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PMID: 18518822 Published · ppublish English Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Review

Fat and beyond: the diverse biology of PPARgamma.

Annual review of biochemistry ·Vol. 77 ·2008-00-00 ·Pages 289-312

Tontonoz P, Spiegelman BM

Abstract

The nuclear receptor PPARgamma is a ligand-activated transcription factor that plays an important role in the control of gene expression linked to a variety of physiological processes. PPARgamma was initially characterized as the master regulator for the development of adipose cells. Ligands for PPARgamma include naturally occurring fatty acids and the thiazolidinedione (TZD) class of antidiabetic drugs. Activation of PPARgamma improves insulin sensitivity in rodents and humans through a combination of metabolic actions, including partitioning of lipid stores and the regulation of metabolic and inflammatory mediators termed adipokines. PPARgamma signaling has also been implicated in the control of cell proliferation, atherosclerosis, macrophage function, and immunity. Here, we review recent advances in our understanding of the diverse biological actions of PPARgamma with an eye toward the expanding therapeutic potential of PPARgamma agonist drugs.

MeSH Terms
Adipocytes/cytology Adipogenesis Animals Cell Nucleus/metabolism Humans Inflammation Insulin Resistance Macrophages/cytology Models, Biological Models, Molecular Neoplasms/metabolism PPAR gamma/agonists,metabolism Protein Conformation Protein Structure, Tertiary Thiazolidinediones/chemistry
Chemicals
PPAR gamma Thiazolidinediones 2,4-thiazolidinedione
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Tontonoz Peter
Howard Hughes Medical Institute and Department of Pathology and Laboratory Medicine, University of California-Los Angeles, CA 90095, USA. ptontonoz@mednet.ucla.edu
Spiegelman Bruce M
Article Info
Journal
Annual review of biochemistry
Abbr.
Annu Rev Biochem
ISSN
0066-4154
Published
2008-00-00
Pages
289-312
Language
English
Region
United States
NLM ID
2985150R
Subset
IM
Grants
NHLBI NIH HHS · HL 66088 · United States
NIDDK NIH HHS · R37 DK 3140 · United States
Howard Hughes Medical Institute · United States
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