PPAR-gamma: adipogenic regulator and thiazolidinedione receptor - PubMed (original) (raw)
Review
PPAR-gamma: adipogenic regulator and thiazolidinedione receptor
B M Spiegelman. Diabetes. 1998 Apr.
Abstract
The past several years have seen an explosive increase in our understanding of the transcriptional basis of adipose cell differentiation. In particular, a key role has been illustrated for PPAR-gamma, a member of the nuclear hormone receptor superfamily. PPAR-gamma has also been recently identified as the major functional receptor for the thiazolidinedione class of insulin-sensitizing drugs. This review examines the evidence that has implicated this transcription factor in the processes of adipogenesis and systemic insulin action. In addition, several models are discussed that may explain how a single protein can be involved in these related but distinct physiological actions. I also point out several important areas where our knowledge is incomplete and more research is needed. Finally, I discuss how advances in our understanding of nuclear receptor function, particularly the docking of cofactors in a ligand-dependent fashion, should lead to improved drugs that utilize the PPAR-gamma system for the treatment of insulin resistance.
Similar articles
- An antidiabetic thiazolidinedione is a high affinity ligand for peroxisome proliferator-activated receptor gamma (PPAR gamma).
Lehmann JM, Moore LB, Smith-Oliver TA, Wilkison WO, Willson TM, Kliewer SA. Lehmann JM, et al. J Biol Chem. 1995 Jun 2;270(22):12953-6. doi: 10.1074/jbc.270.22.12953. J Biol Chem. 1995. PMID: 7768881 - Experimental approaches to study PPAR gamma agonists as antidiabetic drugs.
Vázquez M, Silvestre JS, Prous JR. Vázquez M, et al. Methods Find Exp Clin Pharmacol. 2002 Oct;24(8):515-23. doi: 10.1358/mf.2002.24.8.705072. Methods Find Exp Clin Pharmacol. 2002. PMID: 12500431 Review. - Novel insulin sensitizers: pharmacogenomic aspects.
Otto C, Lehrke M, Göke B. Otto C, et al. Pharmacogenomics. 2002 Jan;3(1):99-116. doi: 10.1517/14622416.3.1.99. Pharmacogenomics. 2002. PMID: 11966407 Review. - Metabolic and additional vascular effects of thiazolidinediones.
Martens FM, Visseren FL, Lemay J, de Koning EJ, Rabelink TJ. Martens FM, et al. Drugs. 2002;62(10):1463-80. doi: 10.2165/00003495-200262100-00004. Drugs. 2002. PMID: 12093315 Review.
Cited by
- Transcription factor AP1 binds the functional region of the promoter and regulates gene expression of human PPARdelta in LoVo cell.
Jiang X, Yang X, Han Y, Lu S. Jiang X, et al. Tumour Biol. 2013 Dec;34(6):3619-25. doi: 10.1007/s13277-013-0943-4. Epub 2013 Jul 6. Tumour Biol. 2013. PMID: 23832539 - Adipocytes under assault: environmental disruption of adipose physiology.
Regnier SM, Sargis RM. Regnier SM, et al. Biochim Biophys Acta. 2014 Mar;1842(3):520-33. doi: 10.1016/j.bbadis.2013.05.028. Epub 2013 Jun 2. Biochim Biophys Acta. 2014. PMID: 23735214 Free PMC article. Review. - Tributyltin differentially promotes development of a phenotypically distinct adipocyte.
Regnier SM, El-Hashani E, Kamau W, Zhang X, Massad NL, Sargis RM. Regnier SM, et al. Obesity (Silver Spring). 2015 Sep;23(9):1864-71. doi: 10.1002/oby.21174. Epub 2015 Aug 4. Obesity (Silver Spring). 2015. PMID: 26243053 Free PMC article. - Regulation of small ubiquitin-like modifier-1, nuclear receptor coreceptor, histone deacetylase 3, and peroxisome proliferator-activated receptor-γ in human adipose tissue.
Finlin BS, Bodles-Brakhop AM, Yao-Borengasser A, Zhu B, Starnes CP, McGehee RE Jr, Peterson CA, Kern PA, Rasouli N. Finlin BS, et al. Metab Syndr Relat Disord. 2012 Aug;10(4):312-7. doi: 10.1089/met.2011.0121. Epub 2012 May 31. Metab Syndr Relat Disord. 2012. PMID: 22651256 Free PMC article. Clinical Trial. - Data-driven integration of epidemiological and toxicological data to select candidate interacting genes and environmental factors in association with disease.
Patel CJ, Chen R, Butte AJ. Patel CJ, et al. Bioinformatics. 2012 Jun 15;28(12):i121-6. doi: 10.1093/bioinformatics/bts229. Bioinformatics. 2012. PMID: 22689751 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
Miscellaneous