Source:http://linkedlifedata.com/resource/pubmed/id/15265695
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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
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| pubmed:dateCreated |
2004-7-21
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| pubmed:abstractText |
Transforming growth factor beta (TGFbeta) is a multifunctional cytokine with effects on many cell types. We recently showed that in addition to epithelial barrier enhancing properties, TGFbeta causes diminished cAMP-driven chloride secretion in colonic epithelia, in a manner that is p38 MAPK-dependent. In this study, we sought to further delineate the mechanism behind TGFbeta diminution of chloride secretion. Using colonic and kidney epithelial cell lines, we found that exposure to TGFbeta causes dramatic changes in the expression and localization of the apical membrane chloride channel, cystic fibrosis transmembrane conductance regulator (CFTR). In TGFbeta-treated colonic epithelia (T84 and HT-29), CFTR mRNA was significantly reduced 2-24 h post-cytokine exposure. At a time consistent with decreased colonic epithelial secretory responses (16 h), TGFbeta treatment caused diminished intracellular CFTR protein expression (confocal microscopy) and reduced channel expression in the apical membrane during stimulated chloride secretion (biotinylation assay). In comparison, polarized kidney epithelia (MDCK) treated with TGFbeta displayed similarly reduced secretory responses to cAMP stimulating agents; however, a perinuclear accumulation of CFTR was observed, contrasting the diffuse cytoplasmic CFTR expression of control cells. Our data indicate that TGFbeta has profound effects on the expression and subcellular localization of an important channel involved in cAMP-driven chloride secretion, and thus suggest TGFbeta represents a key regulator of fluid movement.
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| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:citationSubset |
IM
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| pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/CFTR protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Chlorides,
http://linkedlifedata.com/resource/pubmed/chemical/Cyclic AMP,
http://linkedlifedata.com/resource/pubmed/chemical/Cystic Fibrosis Transmembrane...,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta
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| pubmed:status |
MEDLINE
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| pubmed:month |
Aug
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| pubmed:issn |
0014-4827
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| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
15
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| pubmed:volume |
298
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
473-84
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| pubmed:dateRevised |
2006-11-15
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| pubmed:meshHeading |
pubmed-meshheading:15265695-Animals,
pubmed-meshheading:15265695-Cell Line,
pubmed-meshheading:15265695-Cell Membrane,
pubmed-meshheading:15265695-Cell Membrane Permeability,
pubmed-meshheading:15265695-Cell Nucleus,
pubmed-meshheading:15265695-Chlorides,
pubmed-meshheading:15265695-Cyclic AMP,
pubmed-meshheading:15265695-Cystic Fibrosis Transmembrane Conductance Regulator,
pubmed-meshheading:15265695-Cytoplasm,
pubmed-meshheading:15265695-Cytoskeleton,
pubmed-meshheading:15265695-Dogs,
pubmed-meshheading:15265695-Dose-Response Relationship, Drug,
pubmed-meshheading:15265695-Down-Regulation,
pubmed-meshheading:15265695-Epithelial Cells,
pubmed-meshheading:15265695-Humans,
pubmed-meshheading:15265695-Protein Transport,
pubmed-meshheading:15265695-RNA, Messenger,
pubmed-meshheading:15265695-Reaction Time,
pubmed-meshheading:15265695-Transforming Growth Factor beta,
pubmed-meshheading:15265695-Water-Electrolyte Balance
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| pubmed:year |
2004
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| pubmed:articleTitle |
TGFbeta down-regulation of the CFTR: a means to limit epithelial chloride secretion.
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| pubmed:affiliation |
Intestinal Disease Research Programme, Department of Pathology and Molecular Medicine, McMaster University, HSC-3N5C, Hamilton, Ontario, Canada L8N 3Z5.
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| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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