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Release of IL-1β via IL-1β-Converting Enzyme in a Skin Dendritic Cell Line Exposed to 2,4-Dinitrofluorobenzene

We used a mouse fetal skin dendritic cell line (FSDC) to study the effect of the strong allergen 2,4-dinitrofluorobenzene (DNFB) on interleukin (IL)-1β release and IL-1β receptor immunoreactivity. Stimulation with DNFB (30 minutes) increased IL-1β release without changing the mRNA levels of the prot...

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Autores principales: Matos, Teresa J., Jaleco, Sara P., Gonçalo, Margarida, Duarte, Carlos B., Lopes, M. Celeste
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1526472/
https://www.ncbi.nlm.nih.gov/pubmed/16106098
http://dx.doi.org/10.1155/MI.2005.131
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author Matos, Teresa J.
Jaleco, Sara P.
Gonçalo, Margarida
Duarte, Carlos B.
Lopes, M. Celeste
author_facet Matos, Teresa J.
Jaleco, Sara P.
Gonçalo, Margarida
Duarte, Carlos B.
Lopes, M. Celeste
author_sort Matos, Teresa J.
collection PubMed
description We used a mouse fetal skin dendritic cell line (FSDC) to study the effect of the strong allergen 2,4-dinitrofluorobenzene (DNFB) on interleukin (IL)-1β release and IL-1β receptor immunoreactivity. Stimulation with DNFB (30 minutes) increased IL-1β release without changing the mRNA levels of the protein. Furthermore, DNFB increased transiently the interleukin-1β-converting enzyme (ICE) activity, as measured with its fluorogenic substrate Z-Tyr-Val-Ala-Asp-AFC. The ICE inhibitor Z-YVAD-FMK prevented the release of IL-1β evoked by DNFB. Incubation of the cells with DNFB (30 minutes) strongly increased IL-1β receptor immunoreactivity. The rapid effect of DNFB on the release of mature IL-1β, without inducing an increase of IL-1β mRNA in FSDC, suggests a posttranslational modification of pro-IL-1β by ICE activity.
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spelling pubmed-15264722006-08-21 Release of IL-1β via IL-1β-Converting Enzyme in a Skin Dendritic Cell Line Exposed to 2,4-Dinitrofluorobenzene Matos, Teresa J. Jaleco, Sara P. Gonçalo, Margarida Duarte, Carlos B. Lopes, M. Celeste Mediators Inflamm Research Communication We used a mouse fetal skin dendritic cell line (FSDC) to study the effect of the strong allergen 2,4-dinitrofluorobenzene (DNFB) on interleukin (IL)-1β release and IL-1β receptor immunoreactivity. Stimulation with DNFB (30 minutes) increased IL-1β release without changing the mRNA levels of the protein. Furthermore, DNFB increased transiently the interleukin-1β-converting enzyme (ICE) activity, as measured with its fluorogenic substrate Z-Tyr-Val-Ala-Asp-AFC. The ICE inhibitor Z-YVAD-FMK prevented the release of IL-1β evoked by DNFB. Incubation of the cells with DNFB (30 minutes) strongly increased IL-1β receptor immunoreactivity. The rapid effect of DNFB on the release of mature IL-1β, without inducing an increase of IL-1β mRNA in FSDC, suggests a posttranslational modification of pro-IL-1β by ICE activity. Hindawi Publishing Corporation 2005-08-14 /pmc/articles/PMC1526472/ /pubmed/16106098 http://dx.doi.org/10.1155/MI.2005.131 Text en Hindawi Publishing Corporation
spellingShingle Research Communication
Matos, Teresa J.
Jaleco, Sara P.
Gonçalo, Margarida
Duarte, Carlos B.
Lopes, M. Celeste
Release of IL-1β via IL-1β-Converting Enzyme in a Skin Dendritic Cell Line Exposed to 2,4-Dinitrofluorobenzene
title Release of IL-1β via IL-1β-Converting Enzyme in a Skin Dendritic Cell Line Exposed to 2,4-Dinitrofluorobenzene
title_full Release of IL-1β via IL-1β-Converting Enzyme in a Skin Dendritic Cell Line Exposed to 2,4-Dinitrofluorobenzene
title_fullStr Release of IL-1β via IL-1β-Converting Enzyme in a Skin Dendritic Cell Line Exposed to 2,4-Dinitrofluorobenzene
title_full_unstemmed Release of IL-1β via IL-1β-Converting Enzyme in a Skin Dendritic Cell Line Exposed to 2,4-Dinitrofluorobenzene
title_short Release of IL-1β via IL-1β-Converting Enzyme in a Skin Dendritic Cell Line Exposed to 2,4-Dinitrofluorobenzene
title_sort release of il-1β via il-1β-converting enzyme in a skin dendritic cell line exposed to 2,4-dinitrofluorobenzene
topic Research Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1526472/
https://www.ncbi.nlm.nih.gov/pubmed/16106098
http://dx.doi.org/10.1155/MI.2005.131
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