Regulation of glucose-transporter gene expression by insulin in cultured human fibroblasts

Diabetes. 1988 Nov;37(11):1583-6. doi: 10.2337/diab.37.11.1583.

Abstract

To clarify the effect of insulin on glucose-transporter (GT) biosynthesis, we determined GT mRNA levels in human cultured skin fibroblasts, using HepG2 GT cDNA as a probe. Insulin specifically increased the GT mRNA level in a time- and dose-dependent manner. Time-course study demonstrated that the mRNA level peaked within 3 h of insulin (1 x 10(-7) M) addition. After remaining elevated for several hours, mRNA decreased and returned to the basal level after 24 h. In the cell strains from seven normal subjects, the mean (+/- SE) GT mRNA level determined after 3 h of treatment with 1 x 10(-7) M insulin was 164.3 +/- 8.5% of the level found in untreated control cells. The insulin dose-response curve of GT mRNA levels showed that the maximum stimulation was elicited at 1 x 10(-7) M, and the half-maximum stimulation occurred at approximately 5 x 10(-10) M. Degradation rates of GT mRNA determined in the presence of actinomycin D were not different between insulin-treated and untreated cells. These results suggest that insulin increases GT gene expression in cultured human fibroblasts.

MeSH terms

  • Cells, Cultured
  • DNA / genetics
  • Dactinomycin / pharmacology
  • Fibroblasts / metabolism*
  • Gene Expression Regulation / drug effects*
  • Humans
  • Insulin / pharmacology*
  • Kinetics
  • Monosaccharide Transport Proteins / genetics*
  • Nucleic Acid Hybridization
  • RNA, Messenger / biosynthesis

Substances

  • Insulin
  • Monosaccharide Transport Proteins
  • RNA, Messenger
  • Dactinomycin
  • DNA