Entrapped in cage (EiC) scaffolds of 3D-printed polycaprolactone and porous silk fibroin for meniscus tissue engineering
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | https://hdl.handle.net/1822/66384 |
Resumo: | The meniscus has critical functions in the knee joint kinematics and homeostasis. Injuries of the meniscus are frequent, and the lack of a functional meniscus between the femur and tibial plateau can cause articular cartilage degeneration leading to osteoarthritis development and progression. Regeneration of meniscus tissue has outstanding challenges to be addressed. In the current study, novel Entrapped in Cage (EiC) scaffolds of 3D-printed polycaprolactone (PCL) and porous silk fibroin were proposed for meniscus tissue engineering. As confirmed by micro-structural analysis the entrapment of silk fibroin was successful, and all scaffolds had excellent interconnectivity (â ¥ 99%). The EiC scaffolds had more favorable microstructure compared with the PCL cage scaffolds by improving the pore size while keeping the interconnectivity almost the same. When compared with the PCL cage, the entrapment of porous silk fibroin into the PCL cage decreased the high compressive modulus in a favorable matter in the wet state thanks to the silk fibroinâ s high swelling properties. The in vitro studies with human stem cells or meniscocytes seeded constructs, demonstrated that the EiC scaffolds had superior cell adhesion, metabolic activity, and proliferation compared to the PCL cage scaffolds. Upon subcutaneous implantation of scaffolds in nude mice, all groups were free of adverse incidents, and mildly invaded by inflammatory cells with neovascularization, while the EiC scaffolds showed better tissue infiltration. The results of this work indicated that the EiC scaffolds of PCL and silk fibroin are favorable for meniscus tissue engineering, and the findings are encouraging for further studies using a larger animal model. |
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Entrapped in cage (EiC) scaffolds of 3D-printed polycaprolactone and porous silk fibroin for meniscus tissue engineeringMeniscusScaffoldSilk fibroinPolycaprolactoneMeniscocytesHuman adipose-derived stem cellsTissue engineeringScience & TechnologyThe meniscus has critical functions in the knee joint kinematics and homeostasis. Injuries of the meniscus are frequent, and the lack of a functional meniscus between the femur and tibial plateau can cause articular cartilage degeneration leading to osteoarthritis development and progression. Regeneration of meniscus tissue has outstanding challenges to be addressed. In the current study, novel Entrapped in Cage (EiC) scaffolds of 3D-printed polycaprolactone (PCL) and porous silk fibroin were proposed for meniscus tissue engineering. As confirmed by micro-structural analysis the entrapment of silk fibroin was successful, and all scaffolds had excellent interconnectivity (â ¥ 99%). The EiC scaffolds had more favorable microstructure compared with the PCL cage scaffolds by improving the pore size while keeping the interconnectivity almost the same. When compared with the PCL cage, the entrapment of porous silk fibroin into the PCL cage decreased the high compressive modulus in a favorable matter in the wet state thanks to the silk fibroinâ s high swelling properties. The in vitro studies with human stem cells or meniscocytes seeded constructs, demonstrated that the EiC scaffolds had superior cell adhesion, metabolic activity, and proliferation compared to the PCL cage scaffolds. Upon subcutaneous implantation of scaffolds in nude mice, all groups were free of adverse incidents, and mildly invaded by inflammatory cells with neovascularization, while the EiC scaffolds showed better tissue infiltration. The results of this work indicated that the EiC scaffolds of PCL and silk fibroin are favorable for meniscus tissue engineering, and the findings are encouraging for further studies using a larger animal model.This article is a result of the project FROnTHERA (NORTE-01-0145-FEDER-000023), supported by Norte Portugal Regional Operational Programme (NORTE 2020), under the PORTUGAL 2020 Partnership Agreement, through the European Regional Development Fund (ERDF). This study was also supported by the FP7 Marie Curie Initial Training Network "MultiScaleHuman: Multi-scale Biological Modalities for Physiological Human Articulation" (Contract number MRTN-CT-2011-289897). I. F. Cengiz thanks the Portuguese Foundation for Science and Technology (FCT) for the Ph.D. scholarship (SFRH/BD/99555/2014). J. M. Oliveira also thanks the FCT for the funds provided under the program Investigador FCT 2015 (IF/01285/2015). The authors thank Dr. Isabel B. Leonor and Ms. Teresa Oliveira for technical support. The funding sources had no role in the study design, the data collection, analysis, interpretation, or the preparation and submission of this work for publicationIOP PublishingUniversidade do MinhoCengiz, I. F.Maia, F. Raquelda Silva Morais, AlainSilva-Correia, JoanaPereira, H.Canadas, Raphael FaustinoEspregueira-Mendes, JoãoKwon, Il KeunReis, R. L.Oliveira, Joaquim M.20202020-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/1822/66384engCengiz I. F., Maia F. R., Morais A., Silva-Correia J., Pereira H., Canadas R. F., Espregueira-Mendes J., Kwon I. K., Reis R. M., Oliveira J. M. Entrapped in Cage (EiC) Scaffolds of 3D-Printed Polycaprolactone and Porous Silk Fibroin for Meniscus Tissue Engineering, Biofabrication, doi:10.1088/1758-5090/ab779f, 20201758-50821758-509010.1088/1758-5090/ab779f32069441https://iopscience.iop.org/article/10.1088/1758-5090/ab779finfo: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:RCAAP2023-10-07T01:21:04Zoai:repositorium.sdum.uminho.pt:1822/66384Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:14:30.626944Repositório 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 |
Entrapped in cage (EiC) scaffolds of 3D-printed polycaprolactone and porous silk fibroin for meniscus tissue engineering |
title |
Entrapped in cage (EiC) scaffolds of 3D-printed polycaprolactone and porous silk fibroin for meniscus tissue engineering |
spellingShingle |
Entrapped in cage (EiC) scaffolds of 3D-printed polycaprolactone and porous silk fibroin for meniscus tissue engineering Cengiz, I. F. Meniscus Scaffold Silk fibroin Polycaprolactone Meniscocytes Human adipose-derived stem cells Tissue engineering Science & Technology |
title_short |
Entrapped in cage (EiC) scaffolds of 3D-printed polycaprolactone and porous silk fibroin for meniscus tissue engineering |
title_full |
Entrapped in cage (EiC) scaffolds of 3D-printed polycaprolactone and porous silk fibroin for meniscus tissue engineering |
title_fullStr |
Entrapped in cage (EiC) scaffolds of 3D-printed polycaprolactone and porous silk fibroin for meniscus tissue engineering |
title_full_unstemmed |
Entrapped in cage (EiC) scaffolds of 3D-printed polycaprolactone and porous silk fibroin for meniscus tissue engineering |
title_sort |
Entrapped in cage (EiC) scaffolds of 3D-printed polycaprolactone and porous silk fibroin for meniscus tissue engineering |
author |
Cengiz, I. F. |
author_facet |
Cengiz, I. F. Maia, F. Raquel da Silva Morais, Alain Silva-Correia, Joana Pereira, H. Canadas, Raphael Faustino Espregueira-Mendes, João Kwon, Il Keun Reis, R. L. Oliveira, Joaquim M. |
author_role |
author |
author2 |
Maia, F. Raquel da Silva Morais, Alain Silva-Correia, Joana Pereira, H. Canadas, Raphael Faustino Espregueira-Mendes, João Kwon, Il Keun Reis, R. L. Oliveira, Joaquim M. |
author2_role |
author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Universidade do Minho |
dc.contributor.author.fl_str_mv |
Cengiz, I. F. Maia, F. Raquel da Silva Morais, Alain Silva-Correia, Joana Pereira, H. Canadas, Raphael Faustino Espregueira-Mendes, João Kwon, Il Keun Reis, R. L. Oliveira, Joaquim M. |
dc.subject.por.fl_str_mv |
Meniscus Scaffold Silk fibroin Polycaprolactone Meniscocytes Human adipose-derived stem cells Tissue engineering Science & Technology |
topic |
Meniscus Scaffold Silk fibroin Polycaprolactone Meniscocytes Human adipose-derived stem cells Tissue engineering Science & Technology |
description |
The meniscus has critical functions in the knee joint kinematics and homeostasis. Injuries of the meniscus are frequent, and the lack of a functional meniscus between the femur and tibial plateau can cause articular cartilage degeneration leading to osteoarthritis development and progression. Regeneration of meniscus tissue has outstanding challenges to be addressed. In the current study, novel Entrapped in Cage (EiC) scaffolds of 3D-printed polycaprolactone (PCL) and porous silk fibroin were proposed for meniscus tissue engineering. As confirmed by micro-structural analysis the entrapment of silk fibroin was successful, and all scaffolds had excellent interconnectivity (â ¥ 99%). The EiC scaffolds had more favorable microstructure compared with the PCL cage scaffolds by improving the pore size while keeping the interconnectivity almost the same. When compared with the PCL cage, the entrapment of porous silk fibroin into the PCL cage decreased the high compressive modulus in a favorable matter in the wet state thanks to the silk fibroinâ s high swelling properties. The in vitro studies with human stem cells or meniscocytes seeded constructs, demonstrated that the EiC scaffolds had superior cell adhesion, metabolic activity, and proliferation compared to the PCL cage scaffolds. Upon subcutaneous implantation of scaffolds in nude mice, all groups were free of adverse incidents, and mildly invaded by inflammatory cells with neovascularization, while the EiC scaffolds showed better tissue infiltration. The results of this work indicated that the EiC scaffolds of PCL and silk fibroin are favorable for meniscus tissue engineering, and the findings are encouraging for further studies using a larger animal model. |
publishDate |
2020 |
dc.date.none.fl_str_mv |
2020 2020-01-01T00:00:00Z |
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 |
https://hdl.handle.net/1822/66384 |
url |
https://hdl.handle.net/1822/66384 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Cengiz I. F., Maia F. R., Morais A., Silva-Correia J., Pereira H., Canadas R. F., Espregueira-Mendes J., Kwon I. K., Reis R. M., Oliveira J. M. Entrapped in Cage (EiC) Scaffolds of 3D-Printed Polycaprolactone and Porous Silk Fibroin for Meniscus Tissue Engineering, Biofabrication, doi:10.1088/1758-5090/ab779f, 2020 1758-5082 1758-5090 10.1088/1758-5090/ab779f 32069441 https://iopscience.iop.org/article/10.1088/1758-5090/ab779f |
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info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
IOP Publishing |
publisher.none.fl_str_mv |
IOP Publishing |
dc.source.none.fl_str_mv |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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