Quantification of adhesion of mesenchymal stem cells spread on decellularized vein scaffold

Detalhes bibliográficos
Autor(a) principal: Rodrigues, Lenize da Silva [UNESP]
Data de Publicação: 2021
Outros Autores: Bovolato, Ana Lívia de Carvalho [UNESP], Silva, Bárbara Esteves [UNESP], Chizzolini, Leticia Victória [UNESP], da Cruz, Bianca Latance [UNESP], Moraes, Marcelo Padovani de Toledo [UNESP], Lourenção, Pedro Luiz Toledo de Arruda [UNESP], Bertanha, Matheus [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/ACB361001
http://hdl.handle.net/11449/229869
Resumo: Purpose: To evaluate methods that improve adipose-derived stem cells (ASCs) population in decellularized biological venous scaffold for tissue engineering in blood vessels, a model in rabbits. Methods: The ASC was expanded until the third passage. Inferior vena cava (IVC) was submitted to the decellularization process using 1% sodium dodecyl sulfate (SDS) or 2% sodium deoxycholate (SD) to compose 12 study groups (G): pure SD or SDS, exposed or not to 1% TritonX-100 (TX-100) and exposed or not to poly-l’lysine and laminin (PL). Scaffolds were covered with 1 × 105 or 1 × 106 ASCs diluted in 10 μL Puramatrix™. The histological analysis was done by cell counting in hematoxylin and eosin (HE) and nuclei count in immunofluorescence (IF) with 4’,6-Diamidine-2’-phenylindole dihydrochloride (DAPI). Results: The study of groups in HE and IF showed similar results. For both analyses, IVC-SD-1 × 106 ASC and IVC-SD-PL-1 × 106 ASC provided the best results. The IF technique showed better sensitivity than HE, with a weak agreement between them. Conclusion: Decellularizing agent and the number of ASC influence scaffolds cellularization response and the best protocols as those ones using SD with or without the addition of PL.
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spelling Quantification of adhesion of mesenchymal stem cells spread on decellularized vein scaffoldBlood vesselsEndotheliumMesenchymal stem cellsPeripheral arterial diseasePurpose: To evaluate methods that improve adipose-derived stem cells (ASCs) population in decellularized biological venous scaffold for tissue engineering in blood vessels, a model in rabbits. Methods: The ASC was expanded until the third passage. Inferior vena cava (IVC) was submitted to the decellularization process using 1% sodium dodecyl sulfate (SDS) or 2% sodium deoxycholate (SD) to compose 12 study groups (G): pure SD or SDS, exposed or not to 1% TritonX-100 (TX-100) and exposed or not to poly-l’lysine and laminin (PL). Scaffolds were covered with 1 × 105 or 1 × 106 ASCs diluted in 10 μL Puramatrix™. The histological analysis was done by cell counting in hematoxylin and eosin (HE) and nuclei count in immunofluorescence (IF) with 4’,6-Diamidine-2’-phenylindole dihydrochloride (DAPI). Results: The study of groups in HE and IF showed similar results. For both analyses, IVC-SD-1 × 106 ASC and IVC-SD-PL-1 × 106 ASC provided the best results. The IF technique showed better sensitivity than HE, with a weak agreement between them. Conclusion: Decellularizing agent and the number of ASC influence scaffolds cellularization response and the best protocols as those ones using SD with or without the addition of PL.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Department of Surgery and Orthopedics-Botucatu Medical School Universidade Estadual Paulista (UNESP)Botucatu Institute of Biosciences-Cell Engineering Laboratory-Botucatu Medical School-Universidade Estadual Paulista (UNESP)Botucatu Medical School Universidade Estadual Paulista (UNESP)Department of Pathology-Botucatu Medical School-Universidade Estadual Paulista (UNESP)Department of Surgery and Orthopedics-Botucatu Medical School Universidade Estadual Paulista (UNESP)Botucatu Institute of Biosciences-Cell Engineering Laboratory-Botucatu Medical School-Universidade Estadual Paulista (UNESP)Botucatu Medical School Universidade Estadual Paulista (UNESP)Department of Pathology-Botucatu Medical School-Universidade Estadual Paulista (UNESP)CAPES: 88882.433190/2019-01Universidade Estadual Paulista (UNESP)Rodrigues, Lenize da Silva [UNESP]Bovolato, Ana Lívia de Carvalho [UNESP]Silva, Bárbara Esteves [UNESP]Chizzolini, Leticia Victória [UNESP]da Cruz, Bianca Latance [UNESP]Moraes, Marcelo Padovani de Toledo [UNESP]Lourenção, Pedro Luiz Toledo de Arruda [UNESP]Bertanha, Matheus [UNESP]2022-04-29T08:36:18Z2022-04-29T08:36:18Z2021-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://dx.doi.org/10.1590/ACB361001Acta Cirurgica Brasileira, v. 36, n. 10, 2021.1678-26740102-8650http://hdl.handle.net/11449/22986910.1590/ACB3610012-s2.0-85118926769Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengActa Cirurgica Brasileirainfo:eu-repo/semantics/openAccess2024-09-03T13:18:32Zoai:repositorio.unesp.br:11449/229869Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-03T13:18:32Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Quantification of adhesion of mesenchymal stem cells spread on decellularized vein scaffold
title Quantification of adhesion of mesenchymal stem cells spread on decellularized vein scaffold
spellingShingle Quantification of adhesion of mesenchymal stem cells spread on decellularized vein scaffold
Rodrigues, Lenize da Silva [UNESP]
Blood vessels
Endothelium
Mesenchymal stem cells
Peripheral arterial disease
title_short Quantification of adhesion of mesenchymal stem cells spread on decellularized vein scaffold
title_full Quantification of adhesion of mesenchymal stem cells spread on decellularized vein scaffold
title_fullStr Quantification of adhesion of mesenchymal stem cells spread on decellularized vein scaffold
title_full_unstemmed Quantification of adhesion of mesenchymal stem cells spread on decellularized vein scaffold
title_sort Quantification of adhesion of mesenchymal stem cells spread on decellularized vein scaffold
author Rodrigues, Lenize da Silva [UNESP]
author_facet Rodrigues, Lenize da Silva [UNESP]
Bovolato, Ana Lívia de Carvalho [UNESP]
Silva, Bárbara Esteves [UNESP]
Chizzolini, Leticia Victória [UNESP]
da Cruz, Bianca Latance [UNESP]
Moraes, Marcelo Padovani de Toledo [UNESP]
Lourenção, Pedro Luiz Toledo de Arruda [UNESP]
Bertanha, Matheus [UNESP]
author_role author
author2 Bovolato, Ana Lívia de Carvalho [UNESP]
Silva, Bárbara Esteves [UNESP]
Chizzolini, Leticia Victória [UNESP]
da Cruz, Bianca Latance [UNESP]
Moraes, Marcelo Padovani de Toledo [UNESP]
Lourenção, Pedro Luiz Toledo de Arruda [UNESP]
Bertanha, Matheus [UNESP]
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
dc.contributor.author.fl_str_mv Rodrigues, Lenize da Silva [UNESP]
Bovolato, Ana Lívia de Carvalho [UNESP]
Silva, Bárbara Esteves [UNESP]
Chizzolini, Leticia Victória [UNESP]
da Cruz, Bianca Latance [UNESP]
Moraes, Marcelo Padovani de Toledo [UNESP]
Lourenção, Pedro Luiz Toledo de Arruda [UNESP]
Bertanha, Matheus [UNESP]
dc.subject.por.fl_str_mv Blood vessels
Endothelium
Mesenchymal stem cells
Peripheral arterial disease
topic Blood vessels
Endothelium
Mesenchymal stem cells
Peripheral arterial disease
description Purpose: To evaluate methods that improve adipose-derived stem cells (ASCs) population in decellularized biological venous scaffold for tissue engineering in blood vessels, a model in rabbits. Methods: The ASC was expanded until the third passage. Inferior vena cava (IVC) was submitted to the decellularization process using 1% sodium dodecyl sulfate (SDS) or 2% sodium deoxycholate (SD) to compose 12 study groups (G): pure SD or SDS, exposed or not to 1% TritonX-100 (TX-100) and exposed or not to poly-l’lysine and laminin (PL). Scaffolds were covered with 1 × 105 or 1 × 106 ASCs diluted in 10 μL Puramatrix™. The histological analysis was done by cell counting in hematoxylin and eosin (HE) and nuclei count in immunofluorescence (IF) with 4’,6-Diamidine-2’-phenylindole dihydrochloride (DAPI). Results: The study of groups in HE and IF showed similar results. For both analyses, IVC-SD-1 × 106 ASC and IVC-SD-PL-1 × 106 ASC provided the best results. The IF technique showed better sensitivity than HE, with a weak agreement between them. Conclusion: Decellularizing agent and the number of ASC influence scaffolds cellularization response and the best protocols as those ones using SD with or without the addition of PL.
publishDate 2021
dc.date.none.fl_str_mv 2021-01-01
2022-04-29T08:36:18Z
2022-04-29T08:36:18Z
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/10.1590/ACB361001
Acta Cirurgica Brasileira, v. 36, n. 10, 2021.
1678-2674
0102-8650
http://hdl.handle.net/11449/229869
10.1590/ACB361001
2-s2.0-85118926769
url http://dx.doi.org/10.1590/ACB361001
http://hdl.handle.net/11449/229869
identifier_str_mv Acta Cirurgica Brasileira, v. 36, n. 10, 2021.
1678-2674
0102-8650
10.1590/ACB361001
2-s2.0-85118926769
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Acta Cirurgica Brasileira
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.source.none.fl_str_mv Scopus
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
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