Antimicrobial peptide-gold nanoscale therapeutic formulation with high skin regenerative potential

Detalhes bibliográficos
Autor(a) principal: Comune, Michela
Data de Publicação: 2017
Outros Autores: Rai, Akhilesh, Chereddy, Kiran K, Pinto, Sandra, Aday, Sezin, Ferreira, André F, Zonari, Alessandra, Blersch, Josephine, Cunha, Rodrigo Pinto Antunes da, Rodrigues, Ricardo, Lerma, Juan, Simões, Pedro Nuno, Préat, Veronique, Ferreira, Lino
Tipo de documento: Artigo
Idioma: por
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/92387
https://doi.org/10.1016/j.jconrel.2017.07.007
Resumo: Chronic skin wounds affect ≈3% of persons aged >60years (Davies et al., 2007) [1]. These wounds are typically difficult to heal by conventional therapies and in many cases they get infected making even harder the regeneration process. The antimicrobial peptide (AMP) LL37 combines antimicrobial with pro-regenerative properties and thus represents a promising topical therapy to address both problems. Here, we investigated the wound healing potential of soluble and immobilized LL37 (LL37-conjugated gold nanoparticles, LL37-Au NPs), both in vitro (migration of keratinocytes) and in vivo (skin wound healing). Our results show that LL37-Au NPs, but not LL37 peptide, have the capacity to prolong the phosphorylation of EGFR and ERK1/2 and enhance the migratory properties of keratinocytes in a large in vitro wound model. We further report that both LL37 and LL37-Au NPs promote keratinocyte migration by the transactivation of EGFR, a process that seems to be initiated at the P2X7 receptor, as confirmed by chemical and genetic inhibition studies. Finally, we show in vivo that LL37-Au NPs have higher wound healing activity than LL37 peptide in a splinted mouse full thickness excisional model. Animal wounds treated by LL37-Au NPs have higher expression of collagen, IL6 and VEGF than the ones treated with LL37 peptide or NPs without LL37. Altogether, the conjugation of AMPs to NPs offers a promising platform to enhance their pro-regenerative properties.
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spelling Antimicrobial peptide-gold nanoscale therapeutic formulation with high skin regenerative potentialAntimicrobial peptide; EGFR transactivation; Keratinocytes; LL37; P2X7 receptor; Purinergic receptors; Wound healingAnimalsAntimicrobial Cationic PeptidesCathelicidinsCell LineFemaleGoldHumansMetal NanoparticlesMiceRegenerationWound HealingSkin Physiological PhenomenaChronic skin wounds affect ≈3% of persons aged >60years (Davies et al., 2007) [1]. These wounds are typically difficult to heal by conventional therapies and in many cases they get infected making even harder the regeneration process. The antimicrobial peptide (AMP) LL37 combines antimicrobial with pro-regenerative properties and thus represents a promising topical therapy to address both problems. Here, we investigated the wound healing potential of soluble and immobilized LL37 (LL37-conjugated gold nanoparticles, LL37-Au NPs), both in vitro (migration of keratinocytes) and in vivo (skin wound healing). Our results show that LL37-Au NPs, but not LL37 peptide, have the capacity to prolong the phosphorylation of EGFR and ERK1/2 and enhance the migratory properties of keratinocytes in a large in vitro wound model. We further report that both LL37 and LL37-Au NPs promote keratinocyte migration by the transactivation of EGFR, a process that seems to be initiated at the P2X7 receptor, as confirmed by chemical and genetic inhibition studies. Finally, we show in vivo that LL37-Au NPs have higher wound healing activity than LL37 peptide in a splinted mouse full thickness excisional model. Animal wounds treated by LL37-Au NPs have higher expression of collagen, IL6 and VEGF than the ones treated with LL37 peptide or NPs without LL37. Altogether, the conjugation of AMPs to NPs offers a promising platform to enhance their pro-regenerative properties.The authors would like to thank the financial support of EC (ERC project nº 307384, “Nanotrigger”; Marie Curie ITN “NANODRUG”, FP7-PEOPLE-2011-ITN). The work was also funded by COMPETE in the context of the project “Stem cell based platforms for Regenerative and Therapeutic Medicine” (Centro-07-ST24-FEDER-002008).Elsevier2017-09-28info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/92387http://hdl.handle.net/10316/92387https://doi.org/10.1016/j.jconrel.2017.07.007por01683659Comune, MichelaRai, AkhileshChereddy, Kiran KPinto, SandraAday, SezinFerreira, André FZonari, AlessandraBlersch, JosephineCunha, Rodrigo Pinto Antunes daRodrigues, RicardoLerma, JuanSimões, Pedro NunoPréat, VeroniqueFerreira, Linoinfo: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:RCAAP2023-04-06T10:20:27Zoai:estudogeral.uc.pt:10316/92387Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:11:29.680410Repositório 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 Antimicrobial peptide-gold nanoscale therapeutic formulation with high skin regenerative potential
title Antimicrobial peptide-gold nanoscale therapeutic formulation with high skin regenerative potential
spellingShingle Antimicrobial peptide-gold nanoscale therapeutic formulation with high skin regenerative potential
Comune, Michela
Antimicrobial peptide; EGFR transactivation; Keratinocytes; LL37; P2X7 receptor; Purinergic receptors; Wound healing
Animals
Antimicrobial Cationic Peptides
Cathelicidins
Cell Line
Female
Gold
Humans
Metal Nanoparticles
Mice
Regeneration
Wound Healing
Skin Physiological Phenomena
title_short Antimicrobial peptide-gold nanoscale therapeutic formulation with high skin regenerative potential
title_full Antimicrobial peptide-gold nanoscale therapeutic formulation with high skin regenerative potential
title_fullStr Antimicrobial peptide-gold nanoscale therapeutic formulation with high skin regenerative potential
title_full_unstemmed Antimicrobial peptide-gold nanoscale therapeutic formulation with high skin regenerative potential
title_sort Antimicrobial peptide-gold nanoscale therapeutic formulation with high skin regenerative potential
author Comune, Michela
author_facet Comune, Michela
Rai, Akhilesh
Chereddy, Kiran K
Pinto, Sandra
Aday, Sezin
Ferreira, André F
Zonari, Alessandra
Blersch, Josephine
Cunha, Rodrigo Pinto Antunes da
Rodrigues, Ricardo
Lerma, Juan
Simões, Pedro Nuno
Préat, Veronique
Ferreira, Lino
author_role author
author2 Rai, Akhilesh
Chereddy, Kiran K
Pinto, Sandra
Aday, Sezin
Ferreira, André F
Zonari, Alessandra
Blersch, Josephine
Cunha, Rodrigo Pinto Antunes da
Rodrigues, Ricardo
Lerma, Juan
Simões, Pedro Nuno
Préat, Veronique
Ferreira, Lino
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Comune, Michela
Rai, Akhilesh
Chereddy, Kiran K
Pinto, Sandra
Aday, Sezin
Ferreira, André F
Zonari, Alessandra
Blersch, Josephine
Cunha, Rodrigo Pinto Antunes da
Rodrigues, Ricardo
Lerma, Juan
Simões, Pedro Nuno
Préat, Veronique
Ferreira, Lino
dc.subject.por.fl_str_mv Antimicrobial peptide; EGFR transactivation; Keratinocytes; LL37; P2X7 receptor; Purinergic receptors; Wound healing
Animals
Antimicrobial Cationic Peptides
Cathelicidins
Cell Line
Female
Gold
Humans
Metal Nanoparticles
Mice
Regeneration
Wound Healing
Skin Physiological Phenomena
topic Antimicrobial peptide; EGFR transactivation; Keratinocytes; LL37; P2X7 receptor; Purinergic receptors; Wound healing
Animals
Antimicrobial Cationic Peptides
Cathelicidins
Cell Line
Female
Gold
Humans
Metal Nanoparticles
Mice
Regeneration
Wound Healing
Skin Physiological Phenomena
description Chronic skin wounds affect ≈3% of persons aged >60years (Davies et al., 2007) [1]. These wounds are typically difficult to heal by conventional therapies and in many cases they get infected making even harder the regeneration process. The antimicrobial peptide (AMP) LL37 combines antimicrobial with pro-regenerative properties and thus represents a promising topical therapy to address both problems. Here, we investigated the wound healing potential of soluble and immobilized LL37 (LL37-conjugated gold nanoparticles, LL37-Au NPs), both in vitro (migration of keratinocytes) and in vivo (skin wound healing). Our results show that LL37-Au NPs, but not LL37 peptide, have the capacity to prolong the phosphorylation of EGFR and ERK1/2 and enhance the migratory properties of keratinocytes in a large in vitro wound model. We further report that both LL37 and LL37-Au NPs promote keratinocyte migration by the transactivation of EGFR, a process that seems to be initiated at the P2X7 receptor, as confirmed by chemical and genetic inhibition studies. Finally, we show in vivo that LL37-Au NPs have higher wound healing activity than LL37 peptide in a splinted mouse full thickness excisional model. Animal wounds treated by LL37-Au NPs have higher expression of collagen, IL6 and VEGF than the ones treated with LL37 peptide or NPs without LL37. Altogether, the conjugation of AMPs to NPs offers a promising platform to enhance their pro-regenerative properties.
publishDate 2017
dc.date.none.fl_str_mv 2017-09-28
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/10316/92387
http://hdl.handle.net/10316/92387
https://doi.org/10.1016/j.jconrel.2017.07.007
url http://hdl.handle.net/10316/92387
https://doi.org/10.1016/j.jconrel.2017.07.007
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv 01683659
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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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)
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