Controlling Macrophage Polarization to Modulate Inflammatory Cues Using Immune-Switch Nanoparticles

Detalhes bibliográficos
Autor(a) principal: Almeida, A. F.
Data de Publicação: 2022
Outros Autores: Miranda, M. S., Vinhas, Carla Adriana Araújo, Gonçalves, A I, Gomes, Manuela E., Rodrigues, Márcia T.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: https://hdl.handle.net/1822/81138
Resumo: The persistence of inflammatory mediators in tissue niches significantly impacts regenerative outcomes and contributes to chronic diseases. Interleukin-4 (IL4) boosts pro-healing phenotypes in macrophages (MÏ ) and triggers the activation of signal transducer and activator of transcription 6 (STAT6). Since the IL4/STAT6 pathway reduces MÏ responsiveness to inflammation in a targeted and precise manner, IL4 delivery offers personalized possibilities to overcome inflammatory events. Despite its therapeutic potential, the limited success of IL4-targeted delivery is hampered by inefficient vehicles. Magnetically assisted technologies offer precise and tunable nanodevices for the delivery of cytokines by combining contactless modulation, high tissue penetration, imaging features, and low interference with the biological environment. Although superparamagnetic iron oxide nanoparticles (SPION) have shown clinical applicability in imaging, SPION-based approaches have rarely been explored for targeted delivery and cell programming. Herein, we hypothesized that SPION-based carriers assist in efficient IL4 delivery to MÏ , favoring a pro-regenerative phenotype (M2Ï ). Our results confirmed the efficiency of SPION-IL4 and MÏ responsiveness to SPION-IL4 with evidence of STAT6-mediated polarization. SPION-IL4-treated MÏ showed increased expression of M2Ï associated-mediators (IL10, ARG1, CCL2, IL1Ra) when compared to the well-established soluble IL4. The ability of SPION-IL4 to direct MÏ polarization using sophisticated magnetic nanotools is valuable for resolving inflammation and assisting innovative strategies for chronic inflammatory conditions.
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spelling Controlling Macrophage Polarization to Modulate Inflammatory Cues Using Immune-Switch NanoparticlescytokinesInflammationmacrophagesmagnetically assisted technologiesSPIONtargeted deliveryScience & TechnologyThe persistence of inflammatory mediators in tissue niches significantly impacts regenerative outcomes and contributes to chronic diseases. Interleukin-4 (IL4) boosts pro-healing phenotypes in macrophages (MÏ ) and triggers the activation of signal transducer and activator of transcription 6 (STAT6). Since the IL4/STAT6 pathway reduces MÏ responsiveness to inflammation in a targeted and precise manner, IL4 delivery offers personalized possibilities to overcome inflammatory events. Despite its therapeutic potential, the limited success of IL4-targeted delivery is hampered by inefficient vehicles. Magnetically assisted technologies offer precise and tunable nanodevices for the delivery of cytokines by combining contactless modulation, high tissue penetration, imaging features, and low interference with the biological environment. Although superparamagnetic iron oxide nanoparticles (SPION) have shown clinical applicability in imaging, SPION-based approaches have rarely been explored for targeted delivery and cell programming. Herein, we hypothesized that SPION-based carriers assist in efficient IL4 delivery to MÏ , favoring a pro-regenerative phenotype (M2Ï ). Our results confirmed the efficiency of SPION-IL4 and MÏ responsiveness to SPION-IL4 with evidence of STAT6-mediated polarization. SPION-IL4-treated MÏ showed increased expression of M2Ï associated-mediators (IL10, ARG1, CCL2, IL1Ra) when compared to the well-established soluble IL4. The ability of SPION-IL4 to direct MÏ polarization using sophisticated magnetic nanotools is valuable for resolving inflammation and assisting innovative strategies for chronic inflammatory conditions.This research was funded by the European Research Council, Consolidator Grant Magtendon, grant number 772817. FCT-Fundação para a Ciência e a Tecnologia, grant number SFDH/BD/144816/2019. FCT-Fundação para a Ciência e a Tecnologia under the Scientific Employment Stimulus—Individual Call: 2020.01157.CEECIND.MDPIUniversidade do MinhoAlmeida, A. F.Miranda, M. S.Vinhas, Carla Adriana AraújoGonçalves, A IGomes, Manuela E.Rodrigues, Márcia T.2022-122022-12-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/1822/81138engAlmeida A. F., Miranda M. S., Vinhas A., Gonçalves A. I., Gomes M. E., Rodrigues M. T. Controlling Macrophage Polarization to Modulate Inflammatory Cues Using Immune-Switch Nanoparticles, International Journal o f Molecular Sciences, Vol. 23, Issue 23, doi:10.3390/ijms232315125, 20221661-65961422-006710.3390/ijms23231512536499452https://www.mdpi.com/1422-0067/23/23/15125info: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:RCAAP2023-07-21T12:10:28Zoai:repositorium.sdum.uminho.pt:1822/81138Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T19:02:07.543486Repositório 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 Controlling Macrophage Polarization to Modulate Inflammatory Cues Using Immune-Switch Nanoparticles
title Controlling Macrophage Polarization to Modulate Inflammatory Cues Using Immune-Switch Nanoparticles
spellingShingle Controlling Macrophage Polarization to Modulate Inflammatory Cues Using Immune-Switch Nanoparticles
Almeida, A. F.
cytokines
Inflammation
macrophages
magnetically assisted technologies
SPION
targeted delivery
Science & Technology
title_short Controlling Macrophage Polarization to Modulate Inflammatory Cues Using Immune-Switch Nanoparticles
title_full Controlling Macrophage Polarization to Modulate Inflammatory Cues Using Immune-Switch Nanoparticles
title_fullStr Controlling Macrophage Polarization to Modulate Inflammatory Cues Using Immune-Switch Nanoparticles
title_full_unstemmed Controlling Macrophage Polarization to Modulate Inflammatory Cues Using Immune-Switch Nanoparticles
title_sort Controlling Macrophage Polarization to Modulate Inflammatory Cues Using Immune-Switch Nanoparticles
author Almeida, A. F.
author_facet Almeida, A. F.
Miranda, M. S.
Vinhas, Carla Adriana Araújo
Gonçalves, A I
Gomes, Manuela E.
Rodrigues, Márcia T.
author_role author
author2 Miranda, M. S.
Vinhas, Carla Adriana Araújo
Gonçalves, A I
Gomes, Manuela E.
Rodrigues, Márcia T.
author2_role author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade do Minho
dc.contributor.author.fl_str_mv Almeida, A. F.
Miranda, M. S.
Vinhas, Carla Adriana Araújo
Gonçalves, A I
Gomes, Manuela E.
Rodrigues, Márcia T.
dc.subject.por.fl_str_mv cytokines
Inflammation
macrophages
magnetically assisted technologies
SPION
targeted delivery
Science & Technology
topic cytokines
Inflammation
macrophages
magnetically assisted technologies
SPION
targeted delivery
Science & Technology
description The persistence of inflammatory mediators in tissue niches significantly impacts regenerative outcomes and contributes to chronic diseases. Interleukin-4 (IL4) boosts pro-healing phenotypes in macrophages (MÏ ) and triggers the activation of signal transducer and activator of transcription 6 (STAT6). Since the IL4/STAT6 pathway reduces MÏ responsiveness to inflammation in a targeted and precise manner, IL4 delivery offers personalized possibilities to overcome inflammatory events. Despite its therapeutic potential, the limited success of IL4-targeted delivery is hampered by inefficient vehicles. Magnetically assisted technologies offer precise and tunable nanodevices for the delivery of cytokines by combining contactless modulation, high tissue penetration, imaging features, and low interference with the biological environment. Although superparamagnetic iron oxide nanoparticles (SPION) have shown clinical applicability in imaging, SPION-based approaches have rarely been explored for targeted delivery and cell programming. Herein, we hypothesized that SPION-based carriers assist in efficient IL4 delivery to MÏ , favoring a pro-regenerative phenotype (M2Ï ). Our results confirmed the efficiency of SPION-IL4 and MÏ responsiveness to SPION-IL4 with evidence of STAT6-mediated polarization. SPION-IL4-treated MÏ showed increased expression of M2Ï associated-mediators (IL10, ARG1, CCL2, IL1Ra) when compared to the well-established soluble IL4. The ability of SPION-IL4 to direct MÏ polarization using sophisticated magnetic nanotools is valuable for resolving inflammation and assisting innovative strategies for chronic inflammatory conditions.
publishDate 2022
dc.date.none.fl_str_mv 2022-12
2022-12-01T00:00:00Z
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/1822/81138
url https://hdl.handle.net/1822/81138
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Almeida A. F., Miranda M. S., Vinhas A., Gonçalves A. I., Gomes M. E., Rodrigues M. T. Controlling Macrophage Polarization to Modulate Inflammatory Cues Using Immune-Switch Nanoparticles, International Journal o f Molecular Sciences, Vol. 23, Issue 23, doi:10.3390/ijms232315125, 2022
1661-6596
1422-0067
10.3390/ijms232315125
36499452
https://www.mdpi.com/1422-0067/23/23/15125
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 MDPI
publisher.none.fl_str_mv MDPI
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
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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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