Please use this identifier to cite or link to this item: http://sgc.anlis.gob.ar/handle/123456789/467
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dc.contributor.authorCafferata, Eduardoes
dc.contributor.authorGonzález Guerrico, Anatilde M.es
dc.contributor.authorPivetta, Omar H.es
dc.contributor.authorSanta-Coloma, Tomás A.es
dc.date.accessioned2013-04-03T01:09:41Z-
dc.date.available2013-04-03T01:09:41Z-
dc.date.issued2001-05-04-
dc.identifier.urihttp://sgc.anlis.gob.ar/handle/123456789/467-
dc.descriptionFil: Cafferata, Eduardo. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica Dr. Eduardo Castilla. Departamento de Genética Experimental; Argentina.es
dc.descriptionFil: González Guerrico, Anatilde M. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica Dr. Eduardo Castilla. Departamento de Genética Experimental; Argentina.es
dc.descriptionFil: Pivetta, Omar H. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica Dr. Eduardo Castilla. Departamento de Genética Experimental; Argentina.es
dc.descriptionFil: Santa-Coloma, Tomás A. ANLIS Dr.C.G.Malbrán. Centro Nacional de Genética Médica Dr. Eduardo Castilla. Departamento de Genética Experimental; Argentina.es
dc.description.abstractInterleukin-1 beta (IL-1 beta) regulates the levels of cystic fibrosis transmembrane conductance regulator (CFTR) mRNA and protein in the T84 human carcinoma cell line. Here, we studied the role of the transcription factor NF-kappaB in this regulation. Initially, T84 cells were pretreated with the NF-kappaB inhibitor pyrrolidine dithiocarbamate, Cells were then stimulated with IL-1 beta, and CFTR mRNA levels were determined after 4 h by Northern blot analysis. As a result of PDTC treatment, IL-1 beta stimulation of CFTR mRNA was blocked, On the other hand, daunorubicin, an NF-kappaB activator, increased the steady-state levels of CFTR mRNA, Furthermore, after treatment with IL-1 beta for 1 h, cytoplasmic I kappaB alpha degradation occurred simultaneously with translocation of p65 into the nucleus, The T84 cells were also transduced with an adenoviral vector expressing a dominant negative form of I kappaB alpha, which prevents I kappaB alpha phosphorylation and the subsequent nuclear translocation of NF-kappaB, After viral transduction, the cells were stimulated with IL-1 beta for 4 h, and CFTR mRNA levels were measured by Northern blot analysis. The stimulation of CFTR, induced by IL-1 beta, was also blocked in the presence of the dominant negative mutant. These results indicate that NF-kappaB is involved in the pathway by which IL-1 beta regulates CFTR.es
dc.language.isoenes
dc.relation.ispartofThe Journal of biological chemistryes
dc.rightsOpen Accessen_US
dc.rightsCreative Commons Attribution 4.0 International License-
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/-
dc.sourceJournal of Biological Chemistry 2001;276(18):15441-15444en_US
dc.subjectFibrosis Quísticaes
dc.subjectInterleucina-1betaes
dc.subjectRegulador de Conductancia de Transmembrana de Fibrosis Quísticaes
dc.subjectEnsayo de Cambio de Movilidad Electroforéticaes
dc.titleNF-kappa B activation is involved in regulation of cystic fibrosis transmembrane conductance regulator (CFTR) by interleukin-1 betaes
dc.typeArtículoes
dc.identifier.doi10.1074/jbc.M010061200-
anlis.essnrd1-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
item.grantfulltextopen-
item.openairetypeArtículo-
item.fulltextWith Fulltext-
item.languageiso639-1en-
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