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Characterization of Decellularized Human Pericardium for Tissue Engineering and Regenerative Medicine Applications

BACKGROUND: Pericardium tissue allograft can be used for surgical repair in several procedures. One of the tissue engineering strategies is the process of decellularization. This process decreases immunogenic response, but it may modify the natural extracellular matrix composition and behavior. OBJE...

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Autores principales: Wollmann, Luciana, Suss, Paula, Mendonça, João, Luzia, Cesar, Schittini, Andressa, da Rosa, George Willian Xavier, Costa, Francisco, Tuon, Felipe F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Cardiologia - SBC 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6684174/
https://www.ncbi.nlm.nih.gov/pubmed/31271596
http://dx.doi.org/10.5935/abc.20190094
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author Wollmann, Luciana
Suss, Paula
Mendonça, João
Luzia, Cesar
Schittini, Andressa
da Rosa, George Willian Xavier
Costa, Francisco
Tuon, Felipe F.
author_facet Wollmann, Luciana
Suss, Paula
Mendonça, João
Luzia, Cesar
Schittini, Andressa
da Rosa, George Willian Xavier
Costa, Francisco
Tuon, Felipe F.
author_sort Wollmann, Luciana
collection PubMed
description BACKGROUND: Pericardium tissue allograft can be used for surgical repair in several procedures. One of the tissue engineering strategies is the process of decellularization. This process decreases immunogenic response, but it may modify the natural extracellular matrix composition and behavior. OBJECTIVE: The aim of this study was to evaluate the effectiveness of cell removal, maintenance of extracellular matrix properties and mechanical integrity of decellularized human pericardium using a low concentration solution of sodium dodecyl sulfate. METHODS: Decellularization was performed with sodium dodecyl sulfate and ethylenediaminetetraacetic acid. Histological analysis, DNA quantification, evaluation of glycosaminoglycans and collagen were performed. Biomechanical assay was performed using tensile test to compare the decellularization effects on tissue properties of tensile strength, elongation and elastic modulus. P < 0.05 was considered significant. RESULTS: There was reduction in visible nuclei present in pericardium tissue after decellularization, but it retained collagen and elastin bundles similar to fresh pericardium. The DNA contents of the decellularized pericardium were significantly reduced to less than 511.23 ± 120.4 ng per mg of dry weight (p < 0.001). The biomechanical assay showed no significant difference for fresh or decellularized tissue. CONCLUSION: The decellularization process reduces cell content as well as extracellular matrix components without changing its biomechanical properties.
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spelling pubmed-66841742019-08-28 Characterization of Decellularized Human Pericardium for Tissue Engineering and Regenerative Medicine Applications Wollmann, Luciana Suss, Paula Mendonça, João Luzia, Cesar Schittini, Andressa da Rosa, George Willian Xavier Costa, Francisco Tuon, Felipe F. Arq Bras Cardiol Original Article BACKGROUND: Pericardium tissue allograft can be used for surgical repair in several procedures. One of the tissue engineering strategies is the process of decellularization. This process decreases immunogenic response, but it may modify the natural extracellular matrix composition and behavior. OBJECTIVE: The aim of this study was to evaluate the effectiveness of cell removal, maintenance of extracellular matrix properties and mechanical integrity of decellularized human pericardium using a low concentration solution of sodium dodecyl sulfate. METHODS: Decellularization was performed with sodium dodecyl sulfate and ethylenediaminetetraacetic acid. Histological analysis, DNA quantification, evaluation of glycosaminoglycans and collagen were performed. Biomechanical assay was performed using tensile test to compare the decellularization effects on tissue properties of tensile strength, elongation and elastic modulus. P < 0.05 was considered significant. RESULTS: There was reduction in visible nuclei present in pericardium tissue after decellularization, but it retained collagen and elastin bundles similar to fresh pericardium. The DNA contents of the decellularized pericardium were significantly reduced to less than 511.23 ± 120.4 ng per mg of dry weight (p < 0.001). The biomechanical assay showed no significant difference for fresh or decellularized tissue. CONCLUSION: The decellularization process reduces cell content as well as extracellular matrix components without changing its biomechanical properties. Sociedade Brasileira de Cardiologia - SBC 2019-07 /pmc/articles/PMC6684174/ /pubmed/31271596 http://dx.doi.org/10.5935/abc.20190094 Text en 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 work is properly cited.
spellingShingle Original Article
Wollmann, Luciana
Suss, Paula
Mendonça, João
Luzia, Cesar
Schittini, Andressa
da Rosa, George Willian Xavier
Costa, Francisco
Tuon, Felipe F.
Characterization of Decellularized Human Pericardium for Tissue Engineering and Regenerative Medicine Applications
title Characterization of Decellularized Human Pericardium for Tissue Engineering and Regenerative Medicine Applications
title_full Characterization of Decellularized Human Pericardium for Tissue Engineering and Regenerative Medicine Applications
title_fullStr Characterization of Decellularized Human Pericardium for Tissue Engineering and Regenerative Medicine Applications
title_full_unstemmed Characterization of Decellularized Human Pericardium for Tissue Engineering and Regenerative Medicine Applications
title_short Characterization of Decellularized Human Pericardium for Tissue Engineering and Regenerative Medicine Applications
title_sort characterization of decellularized human pericardium for tissue engineering and regenerative medicine applications
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6684174/
https://www.ncbi.nlm.nih.gov/pubmed/31271596
http://dx.doi.org/10.5935/abc.20190094
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