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Nuclear sphingomyelin-synthase and protein kinase C delta in melanoma cells.

Abstract
The aim of this research is to study the influence of protein kinase C delta on the nuclear phospholipids metabolism. Murine and human melanoma cells, in which overexpression of protein kinase delta was induced, were used. After purification of the nuclei, the phosphatidylcholine-dependent phospholipase C, sphingomyelin-synthase, and sphingomyelinase activities were measured. The results showed that the nuclear sphingomyelin-synthase activity increased and sphingomyelinase activity decreased in the protein kinase C delta overexpressive cells with respect to the controls. As a consequence, the ceramide pool decreased and diacylglycerol pool increased; this effect was not due to the phosphatidylcholine-dependent phospholipase C activity that did not change. The inhibition of sphingomyelinase could be due to protein kinase C delta as well as to existence of a sort of nuclear self-regulation between sphingomyelin-synthase and sphingomyelinase. The possible role of nuclear sphingomyelin-synthase in cell proliferation is discussed.
AuthorsElisabetta Albi, Caterina A M La Porta, Samuela Cataldi, Mariapia Viola Magni
JournalArchives of biochemistry and biophysics (Arch Biochem Biophys) Vol. 438 Issue 2 Pg. 156-61 (Jun 15 2005) ISSN: 0003-9861 [Print] United States
PMID15907783 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Ceramides
  • Phosphatidylcholines
  • Prkcd protein, mouse
  • PRKCD protein, human
  • Protein Kinase C
  • Protein Kinase C-delta
  • Transferases (Other Substituted Phosphate Groups)
  • phosphatidylcholine-ceramide phosphocholine transferase
  • Type C Phospholipases
  • Sphingomyelin Phosphodiesterase
Topics
  • Animals
  • Cell Line, Tumor
  • Cell Nucleus (enzymology, metabolism)
  • Cell Proliferation
  • Ceramides (metabolism)
  • Humans
  • Melanoma (enzymology, metabolism)
  • Mice
  • Phosphatidylcholines (metabolism)
  • Protein Kinase C (biosynthesis, metabolism, physiology)
  • Protein Kinase C-delta
  • Sphingomyelin Phosphodiesterase (metabolism)
  • Transfection
  • Transferases (Other Substituted Phosphate Groups) (biosynthesis, physiology)
  • Type C Phospholipases (metabolism)

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