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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0022567,
umls-concept:C0023688,
umls-concept:C0076930,
umls-concept:C0086418,
umls-concept:C0086597,
umls-concept:C0205228,
umls-concept:C0332291,
umls-concept:C0442027,
umls-concept:C0542560,
umls-concept:C0851285,
umls-concept:C0871261,
umls-concept:C1511938,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C2911692
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pubmed:issue |
3
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pubmed:dateCreated |
1994-3-18
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pubmed:abstractText |
This study examined the expression of TGF-beta cell-surface receptors, the response to exogenous TGF-beta 1 and the autocrine production of TGF-beta in normal and squamous cell carcinoma-derived human oral keratinocytes with variable degrees of cellular differentiation. TGF-beta receptor expression, the response to exogenous ligand and the autocrine production of TGF-beta appeared unrelated to cellular differentiation. Cells expressed variable proportions of type-I, -II and -III TGF-beta receptors. The expression of type-III receptors correlated inversely with the expression of type-I receptors, but there was no relationship between type-II and either type-I or type-III TGF-beta receptors. Normal cells and the majority (7 of 8) of tumour-derived keratinocytes were inhibited by exogenous TGF-beta 1 and the degree of inhibition correlated with the expression of type-I, but not type-II or type-III, TGF-beta receptors. One tumour-derived cell line was refractory to exogenous TGF-beta 1 although it expressed all 3 receptor types. Endogenous TGF-beta was produced by both normal and tumour-derived keratinocytes and correlated inversely to the expression of type-I, but not type-II, TGF-beta receptors. Further, cells that produced more autocrine TGF-beta had a diminished response to exogenous TGF-beta 1. The data indicate a complex interaction between the expression of TGF-beta cell-surface receptors, endogenous ligand production and the cellular response to exogenous TGF-beta 1.
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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/Culture Media, Conditioned,
http://linkedlifedata.com/resource/pubmed/chemical/Keratins,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Transforming Growth...,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta,
http://linkedlifedata.com/resource/pubmed/chemical/Vimentin
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
0020-7136
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
1
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pubmed:volume |
56
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
406-12
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pubmed:dateRevised |
2007-7-24
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pubmed:meshHeading |
pubmed-meshheading:7508893-3T3 Cells,
pubmed-meshheading:7508893-Animals,
pubmed-meshheading:7508893-Carcinoma, Squamous Cell,
pubmed-meshheading:7508893-Cell Differentiation,
pubmed-meshheading:7508893-Cell Line,
pubmed-meshheading:7508893-Culture Media, Conditioned,
pubmed-meshheading:7508893-Humans,
pubmed-meshheading:7508893-Keratinocytes,
pubmed-meshheading:7508893-Keratins,
pubmed-meshheading:7508893-Mice,
pubmed-meshheading:7508893-Mouth Mucosa,
pubmed-meshheading:7508893-Mouth Neoplasms,
pubmed-meshheading:7508893-Receptors, Transforming Growth Factor beta,
pubmed-meshheading:7508893-Transforming Growth Factor beta,
pubmed-meshheading:7508893-Tumor Cells, Cultured,
pubmed-meshheading:7508893-Vimentin
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pubmed:year |
1994
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pubmed:articleTitle |
TGF-beta receptor regulation mediates the response to exogenous ligand but is independent of the degree of cellular differentiation in human oral keratinocytes.
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pubmed:affiliation |
Department of Oral Medicine, Pathology and Microbiology, University of Bristol, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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