Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
9
pubmed:dateCreated
2008-9-1
pubmed:abstractText
We previously identified the small molecule harmine as a regulator of peroxisome proliferator activated-receptor gamma (PPARgamma) and adipocyte differentiation. In an effort to identify signaling pathways mediating harmine's effects, we performed transcriptional profiling of 3T3-F442A preadipocytes. Inhibitor of DNA biding 2 (Id2) was identified as a gene rapidly induced by harmine but not by PPARgamma agonists. Id2 is also induced in 3T3-L1 preadipocytes treated with dexamethasone, 3-isobutyl-1-methylxanthine, and insulin, suggesting that Id2 regulation is a common feature of the adipogenic program. Stable overexpression of Id2 in preadipocytes promotes expression of PPARgamma and enhances morphological differentiation and lipid accumulation. Conversely, small interfering RNA-mediated knockdown of Id2 antagonizes adipocyte differentiation. Mice lacking Id2 expression display reduced adiposity, and embryonic fibroblasts derived from these mice exhibit reduced PPARgamma expression and a diminished capacity for adipocyte differentiation. Finally, Id2 expression is elevated in adipose tissues of obese mice and humans. These results outline a role for Id2 in the modulation of PPARgamma expression and adipogenesis and underscore the utility of adipogenic small molecules as tools to dissect adipocyte biology.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-10022839, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-10067894, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-10585876, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-10622252, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-10681562, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-10837022, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-10937998, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-11021798, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-12110166, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-12426306, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-12524424, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-12861022, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-12888293, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-15664998, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-16054042, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-16054051, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-16059715, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-16239924, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-17086188, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-17351296, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-17488638, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-17604724, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-7557387, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-7926730, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-8001151, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-8654925, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-8946919, http://linkedlifedata.com/resource/pubmed/commentcorrection/18562627-9405372
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Sep
pubmed:issn
0888-8809
pubmed:author
pubmed:issnType
Print
pubmed:volume
22
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
2038-48
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed-meshheading:18562627-3T3 Cells, pubmed-meshheading:18562627-3T3-L1 Cells, pubmed-meshheading:18562627-Adipocytes, pubmed-meshheading:18562627-Adipogenesis, pubmed-meshheading:18562627-Adiposity, pubmed-meshheading:18562627-Animals, pubmed-meshheading:18562627-Cell Differentiation, pubmed-meshheading:18562627-Gene Expression, pubmed-meshheading:18562627-Gene Expression Profiling, pubmed-meshheading:18562627-Harmine, pubmed-meshheading:18562627-Humans, pubmed-meshheading:18562627-Inhibitor of Differentiation Protein 2, pubmed-meshheading:18562627-Mice, pubmed-meshheading:18562627-Mice, Inbred C57BL, pubmed-meshheading:18562627-Mice, Obese, pubmed-meshheading:18562627-PPAR gamma, pubmed-meshheading:18562627-RNA Interference, pubmed-meshheading:18562627-Signal Transduction, pubmed-meshheading:18562627-Wnt Proteins
pubmed:year
2008
pubmed:articleTitle
Inhibitor of DNA binding 2 is a small molecule-inducible modulator of peroxisome proliferator-activated receptor-gamma expression and adipocyte differentiation.
pubmed:affiliation
Howard Hughes Medical Institute, University of California, Los Angeles, California 90095, USA.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't