Morphofunctional characterization of decellularized vena cava as tissue engineering scaffolds

Detalhes bibliográficos
Autor(a) principal: Bertanha, Matheus [UNESP]
Data de Publicação: 2014
Outros Autores: 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]
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.
id UNSP_a1c0a606dfc02d6e3189a8747fe8c1f3
oai_identifier_str oai:repositorio.unesp.br:11449/116798
network_acronym_str UNSP
network_name_str Repositório Institucional da UNESP
repository_id_str 2946
spelling 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