Sphingosine-1-phosphate phosphohydrolase regulates endoplasmic reticulum-to-golgi trafficking of ceramide

Mol Cell Biol. 2006 Jul;26(13):5055-69. doi: 10.1128/MCB.02107-05.

Abstract

Previous studies demonstrated that sphingosine-1-phosphate (S1P) phosphohydrolase 1 (SPP-1), which is located mainly in the endoplasmic reticulum (ER), regulates sphingolipid metabolism and apoptosis (H. Le Stunff et al., J. Cell Biol. 158:1039-1049, 2002). We show here that the treatment of SPP-1-overexpressing cells with S1P, but not with dihydro-S1P, increased all ceramide species, particularly the long-chain ceramides. This was not due to inhibition of ceramide metabolism to sphingomyelin or monohexosylceramides but rather to the inhibition of ER-to-Golgi trafficking, determined with the fluorescent ceramide analog N-(4,4-difluoro-5,7-dimethyl-4-bora-3a,4a-diaza-s-indacene-3-pentanoyl)-d-erythro-sphingosine (DMB-Cer). Fumonisin B1, an inhibitor of ceramide synthase, prevented S1P-induced elevation of all ceramide species and corrected the defect in ER transport of DMB-Cer, readily allowing its detection in the Golgi. In contrast, ceramide accumulation had no effect on either the trafficking or the metabolism of 6-([N-(7-nitrobenzo-2-oxa-1,3-diazol-4-yl)amino]hexanoyl)-sphingosine, which rapidly labels the Golgi even at 4 degrees C. Protein trafficking from the ER to the Golgi, determined with vesicular stomatitis virus ts045 G protein fused to green fluorescent protein, was also inhibited in SPP-1-overexpressing cells in the presence of S1P but not in the presence of dihydro-S1P. Our results suggest that SPP-1 regulates ceramide levels in the ER and thus influences the anterograde membrane transport of both ceramide and proteins from the ER to the Golgi apparatus.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biological Transport / drug effects
  • Boron Compounds / analysis
  • Boron Compounds / metabolism
  • Cells, Cultured
  • Ceramides / analysis
  • Ceramides / metabolism*
  • Endoplasmic Reticulum / enzymology
  • Endoplasmic Reticulum / metabolism*
  • Fumonisins / pharmacology
  • Glucosyltransferases / antagonists & inhibitors
  • Glucosyltransferases / metabolism
  • Golgi Apparatus / enzymology
  • Golgi Apparatus / metabolism*
  • Green Fluorescent Proteins / analysis
  • Green Fluorescent Proteins / genetics
  • Humans
  • Lysophospholipids / pharmacology
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism
  • Membrane Proteins / genetics
  • Membrane Proteins / metabolism*
  • Oxidoreductases / antagonists & inhibitors
  • Phosphoric Monoester Hydrolases / genetics
  • Phosphoric Monoester Hydrolases / metabolism*
  • Protein Transport / drug effects
  • Sphingosine / analogs & derivatives
  • Sphingosine / pharmacology
  • Viral Envelope Proteins / genetics
  • Viral Envelope Proteins / metabolism

Substances

  • Boron Compounds
  • Ceramides
  • Fumonisins
  • G protein, vesicular stomatitis virus
  • Lysophospholipids
  • Membrane Glycoproteins
  • Membrane Proteins
  • N-(4,4-difluoro-5,7-dimethyl-4--bora-3a,4a-diaza-s-indacene-3-pentanoyl)sphingosine
  • Viral Envelope Proteins
  • Green Fluorescent Proteins
  • sphingosine 1-phosphate
  • fumonisin B1
  • Oxidoreductases
  • dihydroceramide desaturase
  • Glucosyltransferases
  • ceramide glucosyltransferase
  • sphingosine-1-phosphate phosphatase
  • Phosphoric Monoester Hydrolases
  • Sphingosine