Peroxisome proliferator-activated receptor γ-dependent regulation of lipolytic nodes and metabolic flexibility

Mol Cell Biol. 2012 Apr;32(8):1555-65. doi: 10.1128/MCB.06154-11. Epub 2012 Feb 6.

Abstract

Optimal lipid storage and mobilization are essential for efficient adipose tissue. Nuclear receptor peroxisome proliferator-activated receptor γ (PPARγ) regulates adipocyte differentiation and lipid deposition, but its role in lipolysis and dysregulation in obesity is not well defined. This investigation aimed to understand the molecular impact of dysfunctional PPARγ on the lipolytic axis and to explore whether these defects are also confirmed in common forms of human obesity. For this purpose, we used the P465L PPARγ mouse as a model of dysfunctional PPARγ that recapitulates the human pparγ mutation (P467L). We demonstrated that defective PPARγ impairs catecholamine-induced lipolysis. This abnormal lipolytic response is exacerbated by a state of positive energy balance in leptin-deficient ob/ob mice. We identified the protein kinase A (PKA) network as a PPARγ-dependent regulatory node of the lipolytic response. Specifically, defective PPARγ is associated with decreased basal expression of prkaca (PKAcatα) and d-akap1, the lipase genes Pnplaz (ATGL) and Lipe (HSL), and lipid droplet protein genes fsp27 and adrp in vivo and in vitro. Our data indicate that PPARγ is required for activation of the lipolytic regulatory network, dysregulation of which is an important feature of obesity-induced insulin resistance in humans.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Catecholamines / metabolism
  • Cyclic AMP-Dependent Protein Kinases / metabolism
  • Humans
  • Leptin / genetics
  • Leptin / metabolism
  • Lipolysis* / genetics
  • Mice
  • Mutation
  • Obesity / genetics
  • Obesity / metabolism*
  • PPAR gamma* / genetics
  • PPAR gamma* / metabolism
  • Signal Transduction

Substances

  • Catecholamines
  • Leptin
  • PPAR gamma
  • Cyclic AMP-Dependent Protein Kinases