Modulation of adipocyte differentiation by tumor necrosis factor and transforming growth factor beta

J Cell Biol. 1989 Mar;108(3):1105-13. doi: 10.1083/jcb.108.3.1105.

Abstract

Cultured TA1 adipocytes treated with tumor necrosis factor alpha (TNF) lose intracytoplasmic lipid and, over a period of days, come to resemble their predifferentiated progenitors (preadipocytes). To examine the extent to which this phenotypic reversion represents a return to a less differentiated cell, we examined three major characteristics that distinguish preadipocytes from adipocytes: (a) pattern of gene expression; (b) hormonal requirement for accelerated adipogenesis; and (c) pattern of protein synthesis. We found that within hours of TNF addition to adipocytes, mRNAs for genes whose expression is augmented during adipogenesis decreased to predifferentiated levels; in addition, like preadipocytes, TNF-treated adipocytes required exposure to hormones to accelerate adipogenesis. Further, the pattern of protein synthesis seen on polyacrylamide gels reverted to that seen before differentiation. Transforming growth factor-beta (TGF-beta) also caused a rapid decrease in expression of adipose genes when added to fully differentiated cells, an effect that was achieved by treatment with either TGF-beta 1 or TGF-beta 2. These effects were seen in the absence of a demonstrable proliferative response to either TNF or TGF-beta. Thus characteristics that define the "terminally" differentiated state in adipocytes are subject to modulation by environmental influences.

Publication types

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

MeSH terms

  • Adipose Tissue / cytology*
  • Adipose Tissue / drug effects
  • Cell Differentiation / drug effects
  • Cell Line
  • Dexamethasone / pharmacology
  • Gene Expression Regulation / drug effects
  • Indomethacin / pharmacology
  • Protein Biosynthesis
  • RNA, Messenger / genetics
  • Recombinant Proteins / pharmacology
  • Transcription, Genetic / drug effects
  • Transforming Growth Factors / pharmacology*
  • Tumor Necrosis Factor-alpha / pharmacology*

Substances

  • RNA, Messenger
  • Recombinant Proteins
  • Tumor Necrosis Factor-alpha
  • Transforming Growth Factors
  • Dexamethasone
  • Indomethacin