Neutral sphingomyelinase action stimulates signal transduction of tumor necrosis factor-α in the synthesis of cholesteryl esters in human fibroblasts

Research output: Contribution to journalArticle

Abstract

We have investigated biochemical mechanisms of tumor necrosis factor (TNF)-α signaling in cultured human skin fibroblasts. We found that TNF-α signaling may involve activation of a cell membrane neutral sphingomyelinase (N-SMase) in that within 2.5-5 min of treatment of cells with TNF-α there was a 2-fold increase in the activity of N-SMase compared to control. This reaction led to the hydrolysis of sphingomyelin as evidenced by a decrease in sphingomyelin mass and in the radioactivity associated with [14C]choline- labeled sphingomyelin. This was accompanied by a 4-fold increase in the formation of cholesteryl [14C]oleate within 2.5 min of incubation with TNF- α. This reaction also stimulated the mobilization of cell surface-associated [3H]cholesterol and its utilization in the synthesis of [3H]cholesteryl esters via acyl coenzyme-A cholesterol acyltransferase (ACAT). Gas chromatographic analysis revealed that the cellular level of cholesteryl esters increased about 2.5-3-fold following treatment with TNF-α compared to control. Cholesteryl ester synthesis was compromised upon incubation of cells with antibody against N-SMase and remained unaltered with TNF-β and fibroblast growth factor. Furthermore, TNF-α-mediated stimulation of cholesteryl ester synthesis was compromised by incubation of cells with an inhibitor of ACAT. These findings suggest a possible biological role of N- SMase in the signal transduction of TNF-α in the synthesis of cholesteryl esters in human fibroblasts.

Original languageEnglish (US)
Pages (from-to)879-882
Number of pages4
JournalJournal of Biological Chemistry
Volume269
Issue number2
StatePublished - Jan 14 1994

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Biology
  • Cell Biology

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