Peroxisome proliferator-activated receptor alpha is required for feedback regulation of highly unsaturated fatty acid synthesis

J Lipid Res. 2005 Nov;46(11):2432-40. doi: 10.1194/jlr.M500237-JLR200. Epub 2005 Aug 16.

Abstract

Delta6 desaturase (D6D), the rate-limiting enzyme for highly unsaturated fatty acid (HUFA) synthesis, is induced by essential fatty acid-deficient diets. Sterol regulatory element-binding protein-1c (SREBP-1c) in part mediates this induction. Paradoxically, D6D is also induced by ligands of peroxisome proliferator-activated receptor alpha (PPARalpha). Here, we report a novel physiological role of PPARalpha in the induction of genes specific for HUFA synthesis by essential fatty acid-deficient diets. D6D mRNA induction by essential fatty acid-deficient diets in wild-type mice was diminished in PPARalpha-null mice. This impaired D6D induction in PPARalpha-null mice was not attributable to feedback suppression by tissue HUFAs because PPARalpha-null mice had lower HUFAs in liver phospholipids than did wild-type mice. Furthermore, PPARalpha-responsive genes were induced in wild-type mice under essential fatty acid deficiency, suggesting the generation of endogenous PPARalpha ligand(s). Contrary to genes for HUFA synthesis, the induction of other lipogenic genes under essential fatty acid deficiency was higher in PPARalpha-null mice than in wild-type mice even though mature SREBP-1c protein did not differ between the genotypes. The expression of PPARgamma was markedly increased in PPARalpha-null mice and might have contributed to the induction of genes for de novo lipogenesis. Our study suggests that PPARalpha, together with SREBP-1c, senses HUFA status and confers pathway-specific induction of HUFA synthesis by essential fatty acid-deficient diets.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arachidonic Acid / metabolism
  • Body Weight
  • Docosahexaenoic Acids / metabolism
  • Fatty Acid Desaturases
  • Fatty Acids / metabolism
  • Fatty Acids, Unsaturated / metabolism*
  • Feedback, Physiological*
  • Gene Expression Regulation, Enzymologic
  • Genotype
  • Ligands
  • Linoleoyl-CoA Desaturase / metabolism
  • Liver / metabolism
  • Mice
  • Mice, Transgenic
  • Microsomes / metabolism
  • Models, Statistical
  • PPAR alpha / genetics
  • PPAR alpha / metabolism
  • PPAR alpha / physiology*
  • RNA / metabolism
  • RNA, Messenger / metabolism
  • Sterol Regulatory Element Binding Protein 1 / metabolism
  • Transcription, Genetic

Substances

  • Fatty Acids
  • Fatty Acids, Unsaturated
  • Ligands
  • PPAR alpha
  • RNA, Messenger
  • Sterol Regulatory Element Binding Protein 1
  • Docosahexaenoic Acids
  • Arachidonic Acid
  • RNA
  • Fatty Acid Desaturases
  • Linoleoyl-CoA Desaturase