Regulation of HMG-CoA synthase and HMG-CoA reductase by insulin and epidermal growth factor in HaCaT keratinocytes

J Invest Dermatol. 2000 Jan;114(1):83-7. doi: 10.1046/j.1523-1747.2000.00822.x.

Abstract

Synthesis of cholesterol, via the isoprenoid/mevalonate pathway, is required for keratinocyte growth and differentiation, and maintenance of the stratum corneum lipid lamellae. 3-hydroxy-3-methylglutaryl coenzyme A synthase catalyzes the first step in isoprenoid/mevalonate synthesis and under some conditions controls the flux into the pathway. We have investigated whether selected growth factors and hormones could increase 3-hydroxy-3-methylglutaryl coenzyme A synthase mRNA in keratinocytes. Northern blotting was used to demonstrate that 10 microg per ml insulin and 0.1 microg per ml epidermal growth factor both increased steady-state levels of 3-hydroxy-3-methylglutaryl coenzyme A synthase mRNA by 2.5 and 6-fold, respectively. Epidermal growth factor and insulin also increased 3-hydroxy-3-methylglutaryl coenzyme A reductase enzyme activity. 3-hydroxy-3-methylglutaryl coenzyme A synthase promoter activity in a luciferase reporter construct was increased 2-fold by insulin and 2.9-fold by epidermal growth factor. When a mutation in the sterol regulatory element was introduced into the 3-hydroxy-3-methylglutaryl coenzyme A synthase promoter, activity was not increased by insulin, but was increased by epidermal growth factor. Mutation of an AP-1 site in the 3-hydroxy-3-methylglutaryl coenzyme A synthase promoter did not affect the increase in activity following treatment with insulin or epidermal growth factor. Therefore, 3-hydroxy-3-methylglutaryl coenzyme A synthase expression in keratinocytes is regulated by insulin and epidermal growth factor by different mechanisms. These results suggest a role for hormones and growth factors in the control of epidermal cholesterol synthesis.

MeSH terms

  • Binding Sites / physiology
  • Calcimycin / pharmacology
  • Cell Line
  • Epidermal Growth Factor / pharmacology*
  • Humans
  • Hydroxymethylglutaryl CoA Reductases / metabolism*
  • Hydroxymethylglutaryl-CoA Synthase / genetics
  • Hydroxymethylglutaryl-CoA Synthase / metabolism*
  • Insulin / pharmacology*
  • Ionophores / pharmacology
  • Keratinocytes / drug effects*
  • Keratinocytes / enzymology*
  • Promoter Regions, Genetic / drug effects
  • Promoter Regions, Genetic / physiology
  • RNA, Messenger / metabolism
  • Transcription Factor AP-1 / metabolism

Substances

  • Insulin
  • Ionophores
  • RNA, Messenger
  • Transcription Factor AP-1
  • Calcimycin
  • Epidermal Growth Factor
  • Hydroxymethylglutaryl CoA Reductases
  • Hydroxymethylglutaryl-CoA Synthase