Source:http://linkedlifedata.com/resource/pubmed/id/10871190
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2000-7-6
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pubmed:abstractText |
The antidiabetic thiazolidinediones, which include troglitazone and rosiglitazone, are ligands for the nuclear receptor peroxisome proliferator-activated receptor (PPAR)-gamma and exert their antihyperglycemic effects by regulation of PPAR-gamma-responsive genes. We report here that PPAR-gamma activation by troglitazone depends on the experimental setting. Troglitazone acts as a partial agonist for PPAR-gamma in transfected muscle (C2C12) and kidney (HEK 293T) cells, producing a submaximal transcriptional response (1.8- to 2.5-fold activation) compared with rosiglitazone (7.4- to 13-fold activation). Additionally, troglitazone antagonizes rosiglitazone-stimulated PPAR-gamma transcriptional activity. Limited protease digestion of PPAR-gamma suggests conformational differences in the receptor bound to troglitazone versus rosiglitazone. Consistent with this finding, an in vitro coactivator association assay demonstrated that troglitazone-bound PPAR-gamma recruited the transcriptional coactivators p300 and steroid receptor coactivator 1 less efficiently than rosiglitazone-bound receptor. In contrast to these observations, troglitazone behaves as a full agonist of PPAR-gamma in 3T3L1 adipocytes. Two-dimensional protein gel electrophoresis demonstrated that troglitazone and rosiglitazone regulated distinct but overlapping sets of genes in several cell types. Thus, troglitazone may behave as a partial agonist under certain physiological circumstances and as a full agonist in others. These differences could be caused by variations in the amount of specific cofactors, differences in PPAR response elements, or the presence of different isoforms of PPAR-gamma.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Chromans,
http://linkedlifedata.com/resource/pubmed/chemical/Hypoglycemic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Cytoplasmic and Nuclear,
http://linkedlifedata.com/resource/pubmed/chemical/Thiazoles,
http://linkedlifedata.com/resource/pubmed/chemical/Thiazolidinediones,
http://linkedlifedata.com/resource/pubmed/chemical/Transcription Factors,
http://linkedlifedata.com/resource/pubmed/chemical/Trypsin,
http://linkedlifedata.com/resource/pubmed/chemical/rosiglitazone,
http://linkedlifedata.com/resource/pubmed/chemical/troglitazone
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pubmed:status |
MEDLINE
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pubmed:month |
Apr
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pubmed:issn |
0012-1797
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
49
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
539-47
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pubmed:dateRevised |
2004-11-17
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pubmed:meshHeading |
pubmed-meshheading:10871190-3T3 Cells,
pubmed-meshheading:10871190-Animals,
pubmed-meshheading:10871190-Cell Line,
pubmed-meshheading:10871190-Chromans,
pubmed-meshheading:10871190-Electrophoresis, Gel, Two-Dimensional,
pubmed-meshheading:10871190-Epithelial Cells,
pubmed-meshheading:10871190-Gene Expression Regulation,
pubmed-meshheading:10871190-Humans,
pubmed-meshheading:10871190-Hypoglycemic Agents,
pubmed-meshheading:10871190-Kidney,
pubmed-meshheading:10871190-Mice,
pubmed-meshheading:10871190-Receptors, Cytoplasmic and Nuclear,
pubmed-meshheading:10871190-Thiazoles,
pubmed-meshheading:10871190-Thiazolidinediones,
pubmed-meshheading:10871190-Transcription Factors,
pubmed-meshheading:10871190-Transfection,
pubmed-meshheading:10871190-Trypsin
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pubmed:year |
2000
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pubmed:articleTitle |
Differential activation of peroxisome proliferator-activated receptor-gamma by troglitazone and rosiglitazone.
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pubmed:affiliation |
Department of Cell Biology, Warner-Lambert Company, Ann Arbor, Michigan, USA.
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pubmed:publicationType |
Journal Article
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