Poly(trimethylene carbonate-co-e-caprolactone) promotes axonal growth

Detalhes bibliográficos
Autor(a) principal: Rocha, DN
Data de Publicação: 2014
Outros Autores: Brites, P, Fonseca, C, Pêgo, AP
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/10216/120728
Resumo: Mammalian central nervous system (CNS) neurons do not regenerate after injury due to the inhibitory environment formed by the glial scar, largely constituted by myelin debris. The use of biomaterials to bridge the lesion area and the creation of an environment favoring axonal regeneration is an appealing approach, currently under investigation. This work aimed at assessing the suitability of three candidate polymers - poly(e-caprolactone), poly(trimethylene carbonate-co-e-caprolactone) (P(TMC-CL)) (11:89 mol%) and poly(trimethylene carbonate) - with the final goal of using these materials in the development of conduits to promote spinal cord regeneration. Poly(L-lysine) (PLL) coated polymeric films were tested for neuronal cell adhesion and neurite outgrowth. At similar PLL film area coverage conditions, neuronal polarization and axonal elongation was significantly higher on P(TMC-CL) films. Furthermore, cortical neurons cultured on P(TMC-CL) were able to extend neurites even when seeded onto myelin. This effect was found to be mediated by the glycogen synthase kinase 3ß (GSK3ß) signaling pathway with impact on the collapsin response mediator protein 4 (CRMP4), suggesting that besides surface topography, nanomechanical properties were implicated in this process. The obtained results indicate P(TMC-CL) as a promising material for CNS regenerativ e applications as it promotes axonal growth, overcoming myelin inhibition.
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spelling Poly(trimethylene carbonate-co-e-caprolactone) promotes axonal growthAnimalsAxons/drug effectsAxons/metabolismCell Adhesion/drug effectsCerebral Cortex/cytologyCerebral Cortex/metabolismFemaleGlycogen Synthase Kinase 3/metabolismGlycogen Synthase Kinase 3 betaMyelin Sheath/metabolismNeurites/drug effectsNeurites/metabolismNeurons/drug effectsNeurons/metabolismPolyesters/pharmacologyRatsSignal Transduction/drug effectsMammalian central nervous system (CNS) neurons do not regenerate after injury due to the inhibitory environment formed by the glial scar, largely constituted by myelin debris. The use of biomaterials to bridge the lesion area and the creation of an environment favoring axonal regeneration is an appealing approach, currently under investigation. This work aimed at assessing the suitability of three candidate polymers - poly(e-caprolactone), poly(trimethylene carbonate-co-e-caprolactone) (P(TMC-CL)) (11:89 mol%) and poly(trimethylene carbonate) - with the final goal of using these materials in the development of conduits to promote spinal cord regeneration. Poly(L-lysine) (PLL) coated polymeric films were tested for neuronal cell adhesion and neurite outgrowth. At similar PLL film area coverage conditions, neuronal polarization and axonal elongation was significantly higher on P(TMC-CL) films. Furthermore, cortical neurons cultured on P(TMC-CL) were able to extend neurites even when seeded onto myelin. This effect was found to be mediated by the glycogen synthase kinase 3ß (GSK3ß) signaling pathway with impact on the collapsin response mediator protein 4 (CRMP4), suggesting that besides surface topography, nanomechanical properties were implicated in this process. The obtained results indicate P(TMC-CL) as a promising material for CNS regenerativ e applications as it promotes axonal growth, overcoming myelin inhibition.Public Library of Science20142014-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/10216/120728eng1932-620310.1371/journal.pone.0088593Rocha, DNBrites, PFonseca, CPêgo, APinfo: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:RCAAP2023-11-29T13:59:37Zoai:repositorio-aberto.up.pt:10216/120728Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T23:51:50.891880Repositório 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 Poly(trimethylene carbonate-co-e-caprolactone) promotes axonal growth
title Poly(trimethylene carbonate-co-e-caprolactone) promotes axonal growth
spellingShingle Poly(trimethylene carbonate-co-e-caprolactone) promotes axonal growth
Rocha, DN
Animals
Axons/drug effects
Axons/metabolism
Cell Adhesion/drug effects
Cerebral Cortex/cytology
Cerebral Cortex/metabolism
Female
Glycogen Synthase Kinase 3/metabolism
Glycogen Synthase Kinase 3 beta
Myelin Sheath/metabolism
Neurites/drug effects
Neurites/metabolism
Neurons/drug effects
Neurons/metabolism
Polyesters/pharmacology
Rats
Signal Transduction/drug effects
title_short Poly(trimethylene carbonate-co-e-caprolactone) promotes axonal growth
title_full Poly(trimethylene carbonate-co-e-caprolactone) promotes axonal growth
title_fullStr Poly(trimethylene carbonate-co-e-caprolactone) promotes axonal growth
title_full_unstemmed Poly(trimethylene carbonate-co-e-caprolactone) promotes axonal growth
title_sort Poly(trimethylene carbonate-co-e-caprolactone) promotes axonal growth
author Rocha, DN
author_facet Rocha, DN
Brites, P
Fonseca, C
Pêgo, AP
author_role author
author2 Brites, P
Fonseca, C
Pêgo, AP
author2_role author
author
author
dc.contributor.author.fl_str_mv Rocha, DN
Brites, P
Fonseca, C
Pêgo, AP
dc.subject.por.fl_str_mv Animals
Axons/drug effects
Axons/metabolism
Cell Adhesion/drug effects
Cerebral Cortex/cytology
Cerebral Cortex/metabolism
Female
Glycogen Synthase Kinase 3/metabolism
Glycogen Synthase Kinase 3 beta
Myelin Sheath/metabolism
Neurites/drug effects
Neurites/metabolism
Neurons/drug effects
Neurons/metabolism
Polyesters/pharmacology
Rats
Signal Transduction/drug effects
topic Animals
Axons/drug effects
Axons/metabolism
Cell Adhesion/drug effects
Cerebral Cortex/cytology
Cerebral Cortex/metabolism
Female
Glycogen Synthase Kinase 3/metabolism
Glycogen Synthase Kinase 3 beta
Myelin Sheath/metabolism
Neurites/drug effects
Neurites/metabolism
Neurons/drug effects
Neurons/metabolism
Polyesters/pharmacology
Rats
Signal Transduction/drug effects
description Mammalian central nervous system (CNS) neurons do not regenerate after injury due to the inhibitory environment formed by the glial scar, largely constituted by myelin debris. The use of biomaterials to bridge the lesion area and the creation of an environment favoring axonal regeneration is an appealing approach, currently under investigation. This work aimed at assessing the suitability of three candidate polymers - poly(e-caprolactone), poly(trimethylene carbonate-co-e-caprolactone) (P(TMC-CL)) (11:89 mol%) and poly(trimethylene carbonate) - with the final goal of using these materials in the development of conduits to promote spinal cord regeneration. Poly(L-lysine) (PLL) coated polymeric films were tested for neuronal cell adhesion and neurite outgrowth. At similar PLL film area coverage conditions, neuronal polarization and axonal elongation was significantly higher on P(TMC-CL) films. Furthermore, cortical neurons cultured on P(TMC-CL) were able to extend neurites even when seeded onto myelin. This effect was found to be mediated by the glycogen synthase kinase 3ß (GSK3ß) signaling pathway with impact on the collapsin response mediator protein 4 (CRMP4), suggesting that besides surface topography, nanomechanical properties were implicated in this process. The obtained results indicate P(TMC-CL) as a promising material for CNS regenerativ e applications as it promotes axonal growth, overcoming myelin inhibition.
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
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv https://hdl.handle.net/10216/120728
url https://hdl.handle.net/10216/120728
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1932-6203
10.1371/journal.pone.0088593
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Public Library of Science
publisher.none.fl_str_mv Public Library of Science
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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