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The nuclear receptor PPARgamma - bigger than fat
1Department of Molecular Endocrinology, Glaxo Wellcome Research and Development, Five Moore Drive, Research Triangle Park, North Carolina, 27709, USA. sak15922@glaxowellcome.com
Current Opinion in Genetics & Development
|October 31, 1998
Summary
Recent studies reveal how activating the nuclear receptor peroxisome proliferator-activated receptor gamma (PPARgamma) controls glucose and lipid balance. This receptor also plays roles in monocytes, cell cycles, and cancer, with fatty acids acting as key activators.
Area of Science:
- Endocrinology
- Molecular Biology
- Metabolic Regulation
Background:
- Peroxisome proliferator-activated receptor gamma (PPARgamma) is a nuclear receptor.
- PPARgamma plays a crucial role in regulating systemic glucose and lipid homeostasis.
- Emerging evidence implicates PPARgamma in monocyte biology, cell-cycle regulation, and cancer.
Purpose of the Study:
- To elucidate the mechanisms of ligand-activated PPARgamma in metabolic regulation.
- To explore the broader biological functions of PPARgamma beyond metabolic homeostasis.
- To investigate the role of specific lipids in activating PPARgamma.
Main Methods:
- Review of recent research findings on PPARgamma.
- Analysis of studies investigating ligand-receptor interactions.
- Examination of PPARgamma's involvement in cellular processes.
Main Results:
- Ligand activation of PPARgamma is a key mechanism for regulating glucose and lipid homeostasis.
- PPARgamma is involved in the biology of monocytes, influencing immune cell function.
- PPARgamma has implications in cell-cycle regulation and the development of cancer.
- Polyunsaturated fatty acids and eicosanoids are identified as endogenous ligands that bind and activate PPARgamma.
Conclusions:
- PPARgamma is a central regulator of metabolic processes.
- The functions of PPARgamma extend to immune cells and cancer biology.
- Lipids like polyunsaturated fatty acids and eicosanoids may act as hormonal regulators in diverse biological pathways.