Salazard B, Bellon L, Jean S, Maraninchi M, El-Yazidi C, Orsière T, Margotat A, Botta A, Bergé-Lefranc J-L
Laboratoire de Biogénotoxicologie et Mutagenèse Environnementale, (EA 1784, IFR112, PMSE), Faculté de Médecine, Marseille, France.
Cell Biol Toxicol. 2004 Nov;20(6):375-85. doi: 10.1007/s10565-004-1471-1.
In this study we analyzed gene expression in 3T3-F442A pre-adipocyte cells that differentiate in the presence of micro-molar arsenate concentration. Two concentrations of arsenite (As2O3, 0.25 micromol/L and 0.5 micromol/L) were applied for three days with and without insulin (170 nmol/L) and gene expressions were evaluated by quantitative RT-PCR. The genes included genes of oxidative-stress responses: heme-oxygenase-1 (HO1) and the hypoxia inducible factor 1a (HIF1alpha), genes of cell-cycle: c-jun and Kruppel like factor 5 (KLF5), and genes that play important roles in adipose determination: a peroxisome proliferator-activated receptor (PPARgamma) and a CCAAT/ enhancer binding protein (C/EBPalpha). Arsenite induced the expression of HO1, HIF1alpha, KLF5, PPARgamma and C/EBPalpha. These results suggest that under condition of oxidative stress arsenite induces genes that are required for adipose differentiation.