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Journal of Lipid Research, Vol. 49, 1725-1734, August 2008 Lipid composition of microdomains is altered in a cell model of Gaucher disease*
* Lysosomal Diseases Research Unit, Department of Genetic Medicine, Children, Youth and Women's Health Service, North Adelaide, South Australia 5006 * This work was supported by a National Health and Medical Research Council project grant in Australia. Published, JLR Papers in Press, April 21, 2008.
1 To whom correspondence should be addressed. e-mail: maria.fuller{at}adelaide.edu.au The formation of cholesterol and sphingolipids into specialized liquid-ordered membrane microdomains (rafts) has been proposed to function in the intracellular sorting and transport of proteins and lipids. Defined by biochemical criteria, rafts resist solubilization in nonionic detergents, enabling them to be isolated as detergent-resistant membranes (DRM). In this study, we characterized the lipid composition of DRM from a cell model of the sphingolipid storage disorder, Gaucher disease, in which the catabolism of the sphingolipid glucosylceramide (GC) is impaired. In this cell model, we showed that GC accumulated primarily in the DRM, with smaller secondary increases in ceramide, dihexosylceramide, trihexosylceramide, and phosphatidylglycerol. This suggested that not only was lipid metabolism altered as a consequence of the cells' inability to degrade GC, but this affected the DRM rather than other regions of the membrane. This increase in lipids in the DRM may be responsible for the altered lipid and protein sorting seen in Gaucher disease. Analysis of individual lipid species revealed preservation of the shorter and fully saturated fatty acid species in the DRM, suggesting that the highly ordered and tightly packed nature of the DRM is maintained.
Supplementary key words membrane rafts detergent-resistant membranes mass spectrometry glucosylceramide lysosomal storage disorder sphingolipids phospholipids Abbreviations: Cer, ceramide; DHC, dihexosylceramide; DRM, detergent-resistant membranes; ESI-MS/MS, electrospray ionization tandem mass spectrometry; GC, glucosylceramide; HRP, horseradish peroxidase; PC, phosphatidylcholine; PG, phosphatidylglycerol; PI, phosphatidylinositol; PVDF, polyvinylidene fluoride; SM, sphingomyelin; THC, trihexosylceramide
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