, AMP hydrolysis, and adenosine deamination were estimated by incubation of aorta or valve leaflet sections with substrates followed by HPLC analysis. We demonstrated relatively high activities of ecto-enzymes on porcine valve as compared to the aortic wall. Hypotonic lysis/nuclease digestion preserved >80 % of ATP and AMP hydrolytic activity but reduced adenosine deamination to <10 %. Detergent decellularization completely removed (<5 %) all these activities. These results demonstrate high intensity of extracellular nucleotide metabolism on valve surface and indicate that various valve decellularization techniques differently affect ecto-enzyme activities that could be important in the development of improved valve prostheses. Springer US 2016-02-01 2016 /pmc/articles/PMC4830859/ /pubmed/26832118 http://dx.doi.org/10.1007/s12265-016-9672-6 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Original Article Kutryb-Zajac, Barbara Yuen, Ada H. Y. Khalpey, Zain Zukowska, Paulina Slominska, Ewa M. Taylor, Patricia M. Goldstein, Steven Heacox, Albert E. Lavitrano, Marialuisa Chester, Adrian H. Yacoub, Magdi H. Smolenski, Ryszard T. Nucleotide Catabolism on the Surface of Aortic Valve Xenografts; Effects of Different Decellularization Strategies |
title | Nucleotide Catabolism on the Surface of Aortic Valve Xenografts; Effects of Different Decellularization Strategies |
title_full | Nucleotide Catabolism on the Surface of Aortic Valve Xenografts; Effects of Different Decellularization Strategies |
title_fullStr | Nucleotide Catabolism on the Surface of Aortic Valve Xenografts; Effects of Different Decellularization Strategies |
title_full_unstemmed | Nucleotide Catabolism on the Surface of Aortic Valve Xenografts; Effects of Different Decellularization Strategies |
title_short | Nucleotide Catabolism on the Surface of Aortic Valve Xenografts; Effects of Different Decellularization Strategies |
title_sort | nucleotide catabolism on the surface of aortic valve xenografts; effects of different decellularization strategies |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4830859/ https://www.ncbi.nlm.nih.gov/pubmed/26832118 http://dx.doi.org/10.1007/s12265-016-9672-6 |
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