Finkel-Biskis-Reilly osteosarcoma virus v-Fos inhibits adipogenesis and both the activity and expression of CCAAT/enhancer binding protein alpha, a key regulator of adipocyte differentiation

J Biol Chem. 1997 Dec 19;272(51):32454-62. doi: 10.1074/jbc.272.51.32454.

Abstract

Finkel-Biskis-Reilly (FBR) osteosarcoma virus v-Fos causes tumors of mesenchymal origin, including osteosarcomas, rhabdomyosarcomas, chondrosarcomas, and liposarcomas. Because the cell of origin in all these tumors is a pluripotent mesenchymal cell, the variety of tumors seen in mice which express FBR v-Fos implies that FBR v-Fos inhibits multiple differentiation pathways. To study the mechanism of FBR v-Fos' inhibition of mesenchymal differentiation, we utilized an in vitro model of adipocyte differentiation. We show by both morphological and biochemical means that FBR v-Fos inhibits adipocyte differentiation in vitro. This inhibition is due to FBR v-Fos' inhibition of the growth arrest characteristic of terminal differentiation and FBR v-Fos' inhibition of the expression and activity of a key regulator of this growth arrest, C/EBPalpha. The in vitro inhibition of adipogenesis by FBR v-Fos has in vivo significance as immunostaining of FBR v-Fos-induced tumors shows no CCAAT/enhancer binding protein (EBP)-alpha expression. These data implicate C/EBPalpha as a protein involved in the generation of liposarcomas.

Publication types

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

MeSH terms

  • 3T3 Cells
  • Adipose Tissue / cytology
  • Adipose Tissue / growth & development*
  • Animals
  • CCAAT-Enhancer-Binding Proteins
  • Cell Differentiation / genetics*
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / physiology
  • HeLa Cells
  • Humans
  • Mice
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / physiology
  • Oncogene Proteins v-fos / genetics
  • Oncogene Proteins v-fos / physiology*
  • Osteosarcoma / pathology
  • Osteosarcoma / virology*
  • Retroviridae / genetics*
  • Transcription, Genetic

Substances

  • CCAAT-Enhancer-Binding Proteins
  • DNA-Binding Proteins
  • Nuclear Proteins
  • Oncogene Proteins v-fos