BDNF gene delivery mediated by neuron-targeted nanoparticles is neuroprotective in peripheral nerve injury

Detalhes bibliográficos
Autor(a) principal: Lopes, CDF
Data de Publicação: 2017
Outros Autores: Gonçalves, NP, Gomes, CP, Saraiva, MJ, Pêgo, AP
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10216/110343
Resumo: Neuron-targeted gene delivery is a promising strategy to treat peripheral neuropathies. Here we propose the use of polymeric nanoparticles based on thiolated trimethyl chitosan (TMCSH) to mediate targeted gene delivery to peripheral neurons upon a peripheral and minimally invasive intramuscular administration. Nanoparticles were grafted with the non-toxic carboxylic fragment of the tetanus neurotoxin (HC) to allow neuron targeting and were explored to deliver a plasmid DNA encoding for the brain-derived neurotrophic factor (BDNF) in a peripheral nerve injury model. The TMCSH-HC/BDNF nanoparticle treatment promoted the release and significant expression of BDNF in neural tissues, which resulted in an enhanced functional recovery after injury as compared to control treatments (vehicle and non-targeted nanoparticles), associated with an improvement in key pro-regenerative events, namely, the increased expression of neurofilament and growth-associated protein GAP-43 in the injured nerves. Moreover, the targeted nanoparticle treatment was correlated with a significantly higher density of myelinated axons in the distal stump of injured nerves, as well as with preservation of unmyelinated axon density as compared with controls and a protective role in injury-denervated muscles, preventing them from denervation. These results highlight the potential of TMCSH-HC nanoparticles as non-viral gene carriers to deliver therapeutic genes into the peripheral neurons and thus, pave the way for their use as an effective therapeutic intervention for peripheral neuropathies.
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spelling BDNF gene delivery mediated by neuron-targeted nanoparticles is neuroprotective in peripheral nerve injuryAnimalsBrain-Derived Neurotrophic Factor/geneticsFemaleGenetic Therapy/methodsMiceMice Inbred BALB CNanocapsules/administration & dosageNanocapsules/chemistryNeurons/chemistryPeripheral Nerve Injuries/geneticsPeripheral Nerve Injuries/pathologyPeripheral Nerve Injuries/therapyPlasmids/administration & dosagePlasmids/geneticsTreatment OutcomeNeuron-targeted gene delivery is a promising strategy to treat peripheral neuropathies. Here we propose the use of polymeric nanoparticles based on thiolated trimethyl chitosan (TMCSH) to mediate targeted gene delivery to peripheral neurons upon a peripheral and minimally invasive intramuscular administration. Nanoparticles were grafted with the non-toxic carboxylic fragment of the tetanus neurotoxin (HC) to allow neuron targeting and were explored to deliver a plasmid DNA encoding for the brain-derived neurotrophic factor (BDNF) in a peripheral nerve injury model. The TMCSH-HC/BDNF nanoparticle treatment promoted the release and significant expression of BDNF in neural tissues, which resulted in an enhanced functional recovery after injury as compared to control treatments (vehicle and non-targeted nanoparticles), associated with an improvement in key pro-regenerative events, namely, the increased expression of neurofilament and growth-associated protein GAP-43 in the injured nerves. Moreover, the targeted nanoparticle treatment was correlated with a significantly higher density of myelinated axons in the distal stump of injured nerves, as well as with preservation of unmyelinated axon density as compared with controls and a protective role in injury-denervated muscles, preventing them from denervation. These results highlight the potential of TMCSH-HC nanoparticles as non-viral gene carriers to deliver therapeutic genes into the peripheral neurons and thus, pave the way for their use as an effective therapeutic intervention for peripheral neuropathies.Elsevier20172017-01-01T00:00:00Z2019-03-31T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfapplication/pdfhttp://hdl.handle.net/10216/110343eng0142-961210.1016/j.biomaterials.2016.12.025Lopes, CDFGonçalves, NPGomes, CPSaraiva, MJPêgo, APinfo:eu-repo/semantics/embargoedAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-11-29T13:59:49Zoai:repositorio-aberto.up.pt:10216/110343Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T23:51:56.090265Repositório 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 BDNF gene delivery mediated by neuron-targeted nanoparticles is neuroprotective in peripheral nerve injury
title BDNF gene delivery mediated by neuron-targeted nanoparticles is neuroprotective in peripheral nerve injury
spellingShingle BDNF gene delivery mediated by neuron-targeted nanoparticles is neuroprotective in peripheral nerve injury
Lopes, CDF
Animals
Brain-Derived Neurotrophic Factor/genetics
Female
Genetic Therapy/methods
Mice
Mice Inbred BALB C
Nanocapsules/administration & dosage
Nanocapsules/chemistry
Neurons/chemistry
Peripheral Nerve Injuries/genetics
Peripheral Nerve Injuries/pathology
Peripheral Nerve Injuries/therapy
Plasmids/administration & dosage
Plasmids/genetics
Treatment Outcome
title_short BDNF gene delivery mediated by neuron-targeted nanoparticles is neuroprotective in peripheral nerve injury
title_full BDNF gene delivery mediated by neuron-targeted nanoparticles is neuroprotective in peripheral nerve injury
title_fullStr BDNF gene delivery mediated by neuron-targeted nanoparticles is neuroprotective in peripheral nerve injury
title_full_unstemmed BDNF gene delivery mediated by neuron-targeted nanoparticles is neuroprotective in peripheral nerve injury
title_sort BDNF gene delivery mediated by neuron-targeted nanoparticles is neuroprotective in peripheral nerve injury
author Lopes, CDF
author_facet Lopes, CDF
Gonçalves, NP
Gomes, CP
Saraiva, MJ
Pêgo, AP
author_role author
author2 Gonçalves, NP
Gomes, CP
Saraiva, MJ
Pêgo, AP
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Lopes, CDF
Gonçalves, NP
Gomes, CP
Saraiva, MJ
Pêgo, AP
dc.subject.por.fl_str_mv Animals
Brain-Derived Neurotrophic Factor/genetics
Female
Genetic Therapy/methods
Mice
Mice Inbred BALB C
Nanocapsules/administration & dosage
Nanocapsules/chemistry
Neurons/chemistry
Peripheral Nerve Injuries/genetics
Peripheral Nerve Injuries/pathology
Peripheral Nerve Injuries/therapy
Plasmids/administration & dosage
Plasmids/genetics
Treatment Outcome
topic Animals
Brain-Derived Neurotrophic Factor/genetics
Female
Genetic Therapy/methods
Mice
Mice Inbred BALB C
Nanocapsules/administration & dosage
Nanocapsules/chemistry
Neurons/chemistry
Peripheral Nerve Injuries/genetics
Peripheral Nerve Injuries/pathology
Peripheral Nerve Injuries/therapy
Plasmids/administration & dosage
Plasmids/genetics
Treatment Outcome
description Neuron-targeted gene delivery is a promising strategy to treat peripheral neuropathies. Here we propose the use of polymeric nanoparticles based on thiolated trimethyl chitosan (TMCSH) to mediate targeted gene delivery to peripheral neurons upon a peripheral and minimally invasive intramuscular administration. Nanoparticles were grafted with the non-toxic carboxylic fragment of the tetanus neurotoxin (HC) to allow neuron targeting and were explored to deliver a plasmid DNA encoding for the brain-derived neurotrophic factor (BDNF) in a peripheral nerve injury model. The TMCSH-HC/BDNF nanoparticle treatment promoted the release and significant expression of BDNF in neural tissues, which resulted in an enhanced functional recovery after injury as compared to control treatments (vehicle and non-targeted nanoparticles), associated with an improvement in key pro-regenerative events, namely, the increased expression of neurofilament and growth-associated protein GAP-43 in the injured nerves. Moreover, the targeted nanoparticle treatment was correlated with a significantly higher density of myelinated axons in the distal stump of injured nerves, as well as with preservation of unmyelinated axon density as compared with controls and a protective role in injury-denervated muscles, preventing them from denervation. These results highlight the potential of TMCSH-HC nanoparticles as non-viral gene carriers to deliver therapeutic genes into the peripheral neurons and thus, pave the way for their use as an effective therapeutic intervention for peripheral neuropathies.
publishDate 2017
dc.date.none.fl_str_mv 2017
2017-01-01T00:00:00Z
2019-03-31T00:00:00Z
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 http://hdl.handle.net/10216/110343
url http://hdl.handle.net/10216/110343
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0142-9612
10.1016/j.biomaterials.2016.12.025
dc.rights.driver.fl_str_mv info:eu-repo/semantics/embargoedAccess
eu_rights_str_mv embargoedAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
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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