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Papers In Press, published online ahead of print May 1, 2008
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Journal of Lipid Research, Vol. 49, 1039-1047, May 2008
Copyright © 2008 by American Society for Biochemistry and Molecular Biology
-toxin




* Department of Microbiology, Faculty of Pharmaceutical Science, Tokushima Bunri University, Tokushima, Japan
School of Medicine, Fujita Health University, Toyoake, Aichi, Japan
Department of Chemistry of Functional Molecule, Faculty of Pharmaceutical Science, Tokushima Bunri University, Tokushima, Japan
The online version of this article (available at http://www.jlr.org) contains supplementary data in the form of three figures.
Published, JLR Papers in Press, February 8, 2008.
1 To whom correspondence should be addressed. e-mail: sakurai{at}ph.bunri-u.ac.jp
Clostridium perfringens
-toxin induces the hemolysis of sheep erythrocytes by activating the metabolism of sphingomyelin (SM) via a GTP binding protein in membranes.
-Toxin stimulated the formation of 15-N-nervonoyl sphingosine (C24:1-ceramide), which was identified by positive ion fast atom bombardment-MS and 1H-NMR spectroscopy. C24:1-ceramide stimulated the toxin-induced hemolysis of saponin-pretreated sheep erythrocytes and increased the production of sphingosine 1-phosphate (S1P) in the cells, but N-lignoceroyl sphingosine did not. These events elicited by the toxin in the presence of C24:1-ceramide were significantly attenuated by treatment with dihydrosphingosine, a sphingosine kinase inhibitor. TLC showed that the level of C24:1-ceramide was highest among the ceramides with an unsaturated bond in the fatty acyl chain in the detergent-resistant membranes (DRMs). The toxin specifically bound to DRMs rich in cholesterol, resulting in the hydrolysis of N-nervonoic sphingomyelin (C24:1-SM) in DRMs. Treatment of the cells with pertussis toxin (PT) inhibited the
-toxin-induced formation of C24:1-ceramide from C24:1-SM in DRMs and hemolysis, indicating that endogenous sphingomyelinase, which hydrolyzes C24:1-SM to C24:1-ceramide, is controlled by PT-sensitive GTP binding protein in membranes. These results show that the toxin-induced metabolism of C24:1-SM to S1P in DRMs plays an important role in the toxin-induced hemolysis of sheep erythrocytes.
Supplementary key words C24:1-sphingomyelin LC-MS/MS detergent-soluble fractions
Abbreviations: C16:0-ceramide, N-palmitoyl sphingosine (d18:1/16:0); C24:0-ceramide, N-lignoceroyl sphingosine (d18:1/24:0); C24:1-ceramide, 15-N-nervonoyl sphingosine (d18:1/24:1); C24:2-ceramide, 15,18-N-tetracosadienoyl sphingosine (d18:1/24:2); C24:1-SM, N-nervonoic sphingomyelin; DGK, 1,2-diacylglycerol kinase; DHS, dihydrosphingosine; DRM, detergent-resistant membrane; FAB, fast atom bombardment; MβCD, methyl-β-cyclodextrin; N-OE, N-oleoylethanolamine; PT, pertussis toxin; S1P, sphingosine 1-phosphate; SM, sphingomyelin; SMase, sphingomyelinase
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