Antimicrobial peptide-gold nanoscale therapeutic formulation with high skin regenerative potential
Autor(a) principal: | |
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Data de Publicação: | 2017 |
Outros Autores: | , , , , , , , , , , , , |
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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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 |
eu_rights_str_mv |
openAccess |
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 |
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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 |
repository.mail.fl_str_mv |
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1799134012038447104 |