Peroxisome proliferator-activated receptors and lipid metabolism

Ann N Y Acad Sci. 1993 Jun 11:684:157-73. doi: 10.1111/j.1749-6632.1993.tb32279.x.

Abstract

PPARs are nuclear hormone receptors which, like the retinoid, thyroid hormone, vitamin D, and steroid hormone receptors, are ligand-activated transcription factors mediating the hormonal control of gene expression. Two lines of evidence indicate that PPARs have an important function in fatty acid metabolism. First, PPARs are activated by hypolipidemic drugs and physiological concentrations of fatty acids, and second, PPARs control the peroxisomal beta-oxidation pathway of fatty acids through transcriptional induction of the gene encoding the acyl-CoA oxidase (ACO), which is the rate-limiting enzyme of the pathway. Furthermore, the PPAR signaling pathway appears to converge with the 9-cis retinoic acid receptor (RXR) signaling pathway in the regulation of the ACO gene because heterodimerization between PPAR and RXR is essential for in vitro binding to the PPRE and because the strongest stimulation of this gene is observed when both receptors are exposed simultaneously to their activators. Thus, it appears that PPARs are involved in the 9-cis retinoic acid signaling pathway and that they play a pivotal role in the hormonal control of lipid metabolism.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Acyl-CoA Oxidase
  • Animals
  • Base Sequence
  • DNA
  • Fatty Acids / physiology
  • Humans
  • Hypolipidemic Agents / pharmacology
  • Lipid Metabolism*
  • Microbodies / metabolism
  • Molecular Sequence Data
  • Oxidoreductases / genetics
  • Oxidoreductases / metabolism
  • Receptors, Cell Surface / drug effects*
  • Receptors, Cell Surface / metabolism
  • Receptors, Cytoplasmic and Nuclear*
  • Signal Transduction
  • Transcription Factors / metabolism*

Substances

  • Fatty Acids
  • Hypolipidemic Agents
  • Receptors, Cell Surface
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • DNA
  • Oxidoreductases
  • Acyl-CoA Oxidase