Source:http://linkedlifedata.com/resource/pubmed/id/17359298
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
2007-3-15
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pubmed:abstractText |
Embryonic stem (ES) cells and embryonal carcinoma (EC) cells express high amounts of functional connexin43 (Cx43). During mesoderm formation and subsequent cardiac differentiation, Cx43 is initially down-regulated but is up-regulated again as the emerging cardiomyocytes mature. In this study, we investigated the regulation of Cx43 expression during early phases of differentiation in F9 and P19 EC cells. We found a striking inverse correlation between the expression of Cx43 and that of the transcriptional repressor Snail1. No clear relationship was found with Smad-interacting-protein1 (SIP1), another transcription factor inducing epithelium-to-mesenchyme transition (EMT). Promoter-reporter assays indicated Cx43 repression at the promoter level by ectopically expressed Snail1. To establish whether the Cx43 down-regulation depends on endogenous Snail1, MES-1 cells, differentiated derivatives of P19 EC, were stably transfected by an siRNA construct silencing Snail1 expression. This resulted in a mesenchyme-to-epithelium transition, which was accompanied by increased levels of Cx43 mRNA and protein and enhanced metabolic and electrical coupling. We conclude that Snail1-mediated EMT results in a Cx43 repression.
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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/Connexin 43,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Messenger,
http://linkedlifedata.com/resource/pubmed/chemical/RNA, Small Interfering,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors,
http://linkedlifedata.com/resource/pubmed/chemical/snail family transcription factors
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0301-4681
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pubmed:author |
pubmed-author:BierhuizenMarti F AMF,
pubmed-author:BoonenKristel J MKJ,
pubmed-author:DoevendansPieter APA,
pubmed-author:KokBartB,
pubmed-author:RookMartin BMB,
pubmed-author:VosMarc AMA,
pubmed-author:de BakkerJacques M TJM,
pubmed-author:de BoerTeun PTP,
pubmed-author:van VeenToon A BTA,
pubmed-author:van der HeydenMarcel A GMA
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pubmed:issnType |
Print
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pubmed:volume |
75
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
208-18
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:17359298-Animals,
pubmed-meshheading:17359298-Carcinoma, Embryonal,
pubmed-meshheading:17359298-Cell Line, Tumor,
pubmed-meshheading:17359298-Connexin 43,
pubmed-meshheading:17359298-Down-Regulation,
pubmed-meshheading:17359298-Embryonic Stem Cells,
pubmed-meshheading:17359298-Epithelium,
pubmed-meshheading:17359298-Fluorescent Antibody Technique,
pubmed-meshheading:17359298-Gene Silencing,
pubmed-meshheading:17359298-Mesoderm,
pubmed-meshheading:17359298-Mice,
pubmed-meshheading:17359298-Promoter Regions, Genetic,
pubmed-meshheading:17359298-RNA, Messenger,
pubmed-meshheading:17359298-RNA, Small Interfering,
pubmed-meshheading:17359298-Transcription Factors,
pubmed-meshheading:17359298-Transfection
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pubmed:year |
2007
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pubmed:articleTitle |
Connexin43 repression following epithelium-to-mesenchyme transition in embryonal carcinoma cells requires Snail1 transcription factor.
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pubmed:affiliation |
Department of Medical Physiology, University Medical Center Utrecht, Yalelaan 50, 3584 CM Utrecht, The Netherlands.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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