Premium
Nuclear receptors in lipid metabolism and immunity
Author(s) -
Tontonoz Peter
Publication year - 2008
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.22.1_supplement.531.2
Subject(s) - adipogenesis , nuclear receptor , peroxisome proliferator activated receptor , wnt signaling pathway , thiazolidinedione , regulator , receptor , microbiology and biotechnology , lipid metabolism , adipocyte , chemistry , adipose tissue , biology , pharmacology , signal transduction , biochemistry , endocrinology , transcription factor , type 2 diabetes , gene , diabetes mellitus
PPARγ is the master regulator of adipogenesis and the molecular target of the thiazolidinedione anti‐diabetic drugs. By screening for compounds that promote adipogenesis, we identified a small molecule that targets the PPARγ pathway by a distinct mechanism. This molecule, harmine, is not a ligand for the receptor; rather, it acts as a cell type‐selective regulator of PPARγ expression. Administration of harmine to diabetic mice mimics the effects of PPARγ ligands on adipocyte gene expression and insulin sensitivity. Unlike thiazolidinediones, however, harmine does not cause significant weight gain or hepatic lipid accumulation. Molecular studies indicate that harmine controls PPARγ expression through inhibition of the Wnt signaling pathway. This work validates phenotypic screening of adipocytes as promising strategy for the identification of bioactive small molecules and suggests that regulators of PPARγ expression may represent a complementary approach to PPARγ ligands in the treatment of insulin resistance.