Hydrogel depots for local co-delivery of osteoinductive peptides and mesenchymal stem cells

Detalhes bibliográficos
Autor(a) principal: Raquel R Maia
Data de Publicação: 2014
Outros Autores: Mariana Barbosa, David B Gomes, Nuno Vale, Paula Gomes, Pedro L Granja, Cristina C Barrias
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/10216/82079
Resumo: The outcome of cell-based therapies can benefit from carefully designed cell carriers. A multifunctional injectable vehicle for the co-delivery of human mesenchymal stem cells (hMSCs) and osteoinductive peptides is proposed, to specifically direct hMSCs osteogenic differentiation. The osteogenic growth peptide (OGP) inspired the design of two peptides, where the bioactive portion of OGP was flanked by a protease-sensitive linker, or its scrambled sequence, to provide faster and slower release rates, respectively. Peptides were fully characterized and chemically grafted to alginate. Both OGP analogs released bioactive fragments in vitro, at different kinetics, which stimulated hMSCs proliferation and osteogenesis. hMSCs-laden OGP-alginate hydrogels were tested at an ectopic site in a xenograft mouse model. After 4 weeks, OGP-alginate hydrogels were more degraded and colonized by vascularized connective tissue than the control (without OGP). hMSCs were able to proliferate, migrate outward the hydrogels, produce endogenous extracellular matrix and mineralize it. Moreover, OGP-groups stimulated hMSCs osteogenesis, as compared with the control. Overall, the ability of the proposed platform to direct the fate of transplanted hMSCs in loco was demonstrated, and OGP-releasing hydrogels emerged as a potentially useful system to promote bone regeneration.
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spelling Hydrogel depots for local co-delivery of osteoinductive peptides and mesenchymal stem cellsQuímicaChemical sciencesThe outcome of cell-based therapies can benefit from carefully designed cell carriers. A multifunctional injectable vehicle for the co-delivery of human mesenchymal stem cells (hMSCs) and osteoinductive peptides is proposed, to specifically direct hMSCs osteogenic differentiation. The osteogenic growth peptide (OGP) inspired the design of two peptides, where the bioactive portion of OGP was flanked by a protease-sensitive linker, or its scrambled sequence, to provide faster and slower release rates, respectively. Peptides were fully characterized and chemically grafted to alginate. Both OGP analogs released bioactive fragments in vitro, at different kinetics, which stimulated hMSCs proliferation and osteogenesis. hMSCs-laden OGP-alginate hydrogels were tested at an ectopic site in a xenograft mouse model. After 4 weeks, OGP-alginate hydrogels were more degraded and colonized by vascularized connective tissue than the control (without OGP). hMSCs were able to proliferate, migrate outward the hydrogels, produce endogenous extracellular matrix and mineralize it. Moreover, OGP-groups stimulated hMSCs osteogenesis, as compared with the control. Overall, the ability of the proposed platform to direct the fate of transplanted hMSCs in loco was demonstrated, and OGP-releasing hydrogels emerged as a potentially useful system to promote bone regeneration.20142014-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10216/82079eng0168-365910.1016/j.jconrel.2014.06.030Raquel R MaiaMariana BarbosaDavid B GomesNuno ValePaula GomesPedro L GranjaCristina C Barriasinfo: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:RCAAP2023-11-29T13:11:41Zoai:repositorio-aberto.up.pt:10216/82079Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T23:35:34.675051Repositório 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 Hydrogel depots for local co-delivery of osteoinductive peptides and mesenchymal stem cells
title Hydrogel depots for local co-delivery of osteoinductive peptides and mesenchymal stem cells
spellingShingle Hydrogel depots for local co-delivery of osteoinductive peptides and mesenchymal stem cells
Raquel R Maia
Química
Chemical sciences
title_short Hydrogel depots for local co-delivery of osteoinductive peptides and mesenchymal stem cells
title_full Hydrogel depots for local co-delivery of osteoinductive peptides and mesenchymal stem cells
title_fullStr Hydrogel depots for local co-delivery of osteoinductive peptides and mesenchymal stem cells
title_full_unstemmed Hydrogel depots for local co-delivery of osteoinductive peptides and mesenchymal stem cells
title_sort Hydrogel depots for local co-delivery of osteoinductive peptides and mesenchymal stem cells
author Raquel R Maia
author_facet Raquel R Maia
Mariana Barbosa
David B Gomes
Nuno Vale
Paula Gomes
Pedro L Granja
Cristina C Barrias
author_role author
author2 Mariana Barbosa
David B Gomes
Nuno Vale
Paula Gomes
Pedro L Granja
Cristina C Barrias
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Raquel R Maia
Mariana Barbosa
David B Gomes
Nuno Vale
Paula Gomes
Pedro L Granja
Cristina C Barrias
dc.subject.por.fl_str_mv Química
Chemical sciences
topic Química
Chemical sciences
description The outcome of cell-based therapies can benefit from carefully designed cell carriers. A multifunctional injectable vehicle for the co-delivery of human mesenchymal stem cells (hMSCs) and osteoinductive peptides is proposed, to specifically direct hMSCs osteogenic differentiation. The osteogenic growth peptide (OGP) inspired the design of two peptides, where the bioactive portion of OGP was flanked by a protease-sensitive linker, or its scrambled sequence, to provide faster and slower release rates, respectively. Peptides were fully characterized and chemically grafted to alginate. Both OGP analogs released bioactive fragments in vitro, at different kinetics, which stimulated hMSCs proliferation and osteogenesis. hMSCs-laden OGP-alginate hydrogels were tested at an ectopic site in a xenograft mouse model. After 4 weeks, OGP-alginate hydrogels were more degraded and colonized by vascularized connective tissue than the control (without OGP). hMSCs were able to proliferate, migrate outward the hydrogels, produce endogenous extracellular matrix and mineralize it. Moreover, OGP-groups stimulated hMSCs osteogenesis, as compared with the control. Overall, the ability of the proposed platform to direct the fate of transplanted hMSCs in loco was demonstrated, and OGP-releasing hydrogels emerged as a potentially useful system to promote bone regeneration.
publishDate 2014
dc.date.none.fl_str_mv 2014
2014-01-01T00:00:00Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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status_str publishedVersion
dc.identifier.uri.fl_str_mv https://hdl.handle.net/10216/82079
url https://hdl.handle.net/10216/82079
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0168-3659
10.1016/j.jconrel.2014.06.030
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