Aligned silk-based 3-D architectures for contact guidance in tissue engineering

Detalhes bibliográficos
Autor(a) principal: Oliveira, A. L.
Data de Publicação: 2012
Outros Autores: Sun, L., Kim, H. J., Rice, W., Kluge, J., Reis, R. L., Kaplan, David
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/1822/23652
Resumo: An important challenge in the biomaterials field is to mimic the structure of functional tissues via cell and extracellular matrix (ECM) alignment and anisotropy. Toward this goal, silk-based scaffolds resembling bone lamellar structure were developed using a freeze-drying technique. The structure could be controlled directly by solute concentration and freezing parameters, resulting in lamellar scaffolds with regular morphology. Different post-treatments, such as methanol, water annealing and steam sterilization, were investigated to induce water stability. The resulting structures exhibited significant differences in terms of morphological integrity, structure and mechanical properties. The lamellar thicknesses were ∼2.6 μm for the methanol-treated scaffolds and ∼5.8 μm for water-annealed. These values are in the range of those reported for human lamellar bone. Human bone marrow-derived mesenchymal stem cells (hMSC) were seeded on these silk fibroin lamellar scaffolds and grown under osteogenic conditions to assess the effect of the microstructure on cell behavior. Collagen in the newly deposited ECM was found aligned along the lamellar architectures. In the case of methanol-treated lamellar structures, the hMSC were able to migrate into the interior of the scaffolds, producing a multilamellar hybrid construct. The present morphology constitutes a useful pattern onto which hMSC cells attach and proliferate for guided formation of a highly oriented extracellular matrix.
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spelling Aligned silk-based 3-D architectures for contact guidance in tissue engineeringFreeze-dryingLamellar morphology cell alignmentSilk scaffoldTissue engineeringScience & TechnologyAn important challenge in the biomaterials field is to mimic the structure of functional tissues via cell and extracellular matrix (ECM) alignment and anisotropy. Toward this goal, silk-based scaffolds resembling bone lamellar structure were developed using a freeze-drying technique. The structure could be controlled directly by solute concentration and freezing parameters, resulting in lamellar scaffolds with regular morphology. Different post-treatments, such as methanol, water annealing and steam sterilization, were investigated to induce water stability. The resulting structures exhibited significant differences in terms of morphological integrity, structure and mechanical properties. The lamellar thicknesses were ∼2.6 μm for the methanol-treated scaffolds and ∼5.8 μm for water-annealed. These values are in the range of those reported for human lamellar bone. Human bone marrow-derived mesenchymal stem cells (hMSC) were seeded on these silk fibroin lamellar scaffolds and grown under osteogenic conditions to assess the effect of the microstructure on cell behavior. Collagen in the newly deposited ECM was found aligned along the lamellar architectures. In the case of methanol-treated lamellar structures, the hMSC were able to migrate into the interior of the scaffolds, producing a multilamellar hybrid construct. The present morphology constitutes a useful pattern onto which hMSC cells attach and proliferate for guided formation of a highly oriented extracellular matrix.A.L.O. wishes to thank financial support from the Portuguese Foundation for Science and Technology (SFRH/BPD/39102/2007) under POCTI Program. This work was partially supported by FCT through POCTI and/or FEDER programs and by the NIH [DE017207, EB003210 and EB002520].ElsevierUniversidade do MinhoOliveira, A. L.Sun, L.Kim, H. J.Rice, W.Kluge, J.Reis, R. L.Kaplan, David2012-032012-03-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/1822/23652eng1742-706110.1016/j.actbio.2011.12.01522202909http://www.sciencedirect.com/science/article/pii/S1742706111005514info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-21T12:09:07Zoai:repositorium.sdum.uminho.pt:1822/23652Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:00:28.316592Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Aligned silk-based 3-D architectures for contact guidance in tissue engineering
title Aligned silk-based 3-D architectures for contact guidance in tissue engineering
spellingShingle Aligned silk-based 3-D architectures for contact guidance in tissue engineering
Oliveira, A. L.
Freeze-drying
Lamellar morphology cell alignment
Silk scaffold
Tissue engineering
Science & Technology
title_short Aligned silk-based 3-D architectures for contact guidance in tissue engineering
title_full Aligned silk-based 3-D architectures for contact guidance in tissue engineering
title_fullStr Aligned silk-based 3-D architectures for contact guidance in tissue engineering
title_full_unstemmed Aligned silk-based 3-D architectures for contact guidance in tissue engineering
title_sort Aligned silk-based 3-D architectures for contact guidance in tissue engineering
author Oliveira, A. L.
author_facet Oliveira, A. L.
Sun, L.
Kim, H. J.
Rice, W.
Kluge, J.
Reis, R. L.
Kaplan, David
author_role author
author2 Sun, L.
Kim, H. J.
Rice, W.
Kluge, J.
Reis, R. L.
Kaplan, David
author2_role author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Oliveira, A. L.
Sun, L.
Kim, H. J.
Rice, W.
Kluge, J.
Reis, R. L.
Kaplan, David
dc.subject.por.fl_str_mv Freeze-drying
Lamellar morphology cell alignment
Silk scaffold
Tissue engineering
Science & Technology
topic Freeze-drying
Lamellar morphology cell alignment
Silk scaffold
Tissue engineering
Science & Technology
description An important challenge in the biomaterials field is to mimic the structure of functional tissues via cell and extracellular matrix (ECM) alignment and anisotropy. Toward this goal, silk-based scaffolds resembling bone lamellar structure were developed using a freeze-drying technique. The structure could be controlled directly by solute concentration and freezing parameters, resulting in lamellar scaffolds with regular morphology. Different post-treatments, such as methanol, water annealing and steam sterilization, were investigated to induce water stability. The resulting structures exhibited significant differences in terms of morphological integrity, structure and mechanical properties. The lamellar thicknesses were ∼2.6 μm for the methanol-treated scaffolds and ∼5.8 μm for water-annealed. These values are in the range of those reported for human lamellar bone. Human bone marrow-derived mesenchymal stem cells (hMSC) were seeded on these silk fibroin lamellar scaffolds and grown under osteogenic conditions to assess the effect of the microstructure on cell behavior. Collagen in the newly deposited ECM was found aligned along the lamellar architectures. In the case of methanol-treated lamellar structures, the hMSC were able to migrate into the interior of the scaffolds, producing a multilamellar hybrid construct. The present morphology constitutes a useful pattern onto which hMSC cells attach and proliferate for guided formation of a highly oriented extracellular matrix.
publishDate 2012
dc.date.none.fl_str_mv 2012-03
2012-03-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/1822/23652
url http://hdl.handle.net/1822/23652
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1742-7061
10.1016/j.actbio.2011.12.015
22202909
http://www.sciencedirect.com/science/article/pii/S1742706111005514
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dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
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