Lysophosphatidic acid inhibits adipocyte differentiation via lysophosphatidic acid 1 receptor-dependent down-regulation of peroxisome proliferator-activated receptor gamma2

J Biol Chem. 2005 Apr 15;280(15):14656-62. doi: 10.1074/jbc.M412585200. Epub 2005 Feb 14.

Abstract

Lysophosphatidic acid (LPA) is a bioactive phospholipid acting via specific G protein-coupled receptors that is synthesized at the extracellular face of adipocytes by a secreted lysophospholipase D (autotaxin). Preadipocytes mainly express the LPA(1) receptor subtype, and LPA increases their proliferation. In monocytes and CV1 cells LPA was recently reported to bind and activate peroxisome proliferator-activated receptor gamma (PPARgamma), a transcription factor also known to play a pivotal role in adipogenesis. Here we show that, unlike the PPARgamma agonist rosiglitazone, LPA was unable to increase transcription of PPARgamma-sensitive genes (PEPCK and ALBP) in the mouse preadipose cell line 3T3F442A. In contrast, treatment with LPA decreased PPARgamma2 expression, impaired the response of PPARgamma-sensitive genes to rosiglitazone, reduced triglyceride accumulation, and reduced the expression of adipocyte mRNA markers. The anti-adipogenic activity of LPA was also observed in the human SGBS (Simpson-Golabi-Behmel syndrome) preadipocyte cell line, as well as in primary preadipocytes isolated from wild type mice. Conversely, the anti-adipogenic activity of LPA was not observed in primary preadipocytes from LPA(1) receptor knock-out mice, which, in parallel, exhibited a higher adiposity than wild type mice. In conclusion, LPA does not behave as a potent PPARgamma agonist in adipocytes but, conversely, inhibits PPARgamma expression and adipogenesis via LPA(1) receptor activation. The local production of LPA may exert a tonic inhibitory effect on the development of adipose tissue.

Publication types

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

MeSH terms

  • 3T3 Cells
  • Adipocytes / cytology*
  • Adipocytes / metabolism
  • Adipose Tissue / metabolism
  • Animals
  • Blotting, Western
  • Carrier Proteins / metabolism
  • Cell Differentiation
  • Cell Line
  • Cell Proliferation
  • Culture Media, Serum-Free / pharmacology
  • Down-Regulation*
  • Fatty Acid-Binding Proteins
  • Glucose-6-Phosphate Isomerase / metabolism
  • Glycoproteins / metabolism
  • Humans
  • Hypoglycemic Agents / pharmacology
  • Lysophospholipids / metabolism
  • Lysophospholipids / pharmacology*
  • Male
  • Mice
  • Mice, Knockout
  • Mice, Transgenic
  • Monocytes / cytology
  • Multienzyme Complexes / metabolism
  • Oligonucleotides / genetics
  • PPAR gamma / metabolism*
  • Phosphodiesterase I
  • Phosphoenolpyruvate Carboxykinase (GTP) / metabolism
  • Phosphoric Diester Hydrolases
  • Pyrophosphatases
  • RNA / metabolism
  • RNA, Messenger / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction
  • Rosiglitazone
  • Thiazolidinediones / pharmacology
  • Time Factors
  • Transcription, Genetic
  • Triglycerides / metabolism

Substances

  • Carrier Proteins
  • Culture Media, Serum-Free
  • Fatty Acid-Binding Proteins
  • Glycoproteins
  • Hypoglycemic Agents
  • Lysophospholipids
  • Multienzyme Complexes
  • Oligonucleotides
  • PPAR gamma
  • RNA, Messenger
  • Thiazolidinediones
  • Triglycerides
  • Rosiglitazone
  • RNA
  • Phosphoric Diester Hydrolases
  • Phosphodiesterase I
  • alkylglycerophosphoethanolamine phosphodiesterase
  • Pyrophosphatases
  • Phosphoenolpyruvate Carboxykinase (GTP)
  • Glucose-6-Phosphate Isomerase
  • lysophosphatidic acid