Improved diabetic wound healing by LFcinB is associated with relevant changes in the skin immune response and microbiota
| Autor(a) principal: | |
|---|---|
| Data de Publicação: | 2021 |
| Outros Autores: | , , , , , , , , |
| Tipo de documento: | Artigo |
| Idioma: | eng |
| Título da fonte: | Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
| Texto Completo: | https://hdl.handle.net/10316/105248 https://doi.org/10.1016/j.omtm.2021.02.008 |
Resumo: | Bovine lactoferricin (LFcinB) has antimicrobial and immunomodulatory properties; however, the effects on diabetic wound healing remain poorly understood. The wound healing potential of LFcinB was investigated with in vitro, ex vivo, and in vivo models. Cell migration and proliferation were tested on keratinocytes and on porcine ears. A type 1 diabetic mouse model was also used to evaluate wound healing kinetics, bacterial diversity patterns, and the effect of LFcinB on oxidative stress, macrophage phenotype, angiogenesis, and collagen deposition. LFcinB increased keratinocyte migration in vitro (p < 0.05) and ex vivo (p < 0.001) and improved wound healing in diabetic mice (p < 0.05), though not in normoglycemic control mice. In diabetic mouse wounds, LFcinB treatment led to the eradication of Bacillus pumilus, a decrease in Staphylococcus aureus, and an increase in the Staphylococcus xylosus prevalence. LFcinB increased angiogenesis in diabetic mice (p < 0.01), but this was decreased in control mice (p < 0.05). LFcinB improved collagen deposition in both diabetic and control mice (p < 0.05). Both oxidative stress and the M1-to-M2 macrophage ratios were decreased in LFcinB-treated wounds of diabetic animals (p < 0.001 and p < 0.05, respectively) compared with saline, suggesting a downregulation of inflammation in diabetic wounds. In conclusion, LFcinB treatment demonstrated noticeable positive effects on diabetic wound healing. |
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Improved diabetic wound healing by LFcinB is associated with relevant changes in the skin immune response and microbiotabacterial diversity; bovine lactoferricin; collagen deposition; diabetes; immunomodulation; inflammatory cytokines; macrophage polarization; wound healingBovine lactoferricin (LFcinB) has antimicrobial and immunomodulatory properties; however, the effects on diabetic wound healing remain poorly understood. The wound healing potential of LFcinB was investigated with in vitro, ex vivo, and in vivo models. Cell migration and proliferation were tested on keratinocytes and on porcine ears. A type 1 diabetic mouse model was also used to evaluate wound healing kinetics, bacterial diversity patterns, and the effect of LFcinB on oxidative stress, macrophage phenotype, angiogenesis, and collagen deposition. LFcinB increased keratinocyte migration in vitro (p < 0.05) and ex vivo (p < 0.001) and improved wound healing in diabetic mice (p < 0.05), though not in normoglycemic control mice. In diabetic mouse wounds, LFcinB treatment led to the eradication of Bacillus pumilus, a decrease in Staphylococcus aureus, and an increase in the Staphylococcus xylosus prevalence. LFcinB increased angiogenesis in diabetic mice (p < 0.01), but this was decreased in control mice (p < 0.05). LFcinB improved collagen deposition in both diabetic and control mice (p < 0.05). Both oxidative stress and the M1-to-M2 macrophage ratios were decreased in LFcinB-treated wounds of diabetic animals (p < 0.001 and p < 0.05, respectively) compared with saline, suggesting a downregulation of inflammation in diabetic wounds. In conclusion, LFcinB treatment demonstrated noticeable positive effects on diabetic wound healing.Funding for in vivo work was funded by FEDER-COMPETE-2020-UID/NEU/04539/2013, POCI01-0145-FEDER-007440, UIDB/04539/2020, Healthy Aging 2020-CENTRO-01-0145-FEDER-000012-N2323, DL57/2016/CP1448/CT0024, NIGMS P20GM109096, 5P30-AG028718, and EFSD European Research Programme in Microvascular Complications/Novartis Pharma AG. Microbial sampling and isolation procedures from animals were carried out with support from the Infarmed grant FIS-FIS2015-01_DIA_20150630-144.Elsevier2021-03-12info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://hdl.handle.net/10316/105248https://hdl.handle.net/10316/105248https://doi.org/10.1016/j.omtm.2021.02.008eng2329-0501Mouritzen, Michelle V.Petkovic, MarijaQvist, KatrinePoulsen, Steen S.Alarico, SusanaLeal, Ermelindo C.Dalgaard, Louise T.Empadinhas, NunoCarvalho, EugeniaJenssen, Håvardinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2025-01-30T12:18:01Zoai:estudogeral.uc.pt:10316/105248Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T05:55:43.866585Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse |
| dc.title.none.fl_str_mv |
Improved diabetic wound healing by LFcinB is associated with relevant changes in the skin immune response and microbiota |
| title |
Improved diabetic wound healing by LFcinB is associated with relevant changes in the skin immune response and microbiota |
| spellingShingle |
Improved diabetic wound healing by LFcinB is associated with relevant changes in the skin immune response and microbiota Mouritzen, Michelle V. bacterial diversity; bovine lactoferricin; collagen deposition; diabetes; immunomodulation; inflammatory cytokines; macrophage polarization; wound healing |
| title_short |
Improved diabetic wound healing by LFcinB is associated with relevant changes in the skin immune response and microbiota |
| title_full |
Improved diabetic wound healing by LFcinB is associated with relevant changes in the skin immune response and microbiota |
| title_fullStr |
Improved diabetic wound healing by LFcinB is associated with relevant changes in the skin immune response and microbiota |
| title_full_unstemmed |
Improved diabetic wound healing by LFcinB is associated with relevant changes in the skin immune response and microbiota |
| title_sort |
Improved diabetic wound healing by LFcinB is associated with relevant changes in the skin immune response and microbiota |
| author |
Mouritzen, Michelle V. |
| author_facet |
Mouritzen, Michelle V. Petkovic, Marija Qvist, Katrine Poulsen, Steen S. Alarico, Susana Leal, Ermelindo C. Dalgaard, Louise T. Empadinhas, Nuno Carvalho, Eugenia Jenssen, Håvard |
| author_role |
author |
| author2 |
Petkovic, Marija Qvist, Katrine Poulsen, Steen S. Alarico, Susana Leal, Ermelindo C. Dalgaard, Louise T. Empadinhas, Nuno Carvalho, Eugenia Jenssen, Håvard |
| author2_role |
author author author author author author author author author |
| dc.contributor.author.fl_str_mv |
Mouritzen, Michelle V. Petkovic, Marija Qvist, Katrine Poulsen, Steen S. Alarico, Susana Leal, Ermelindo C. Dalgaard, Louise T. Empadinhas, Nuno Carvalho, Eugenia Jenssen, Håvard |
| dc.subject.por.fl_str_mv |
bacterial diversity; bovine lactoferricin; collagen deposition; diabetes; immunomodulation; inflammatory cytokines; macrophage polarization; wound healing |
| topic |
bacterial diversity; bovine lactoferricin; collagen deposition; diabetes; immunomodulation; inflammatory cytokines; macrophage polarization; wound healing |
| description |
Bovine lactoferricin (LFcinB) has antimicrobial and immunomodulatory properties; however, the effects on diabetic wound healing remain poorly understood. The wound healing potential of LFcinB was investigated with in vitro, ex vivo, and in vivo models. Cell migration and proliferation were tested on keratinocytes and on porcine ears. A type 1 diabetic mouse model was also used to evaluate wound healing kinetics, bacterial diversity patterns, and the effect of LFcinB on oxidative stress, macrophage phenotype, angiogenesis, and collagen deposition. LFcinB increased keratinocyte migration in vitro (p < 0.05) and ex vivo (p < 0.001) and improved wound healing in diabetic mice (p < 0.05), though not in normoglycemic control mice. In diabetic mouse wounds, LFcinB treatment led to the eradication of Bacillus pumilus, a decrease in Staphylococcus aureus, and an increase in the Staphylococcus xylosus prevalence. LFcinB increased angiogenesis in diabetic mice (p < 0.01), but this was decreased in control mice (p < 0.05). LFcinB improved collagen deposition in both diabetic and control mice (p < 0.05). Both oxidative stress and the M1-to-M2 macrophage ratios were decreased in LFcinB-treated wounds of diabetic animals (p < 0.001 and p < 0.05, respectively) compared with saline, suggesting a downregulation of inflammation in diabetic wounds. In conclusion, LFcinB treatment demonstrated noticeable positive effects on diabetic wound healing. |
| publishDate |
2021 |
| dc.date.none.fl_str_mv |
2021-03-12 |
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info:eu-repo/semantics/publishedVersion |
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info:eu-repo/semantics/article |
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article |
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publishedVersion |
| dc.identifier.uri.fl_str_mv |
https://hdl.handle.net/10316/105248 https://hdl.handle.net/10316/105248 https://doi.org/10.1016/j.omtm.2021.02.008 |
| url |
https://hdl.handle.net/10316/105248 https://doi.org/10.1016/j.omtm.2021.02.008 |
| dc.language.iso.fl_str_mv |
eng |
| language |
eng |
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2329-0501 |
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info:eu-repo/semantics/openAccess |
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openAccess |
| dc.publisher.none.fl_str_mv |
Elsevier |
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Elsevier |
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Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) |
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info@rcaap.pt |
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