Quantification of adhesion of mesenchymal stem cells spread on decellularized vein scaffold
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Outros Autores: | , , , , , , |
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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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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1810021415995310080 |