Differential regulation of sphingomyelinase and ceramidase activities by growth factors and cytokines. Implications for cellular proliferation and differentiation

J Biol Chem. 1995 Oct 6;270(40):23305-9. doi: 10.1074/jbc.270.40.23305.

Abstract

Sphingosine is a product of sphingolipid metabolism that has been linked to a protein kinase C-independent mitogenic response. In previously published data, utilizing an in vitro model system for platelet-derived growth factor (PDGF)-induced vascular smooth muscle proliferation, we have demonstrated that sphingosine is increased at the expense of a concomitant decrease in ceramide formation, implicating an altered ceramidase activity. To explore mechanisms of growth factor-stimulated sphingosine formation, we have developed and investigated a cell-free model system assessing ceramidase activity. We now report that an alkaline, membrane-associated, ceramidase activity in the rat glomerular mesangial cell, a smooth muscle-like pericyte, is up-regulated by growth factors, apparently via a tyrosine kinase phosphorylation mechanism. PDGF also stimulated sphingomyelinase activity which generates sufficient substrate to drive the subsequent ceramidase reaction. Inflammatory cytokines, including interleukin-1, and tumor necrosis factor-alpha, stimulated sphingomyelinase but not ceramidase activity, a result consistent with the cellular accumulation of the ceramide, apoptidic, differentiating second messenger. Mitogenic vasoconstrictor peptides such as endothelin-1 stimulated neither sphingomyelinase nor ceramidase activities. An inhibitor of ceramidase activity, N-oleoylethanolamine, reduced PDGF- but not endothelin-1-stimulated proliferation. Thus, we conclude that, in mesangial cells, growth factors but not vasoconstrictor peptides or cytokines induce mitogenesis, in part, through ceramidase-mediated sphingosine formation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amidohydrolases / antagonists & inhibitors
  • Amidohydrolases / metabolism*
  • Animals
  • Cell Differentiation / drug effects
  • Cell Differentiation / physiology
  • Cell Division / drug effects
  • Cell Division / physiology
  • Cell-Free System
  • Ceramidases
  • Cytokines / pharmacology*
  • Endocannabinoids
  • Endothelins / pharmacology
  • Enzyme Inhibitors / pharmacology
  • Ethanolamines / pharmacology
  • Glomerular Mesangium / cytology
  • Glomerular Mesangium / drug effects
  • Glomerular Mesangium / metabolism
  • Growth Substances / pharmacology*
  • Oleic Acids
  • Phosphorylation
  • Platelet-Derived Growth Factor / pharmacology
  • Protein-Tyrosine Kinases / metabolism
  • Rats
  • Sphingomyelin Phosphodiesterase / metabolism*
  • Sphingosine / metabolism
  • Up-Regulation / drug effects
  • Vasoconstrictor Agents / pharmacology

Substances

  • Cytokines
  • Endocannabinoids
  • Endothelins
  • Enzyme Inhibitors
  • Ethanolamines
  • Growth Substances
  • Oleic Acids
  • Platelet-Derived Growth Factor
  • Vasoconstrictor Agents
  • N-oleoylethanolamine
  • Protein-Tyrosine Kinases
  • Sphingomyelin Phosphodiesterase
  • Amidohydrolases
  • Ceramidases
  • Sphingosine