Regulation of gene expression by insulin in adipose cells: opposite effects on adipsin and glycerophosphate dehydrogenase genes

Mol Cell Endocrinol. 1989 May;63(1-2):199-208. doi: 10.1016/0303-7207(89)90096-8.

Abstract

Insulin is known to play the role of a positive effector both in vitro on the adipose conversion process and in vivo on the fatty acid synthesis and esterification processes in adipose tissue. The effects of insulin on the expression of two genes activated during adipose conversion, glycerol-3-phosphate dehydrogenase (GPDH) and adipsin genes, have been investigated in 3T3 F442A adipose cells. Within a physiological range of concentrations, insulin exerts opposite effects on the levels of GPDH (EC50 approximately 0.2 nM) and adipsin (EC50 approximately 1 nM) mRNAs. Its negative effect on the abundance of adipsin mRNA involves primarily a rapid inhibition of the transcriptional rate (less than 2 h). Its positive effect on the abundance of GPDH mRNA is due to a stimulation of the transcriptional rate accompanied by a delayed stabilization of GPDH mRNA. In addition, insulin exerts a specific effect on the length of the poly(A) tract of the adipsin mRNA. These results show that a single mechanism for the regulation of adipose-related genes by insulin can be excluded but rather suggest a complex phenomenon in which various levels of regulation take place.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adipose Tissue / analysis
  • Adipose Tissue / cytology*
  • Adipose Tissue / metabolism
  • Animals
  • Cell Line
  • Cells, Cultured
  • Complement Factor D
  • Gene Expression Regulation / drug effects
  • Glycerolphosphate Dehydrogenase / analysis
  • Glycerolphosphate Dehydrogenase / genetics*
  • Glycerolphosphate Dehydrogenase / metabolism
  • Insulin / pharmacology*
  • RNA, Messenger / analysis
  • RNA, Messenger / drug effects
  • RNA, Messenger / genetics
  • Rats
  • Serine Endopeptidases / genetics*
  • Serine Endopeptidases / metabolism
  • Time Factors
  • Transcription, Genetic / drug effects

Substances

  • Insulin
  • RNA, Messenger
  • Glycerolphosphate Dehydrogenase
  • Serine Endopeptidases
  • Complement Factor D