Morphofunctional characterization of decellularized vena cava as tissue engineering scaffolds
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNESP |
Texto Completo: | http://dx.doi.org/10.1016/j.yexcr.2014.05.023 http://hdl.handle.net/11449/116798 |
Resumo: | Clinical experience for peripheral arterial disease treatment shows poor results when synthetic grafts are used to approach infrapopliteal arterial segments. However, tissue engineering may be an option to yield surrogate biocompatible neovessels. Thus, biological decellularized scaffolds could provide natural tissue architecture to use in tissue engineering, when the absence of ideal autologous veins reduces surgical options. The goal of this study was to evaluate different chemical induced decellularization protocols of the inferior vena cava of rabbits. They were decellularized with Triton X100 (TX100), sodium dodecyl sulfate (SDS) or sodium deoxycholate (DS). Afterwards, we assessed the remaining extracellular matrix (ECM) integrity, residual toxicity and the biomechanical resistance of the scaffolds. Our results showed that TX100 was not effective to remove the cells, while protocols using SDS 1% for 2 h and DS 2% for 1 h, efficiently removed the cells and were better characterized. These scaffolds preserved the original organization of ECM. In addition, the residual toxicity assessment did not reveal statistically significant changes while decellularized scaffolds retained the equivalent biomechanical properties when compared with the control. Our results concluded that protocols using SDS and DS were effective at obtaining decellularized scaffolds, which may be useful for blood vessel tissue engineering. (C) 2014 Published by Elsevier Inc. |
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Morphofunctional characterization of decellularized vena cava as tissue engineering scaffoldsPeripheral arterial diseaseBlood vesselsTissue engineeringBiomechanicsExtracellular matrixClinical experience for peripheral arterial disease treatment shows poor results when synthetic grafts are used to approach infrapopliteal arterial segments. However, tissue engineering may be an option to yield surrogate biocompatible neovessels. Thus, biological decellularized scaffolds could provide natural tissue architecture to use in tissue engineering, when the absence of ideal autologous veins reduces surgical options. The goal of this study was to evaluate different chemical induced decellularization protocols of the inferior vena cava of rabbits. They were decellularized with Triton X100 (TX100), sodium dodecyl sulfate (SDS) or sodium deoxycholate (DS). Afterwards, we assessed the remaining extracellular matrix (ECM) integrity, residual toxicity and the biomechanical resistance of the scaffolds. Our results showed that TX100 was not effective to remove the cells, while protocols using SDS 1% for 2 h and DS 2% for 1 h, efficiently removed the cells and were better characterized. These scaffolds preserved the original organization of ECM. In addition, the residual toxicity assessment did not reveal statistically significant changes while decellularized scaffolds retained the equivalent biomechanical properties when compared with the control. Our results concluded that protocols using SDS and DS were effective at obtaining decellularized scaffolds, which may be useful for blood vessel tissue engineering. (C) 2014 Published by Elsevier Inc.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Sao Paulo State Univ UNESP, Botucatu Med Sch, Dept Surg & Orthoped, Vasc Lab, BR-18618970 Botucatu, SP, BrazilSao Paulo State Univ UNESP, Botucatu Med Sch, Cell Engn Lab, Blood Transfus Ctr, Botucatu, SP, BrazilSao Paulo State Univ, Sch Pharmaceut Sci, Dept Bioproc & Biotechnol, Araraquara, SP, BrazilSao Paulo State Univ, Botucatu Biosci Inst, Extracellular Matrix Lab, Dept Morphol, Botucatu, SP, BrazilSao Paulo State Univ UNESP, Botucatu Med Sch, Flow Cytometry Lab, Ctr Blood Transfus, Botucatu, SP, BrazilSao Paulo State Univ, Botucatu Med Sch, Immunohistochem Lab, Dept Pathol, Botucatu, SP, BrazilScio Paulo State Univ UNESP, Botucatu Med Sch, Dept Urol, Botucatu, SP, BrazilSao Paulo State Univ UNESP, Botucatu Med Sch, Dept Surg & Orthoped, Vasc Lab, BR-18618970 Botucatu, SP, BrazilSao Paulo State Univ UNESP, Botucatu Med Sch, Cell Engn Lab, Blood Transfus Ctr, Botucatu, SP, BrazilSao Paulo State Univ, Sch Pharmaceut Sci, Dept Bioproc & Biotechnol, Araraquara, SP, BrazilSao Paulo State Univ, Botucatu Biosci Inst, Extracellular Matrix Lab, Dept Morphol, Botucatu, SP, BrazilSao Paulo State Univ UNESP, Botucatu Med Sch, Flow Cytometry Lab, Ctr Blood Transfus, Botucatu, SP, BrazilSao Paulo State Univ, Botucatu Med Sch, Immunohistochem Lab, Dept Pathol, Botucatu, SP, BrazilScio Paulo State Univ UNESP, Botucatu Med Sch, Dept Urol, Botucatu, SP, BrazilFAPESP: 10/52549-8Elsevier B.V.Universidade Estadual Paulista (Unesp)Bertanha, Matheus [UNESP]Moroz, Andrei[UNESP]Jaldin, Rodrigo G. [UNESP]Silva, Regina A. M. [UNESP]Rinaldi, Jaqueline C. [UNESP]Golim, Márjorie de Assis [UNESP]Felisbino, Sergio L. [UNESP]Domingues, Maria Aparecida Custódio [UNESP]Sobreira, Marcone Lima [UNESP]Reis, Patricia Pintor dos [UNESP]Deffune, Elenice [UNESP]2015-03-18T15:54:10Z2015-03-18T15:54:10Z2014-08-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article103-111application/pdfhttp://dx.doi.org/10.1016/j.yexcr.2014.05.023Experimental Cell Research. San Diego: Elsevier Inc, v. 326, n. 1, p. 103-111, 2014.0014-4827http://hdl.handle.net/11449/11679810.1016/j.yexcr.2014.05.023WOS:000339704600010WOS000339704600010.pdf110952502163101196467640713392149609324832591382058572311303714045130143794613830000-0003-3775-3797Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengExperimental Cell Research3.3091,583info:eu-repo/semantics/openAccess2024-09-03T14:30:11Zoai:repositorio.unesp.br:11449/116798Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-03T14:30:11Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false |
dc.title.none.fl_str_mv |
Morphofunctional characterization of decellularized vena cava as tissue engineering scaffolds |
title |
Morphofunctional characterization of decellularized vena cava as tissue engineering scaffolds |
spellingShingle |
Morphofunctional characterization of decellularized vena cava as tissue engineering scaffolds Bertanha, Matheus [UNESP] Peripheral arterial disease Blood vessels Tissue engineering Biomechanics Extracellular matrix |
title_short |
Morphofunctional characterization of decellularized vena cava as tissue engineering scaffolds |
title_full |
Morphofunctional characterization of decellularized vena cava as tissue engineering scaffolds |
title_fullStr |
Morphofunctional characterization of decellularized vena cava as tissue engineering scaffolds |
title_full_unstemmed |
Morphofunctional characterization of decellularized vena cava as tissue engineering scaffolds |
title_sort |
Morphofunctional characterization of decellularized vena cava as tissue engineering scaffolds |
author |
Bertanha, Matheus [UNESP] |
author_facet |
Bertanha, Matheus [UNESP] Moroz, Andrei[UNESP] Jaldin, Rodrigo G. [UNESP] Silva, Regina A. M. [UNESP] Rinaldi, Jaqueline C. [UNESP] Golim, Márjorie de Assis [UNESP] Felisbino, Sergio L. [UNESP] Domingues, Maria Aparecida Custódio [UNESP] Sobreira, Marcone Lima [UNESP] Reis, Patricia Pintor dos [UNESP] Deffune, Elenice [UNESP] |
author_role |
author |
author2 |
Moroz, Andrei[UNESP] Jaldin, Rodrigo G. [UNESP] Silva, Regina A. M. [UNESP] Rinaldi, Jaqueline C. [UNESP] Golim, Márjorie de Assis [UNESP] Felisbino, Sergio L. [UNESP] Domingues, Maria Aparecida Custódio [UNESP] Sobreira, Marcone Lima [UNESP] Reis, Patricia Pintor dos [UNESP] Deffune, Elenice [UNESP] |
author2_role |
author author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Estadual Paulista (Unesp) |
dc.contributor.author.fl_str_mv |
Bertanha, Matheus [UNESP] Moroz, Andrei[UNESP] Jaldin, Rodrigo G. [UNESP] Silva, Regina A. M. [UNESP] Rinaldi, Jaqueline C. [UNESP] Golim, Márjorie de Assis [UNESP] Felisbino, Sergio L. [UNESP] Domingues, Maria Aparecida Custódio [UNESP] Sobreira, Marcone Lima [UNESP] Reis, Patricia Pintor dos [UNESP] Deffune, Elenice [UNESP] |
dc.subject.por.fl_str_mv |
Peripheral arterial disease Blood vessels Tissue engineering Biomechanics Extracellular matrix |
topic |
Peripheral arterial disease Blood vessels Tissue engineering Biomechanics Extracellular matrix |
description |
Clinical experience for peripheral arterial disease treatment shows poor results when synthetic grafts are used to approach infrapopliteal arterial segments. However, tissue engineering may be an option to yield surrogate biocompatible neovessels. Thus, biological decellularized scaffolds could provide natural tissue architecture to use in tissue engineering, when the absence of ideal autologous veins reduces surgical options. The goal of this study was to evaluate different chemical induced decellularization protocols of the inferior vena cava of rabbits. They were decellularized with Triton X100 (TX100), sodium dodecyl sulfate (SDS) or sodium deoxycholate (DS). Afterwards, we assessed the remaining extracellular matrix (ECM) integrity, residual toxicity and the biomechanical resistance of the scaffolds. Our results showed that TX100 was not effective to remove the cells, while protocols using SDS 1% for 2 h and DS 2% for 1 h, efficiently removed the cells and were better characterized. These scaffolds preserved the original organization of ECM. In addition, the residual toxicity assessment did not reveal statistically significant changes while decellularized scaffolds retained the equivalent biomechanical properties when compared with the control. Our results concluded that protocols using SDS and DS were effective at obtaining decellularized scaffolds, which may be useful for blood vessel tissue engineering. (C) 2014 Published by Elsevier Inc. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-08-01 2015-03-18T15:54:10Z 2015-03-18T15:54:10Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.yexcr.2014.05.023 Experimental Cell Research. San Diego: Elsevier Inc, v. 326, n. 1, p. 103-111, 2014. 0014-4827 http://hdl.handle.net/11449/116798 10.1016/j.yexcr.2014.05.023 WOS:000339704600010 WOS000339704600010.pdf 1109525021631011 9646764071339214 9609324832591382 0585723113037140 4513014379461383 0000-0003-3775-3797 |
url |
http://dx.doi.org/10.1016/j.yexcr.2014.05.023 http://hdl.handle.net/11449/116798 |
identifier_str_mv |
Experimental Cell Research. San Diego: Elsevier Inc, v. 326, n. 1, p. 103-111, 2014. 0014-4827 10.1016/j.yexcr.2014.05.023 WOS:000339704600010 WOS000339704600010.pdf 1109525021631011 9646764071339214 9609324832591382 0585723113037140 4513014379461383 0000-0003-3775-3797 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Experimental Cell Research 3.309 1,583 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
103-111 application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier B.V. |
publisher.none.fl_str_mv |
Elsevier B.V. |
dc.source.none.fl_str_mv |
Web of Science reponame:Repositório Institucional da UNESP instname:Universidade Estadual Paulista (UNESP) instacron:UNESP |
instname_str |
Universidade Estadual Paulista (UNESP) |
instacron_str |
UNESP |
institution |
UNESP |
reponame_str |
Repositório Institucional da UNESP |
collection |
Repositório Institucional da UNESP |
repository.name.fl_str_mv |
Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP) |
repository.mail.fl_str_mv |
repositoriounesp@unesp.br |
_version_ |
1810021385205972992 |