Controlling Macrophage Polarization to Modulate Inflammatory Cues Using Immune-Switch Nanoparticles
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , |
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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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 |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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