Differential modulation of CXCR4 and CD40 protein levels by skin sensitizers and irritants in the FSDC cell line

Detalhes bibliográficos
Autor(a) principal: Neves, Bruno Miguel
Data de Publicação: 2008
Outros Autores: Cruz, Maria Teresa, Francisco, Vera, Gonçalo, Margarida, Figueiredo, Américo, Duarte, Carlos B., Lopes, Maria Celeste
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/5843
https://doi.org/10.1016/j.toxlet.2007.12.006
Resumo: The development of non-animal methods for skin sensitization testing is an urgent challenge. Some of the most promising in vitro approaches are based on the analysis of phenotypical and functional modifications induced by sensitizers in dendritic cell models. In this work, we evaluated, for the first time, a fetal skin-derived dendritic cell line (FSDC) as a model to discriminate between sensitizers and irritants, through analysis of their effects on CD40 and CXCR4 protein expression. The chemicals concentrations were chosen based on a slight cytotoxicity effect (up to 15%). Protein levels were evaluated by Western blot and immunocytochemistry, after stimulation with the skin sensitizers 2,4-dinitrofluorobenzene (DNFB), 1,4-phenylenediamine (PPD) and nickel sulphate (NiSO4), the non-sensitizer 2,4-dichloronitrobenzene (DCNB), and the irritants sodium dodecyl sulphate (SDS) and benzalkonium chloride (BC). All sensitizers tested increased CD40 and CXCR4 levels. In contrast, irritants decreased both proteins levels, with a more pronounced effect on CXCR4. In agreement with these results, dendritic cells derived from human peripheral blood monocytes-derived dendritic cells (MoDC) showed a similar response pattern to the skin sensitizer and irritant tested, PPD and SDS, respectively. In conclusion, evaluation of CD40 and CXCR4 proteins in chemical-treated FSDC may represent a useful tool in a future in vitro test for sensitizing assessment.
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spelling Differential modulation of CXCR4 and CD40 protein levels by skin sensitizers and irritants in the FSDC cell lineIn vitro sensitization testFSDC cell lineCXCR4CD40The development of non-animal methods for skin sensitization testing is an urgent challenge. Some of the most promising in vitro approaches are based on the analysis of phenotypical and functional modifications induced by sensitizers in dendritic cell models. In this work, we evaluated, for the first time, a fetal skin-derived dendritic cell line (FSDC) as a model to discriminate between sensitizers and irritants, through analysis of their effects on CD40 and CXCR4 protein expression. The chemicals concentrations were chosen based on a slight cytotoxicity effect (up to 15%). Protein levels were evaluated by Western blot and immunocytochemistry, after stimulation with the skin sensitizers 2,4-dinitrofluorobenzene (DNFB), 1,4-phenylenediamine (PPD) and nickel sulphate (NiSO4), the non-sensitizer 2,4-dichloronitrobenzene (DCNB), and the irritants sodium dodecyl sulphate (SDS) and benzalkonium chloride (BC). All sensitizers tested increased CD40 and CXCR4 levels. In contrast, irritants decreased both proteins levels, with a more pronounced effect on CXCR4. In agreement with these results, dendritic cells derived from human peripheral blood monocytes-derived dendritic cells (MoDC) showed a similar response pattern to the skin sensitizer and irritant tested, PPD and SDS, respectively. In conclusion, evaluation of CD40 and CXCR4 proteins in chemical-treated FSDC may represent a useful tool in a future in vitro test for sensitizing assessment.2008info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleaplication/PDFhttp://hdl.handle.net/10316/5843http://hdl.handle.net/10316/5843https://doi.org/10.1016/j.toxlet.2007.12.006engToxicology Letters. 177:1 (2008) 74-82Neves, Bruno MiguelCruz, Maria TeresaFrancisco, VeraGonçalo, MargaridaFigueiredo, AméricoDuarte, Carlos B.Lopes, Maria Celesteinfo: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:RCAAP2022-05-25T03:34:33Zoai:estudogeral.uc.pt:10316/5843Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:47:25.461567Repositório 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 Differential modulation of CXCR4 and CD40 protein levels by skin sensitizers and irritants in the FSDC cell line
title Differential modulation of CXCR4 and CD40 protein levels by skin sensitizers and irritants in the FSDC cell line
spellingShingle Differential modulation of CXCR4 and CD40 protein levels by skin sensitizers and irritants in the FSDC cell line
Neves, Bruno Miguel
In vitro sensitization test
FSDC cell line
CXCR4
CD40
title_short Differential modulation of CXCR4 and CD40 protein levels by skin sensitizers and irritants in the FSDC cell line
title_full Differential modulation of CXCR4 and CD40 protein levels by skin sensitizers and irritants in the FSDC cell line
title_fullStr Differential modulation of CXCR4 and CD40 protein levels by skin sensitizers and irritants in the FSDC cell line
title_full_unstemmed Differential modulation of CXCR4 and CD40 protein levels by skin sensitizers and irritants in the FSDC cell line
title_sort Differential modulation of CXCR4 and CD40 protein levels by skin sensitizers and irritants in the FSDC cell line
author Neves, Bruno Miguel
author_facet Neves, Bruno Miguel
Cruz, Maria Teresa
Francisco, Vera
Gonçalo, Margarida
Figueiredo, Américo
Duarte, Carlos B.
Lopes, Maria Celeste
author_role author
author2 Cruz, Maria Teresa
Francisco, Vera
Gonçalo, Margarida
Figueiredo, Américo
Duarte, Carlos B.
Lopes, Maria Celeste
author2_role author
author
author
author
author
author
dc.contributor.author.fl_str_mv Neves, Bruno Miguel
Cruz, Maria Teresa
Francisco, Vera
Gonçalo, Margarida
Figueiredo, Américo
Duarte, Carlos B.
Lopes, Maria Celeste
dc.subject.por.fl_str_mv In vitro sensitization test
FSDC cell line
CXCR4
CD40
topic In vitro sensitization test
FSDC cell line
CXCR4
CD40
description The development of non-animal methods for skin sensitization testing is an urgent challenge. Some of the most promising in vitro approaches are based on the analysis of phenotypical and functional modifications induced by sensitizers in dendritic cell models. In this work, we evaluated, for the first time, a fetal skin-derived dendritic cell line (FSDC) as a model to discriminate between sensitizers and irritants, through analysis of their effects on CD40 and CXCR4 protein expression. The chemicals concentrations were chosen based on a slight cytotoxicity effect (up to 15%). Protein levels were evaluated by Western blot and immunocytochemistry, after stimulation with the skin sensitizers 2,4-dinitrofluorobenzene (DNFB), 1,4-phenylenediamine (PPD) and nickel sulphate (NiSO4), the non-sensitizer 2,4-dichloronitrobenzene (DCNB), and the irritants sodium dodecyl sulphate (SDS) and benzalkonium chloride (BC). All sensitizers tested increased CD40 and CXCR4 levels. In contrast, irritants decreased both proteins levels, with a more pronounced effect on CXCR4. In agreement with these results, dendritic cells derived from human peripheral blood monocytes-derived dendritic cells (MoDC) showed a similar response pattern to the skin sensitizer and irritant tested, PPD and SDS, respectively. In conclusion, evaluation of CD40 and CXCR4 proteins in chemical-treated FSDC may represent a useful tool in a future in vitro test for sensitizing assessment.
publishDate 2008
dc.date.none.fl_str_mv 2008
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/5843
http://hdl.handle.net/10316/5843
https://doi.org/10.1016/j.toxlet.2007.12.006
url http://hdl.handle.net/10316/5843
https://doi.org/10.1016/j.toxlet.2007.12.006
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Toxicology Letters. 177:1 (2008) 74-82
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