Co-treatment with dexamethasone and octanoate induces adipogenesis in 3T3-L1 cells

Cell Biol Int. 2004;28(3):209-16. doi: 10.1016/j.cellbi.2003.11.020.

Abstract

We report here that octanoate, a medium chain fatty acid, induces adipocyte differentiation in 3T3-L1 cells by co-treatment with dexamethasone, although octanoate has been known not to stimulate 3T3-L1 adipogenesis. A low concentration of exogenous glucose prevented 3T3-L1 adipogenesis induced by 1-methyl 3-isobutylxanthine, dexamethasone, and insulin (MDI) treatment (a common protocol for adipocyte differentiation). In contrast, co-treatment with dexamethasone and octanoate (D-OCT) induced adipogenesis under the same conditions. These findings imply that octanoate, rather than glucose, is the source of accumulated lipids in D-OCT-induced adipogenesis. D-OCT increased expression of the differentiation markers peroxisome proliferator-activated receptor (PPAR)gamma2 and caveolin-1. A specific inhibitor of p38 mitogen-activated protein (MAP) kinase inhibited D-OCT-induced adipogenesis. These results suggest that the p38 MAP kinase pathway followed by up-regulation of PPARgamma2 may be involved in 3T3-L1 adipocyte differentiation induced by D-OCT, as well as by MDI.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 3T3-L1 Cells
  • Adipose Tissue / drug effects*
  • Adipose Tissue / metabolism
  • Animals
  • Caprylates / pharmacology*
  • Caveolin 1
  • Caveolins / metabolism
  • Cell Differentiation / drug effects*
  • Cell Differentiation / physiology
  • Dexamethasone / pharmacology*
  • Glucocorticoids / pharmacology*
  • Glucose / metabolism
  • Imidazoles / pharmacology
  • Mice
  • Mitogen-Activated Protein Kinases / antagonists & inhibitors
  • Mitogen-Activated Protein Kinases / metabolism
  • Pyridines / pharmacology
  • Receptors, Cytoplasmic and Nuclear / metabolism
  • Transcription Factors / metabolism
  • Up-Regulation
  • p38 Mitogen-Activated Protein Kinases

Substances

  • Caprylates
  • Cav1 protein, mouse
  • Caveolin 1
  • Caveolins
  • Glucocorticoids
  • Imidazoles
  • Pyridines
  • Receptors, Cytoplasmic and Nuclear
  • Transcription Factors
  • Dexamethasone
  • Mitogen-Activated Protein Kinases
  • p38 Mitogen-Activated Protein Kinases
  • Glucose
  • octanoic acid
  • SB 203580