Phenotypic markers of oral keratinocytes seeded on two distinct 3D oral mucosa models

Detalhes bibliográficos
Autor(a) principal: Basso, Fernanda G. [UNESP]
Data de Publicação: 2018
Outros Autores: Pansani, Taisa N. [UNESP], Marcelo, Cyntia L., de Souza Costa, Carlos Alberto [UNESP], Hebling, Josimeri [UNESP], Feinberg, Stephen E.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.tiv.2018.04.015
http://hdl.handle.net/11449/179844
Resumo: This study validates the use of a full-thickness oral mucosa model for in vitro studies with a collagen type I matrix, by comparison of this model with two other 3D oral mucosa models: human-sourced and porcine acellular dermal matrices (AlloDerm®/Strattice®, respectively). For the collagen matrix model, gingival fibroblasts were seeded either onto the dermal side of the AlloDerm® and Strattice® matrices or within the collagen matrices in complete culture medium (DMEM). For all scaffolds, DMEM was replaced every 24 h up to 72 h. For the full-thickness oral mucosa models, 72 h after fibroblast seeding, oral keratinocytes were seeded on the epidermal sides of AlloDerm® and Strattice® matrices or collagen matrices. All matrices and models were subjected to histological analysis, complementing phenotypic characterization by evaluation of glucose consumption, cell proliferation, gene expression and synthesis of growth factors. A higher fibroblast ratio was observed for the collagen matrix, in which the distribution of gingival fibroblasts was also more homogeneous. Metabolism, proliferation, and gene expression and synthesis of VEGF of these cells were also increased for the collagen matrix. All matrices provided a suitable substrate for oral keratinocytes adhesion, proliferation, and phenotypic expression; however, higher proliferation, stratification, and differentiation were noted when oral keratinocytes were seeded on the dermal matrices.
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spelling Phenotypic markers of oral keratinocytes seeded on two distinct 3D oral mucosa modelsCell culture techniquesGingival fibroblastsOrganotypic cell cultureThis study validates the use of a full-thickness oral mucosa model for in vitro studies with a collagen type I matrix, by comparison of this model with two other 3D oral mucosa models: human-sourced and porcine acellular dermal matrices (AlloDerm®/Strattice®, respectively). For the collagen matrix model, gingival fibroblasts were seeded either onto the dermal side of the AlloDerm® and Strattice® matrices or within the collagen matrices in complete culture medium (DMEM). For all scaffolds, DMEM was replaced every 24 h up to 72 h. For the full-thickness oral mucosa models, 72 h after fibroblast seeding, oral keratinocytes were seeded on the epidermal sides of AlloDerm® and Strattice® matrices or collagen matrices. All matrices and models were subjected to histological analysis, complementing phenotypic characterization by evaluation of glucose consumption, cell proliferation, gene expression and synthesis of growth factors. A higher fibroblast ratio was observed for the collagen matrix, in which the distribution of gingival fibroblasts was also more homogeneous. Metabolism, proliferation, and gene expression and synthesis of VEGF of these cells were also increased for the collagen matrix. All matrices provided a suitable substrate for oral keratinocytes adhesion, proliferation, and phenotypic expression; however, higher proliferation, stratification, and differentiation were noted when oral keratinocytes were seeded on the dermal matrices.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Universidade Estadual Paulista (Unesp) Araraquara Dental SchoolUniversity of MichighanUniversidade Estadual Paulista (Unesp) Araraquara Dental SchoolFAPESP: 2012/17947-8FAPESP: 2013/05879-0FAPESP: 2014/06057-7Universidade Estadual Paulista (Unesp)University of MichighanBasso, Fernanda G. [UNESP]Pansani, Taisa N. [UNESP]Marcelo, Cyntia L.de Souza Costa, Carlos Alberto [UNESP]Hebling, Josimeri [UNESP]Feinberg, Stephen E.2018-12-11T17:36:59Z2018-12-11T17:36:59Z2018-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article34-39application/pdfhttp://dx.doi.org/10.1016/j.tiv.2018.04.015Toxicology in Vitro, v. 51, p. 34-39.1879-31770887-2333http://hdl.handle.net/11449/17984410.1016/j.tiv.2018.04.0152-s2.0-850466545212-s2.0-85046654521.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengToxicology in Vitro0,931info:eu-repo/semantics/openAccess2024-09-26T14:21:35Zoai:repositorio.unesp.br:11449/179844Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestrepositoriounesp@unesp.bropendoar:29462024-09-26T14:21:35Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Phenotypic markers of oral keratinocytes seeded on two distinct 3D oral mucosa models
title Phenotypic markers of oral keratinocytes seeded on two distinct 3D oral mucosa models
spellingShingle Phenotypic markers of oral keratinocytes seeded on two distinct 3D oral mucosa models
Basso, Fernanda G. [UNESP]
Cell culture techniques
Gingival fibroblasts
Organotypic cell culture
title_short Phenotypic markers of oral keratinocytes seeded on two distinct 3D oral mucosa models
title_full Phenotypic markers of oral keratinocytes seeded on two distinct 3D oral mucosa models
title_fullStr Phenotypic markers of oral keratinocytes seeded on two distinct 3D oral mucosa models
title_full_unstemmed Phenotypic markers of oral keratinocytes seeded on two distinct 3D oral mucosa models
title_sort Phenotypic markers of oral keratinocytes seeded on two distinct 3D oral mucosa models
author Basso, Fernanda G. [UNESP]
author_facet Basso, Fernanda G. [UNESP]
Pansani, Taisa N. [UNESP]
Marcelo, Cyntia L.
de Souza Costa, Carlos Alberto [UNESP]
Hebling, Josimeri [UNESP]
Feinberg, Stephen E.
author_role author
author2 Pansani, Taisa N. [UNESP]
Marcelo, Cyntia L.
de Souza Costa, Carlos Alberto [UNESP]
Hebling, Josimeri [UNESP]
Feinberg, Stephen E.
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
University of Michighan
dc.contributor.author.fl_str_mv Basso, Fernanda G. [UNESP]
Pansani, Taisa N. [UNESP]
Marcelo, Cyntia L.
de Souza Costa, Carlos Alberto [UNESP]
Hebling, Josimeri [UNESP]
Feinberg, Stephen E.
dc.subject.por.fl_str_mv Cell culture techniques
Gingival fibroblasts
Organotypic cell culture
topic Cell culture techniques
Gingival fibroblasts
Organotypic cell culture
description This study validates the use of a full-thickness oral mucosa model for in vitro studies with a collagen type I matrix, by comparison of this model with two other 3D oral mucosa models: human-sourced and porcine acellular dermal matrices (AlloDerm®/Strattice®, respectively). For the collagen matrix model, gingival fibroblasts were seeded either onto the dermal side of the AlloDerm® and Strattice® matrices or within the collagen matrices in complete culture medium (DMEM). For all scaffolds, DMEM was replaced every 24 h up to 72 h. For the full-thickness oral mucosa models, 72 h after fibroblast seeding, oral keratinocytes were seeded on the epidermal sides of AlloDerm® and Strattice® matrices or collagen matrices. All matrices and models were subjected to histological analysis, complementing phenotypic characterization by evaluation of glucose consumption, cell proliferation, gene expression and synthesis of growth factors. A higher fibroblast ratio was observed for the collagen matrix, in which the distribution of gingival fibroblasts was also more homogeneous. Metabolism, proliferation, and gene expression and synthesis of VEGF of these cells were also increased for the collagen matrix. All matrices provided a suitable substrate for oral keratinocytes adhesion, proliferation, and phenotypic expression; however, higher proliferation, stratification, and differentiation were noted when oral keratinocytes were seeded on the dermal matrices.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-11T17:36:59Z
2018-12-11T17:36:59Z
2018-09-01
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.tiv.2018.04.015
Toxicology in Vitro, v. 51, p. 34-39.
1879-3177
0887-2333
http://hdl.handle.net/11449/179844
10.1016/j.tiv.2018.04.015
2-s2.0-85046654521
2-s2.0-85046654521.pdf
url http://dx.doi.org/10.1016/j.tiv.2018.04.015
http://hdl.handle.net/11449/179844
identifier_str_mv Toxicology in Vitro, v. 51, p. 34-39.
1879-3177
0887-2333
10.1016/j.tiv.2018.04.015
2-s2.0-85046654521
2-s2.0-85046654521.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Toxicology in Vitro
0,931
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 34-39
application/pdf
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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