Toll-like receptor 5- and lymphotoxin β receptor-dependent epithelial Ccl20 expression involves the same NF-κB binding site but distinct NF-κB pathways and dynamics

Canonical and alternative NF-κB pathways depend on distinct NF-κB members and regulate expression of different gene subset in inflammatory and steady state conditions, respectively. In intestinal epithelial cells, both pathways control the transcription of the gene coding the CCL20 chemokine. Lympho...

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Autores principales: Sirard, Jean-Claude, Didierlaurent, Arnaud, Cayet, Delphine, Sierro, Frédéric, Rumbo, Martín
Formato: Articulo
Lenguaje:Inglés
Publicado: 2009
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Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/128906
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id I19-R120-10915-128906
record_format dspace
institution Universidad Nacional de La Plata
institution_str I-19
repository_str R-120
collection SEDICI (UNLP)
language Inglés
topic Ciencias Exactas
Medicina
NF-kappa-B
Toll-like receptor
Lymphotoxin beta
Chemokine
CCL20
spellingShingle Ciencias Exactas
Medicina
NF-kappa-B
Toll-like receptor
Lymphotoxin beta
Chemokine
CCL20
Sirard, Jean-Claude
Didierlaurent, Arnaud
Cayet, Delphine
Sierro, Frédéric
Rumbo, Martín
Toll-like receptor 5- and lymphotoxin β receptor-dependent epithelial Ccl20 expression involves the same NF-κB binding site but distinct NF-κB pathways and dynamics
topic_facet Ciencias Exactas
Medicina
NF-kappa-B
Toll-like receptor
Lymphotoxin beta
Chemokine
CCL20
description Canonical and alternative NF-κB pathways depend on distinct NF-κB members and regulate expression of different gene subset in inflammatory and steady state conditions, respectively. In intestinal epithelial cells, both pathways control the transcription of the gene coding the CCL20 chemokine. Lymphotoxin β receptor (LTβR) mediates long lasting CCL20 expression whereas Toll-like receptor 5 (TLR5) signals promote inducible and transient activation. Here, we investigated whether the regulation of CCL20 expression involves different promoter sites and NF-κB molecules in response to TLR5 and LTβR stimulation. In epithelial cells, both stimulation required the same promoter regions, especially the NF-κB binding site but involved different NF-κB isoforms: p65/p50 and p52/RelB, for TLR5 and LTβR-dependent activation, respectively. The dynamic of activation and interaction with CCL20-specific NF-κB site correlated with gene transcription. Similar Ccl20 expression and NF-κB activation was found in the small intestine of mice stimulated with TLR5 and LTβR agonists. In summary, different NF-κB pathways modulate CCL20 transcription by operating on the same NF-κB binding site in the same cell type.
format Articulo
Articulo
author Sirard, Jean-Claude
Didierlaurent, Arnaud
Cayet, Delphine
Sierro, Frédéric
Rumbo, Martín
author_facet Sirard, Jean-Claude
Didierlaurent, Arnaud
Cayet, Delphine
Sierro, Frédéric
Rumbo, Martín
author_sort Sirard, Jean-Claude
title Toll-like receptor 5- and lymphotoxin β receptor-dependent epithelial Ccl20 expression involves the same NF-κB binding site but distinct NF-κB pathways and dynamics
title_short Toll-like receptor 5- and lymphotoxin β receptor-dependent epithelial Ccl20 expression involves the same NF-κB binding site but distinct NF-κB pathways and dynamics
title_full Toll-like receptor 5- and lymphotoxin β receptor-dependent epithelial Ccl20 expression involves the same NF-κB binding site but distinct NF-κB pathways and dynamics
title_fullStr Toll-like receptor 5- and lymphotoxin β receptor-dependent epithelial Ccl20 expression involves the same NF-κB binding site but distinct NF-κB pathways and dynamics
title_full_unstemmed Toll-like receptor 5- and lymphotoxin β receptor-dependent epithelial Ccl20 expression involves the same NF-κB binding site but distinct NF-κB pathways and dynamics
title_sort toll-like receptor 5- and lymphotoxin β receptor-dependent epithelial ccl20 expression involves the same nf-κb binding site but distinct nf-κb pathways and dynamics
publishDate 2009
url http://sedici.unlp.edu.ar/handle/10915/128906
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