Phenotypic markers of oral keratinocytes seeded on two distinct 3D oral mucosa models
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , |
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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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 |
_version_ |
1813546433607892992 |