Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/124014
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Type: Journal article
Title: Glycosphingolipid analysis in a naturally occurring ovine model of acute neuronopathic Gaucher disease
Author: Karageorgos, L.
Hein, L.
Rozaklis, T.
Adams, M.
Duplock, S.
Snel, M.
Hemsley, K.
Kuchel, T.
Smith, N.
Hopwood, J.
Citation: Neurobiology of Disease, 2016; 91:143-154
Publisher: Elsevier
Issue Date: 2016
ISSN: 0969-9961
1095-953X
Statement of
Responsibility: 
Litsa Karageorgos, Leanne Hein, Tina Rozaklis, Melissa Adams, Stephen Duplock, Marten Snel, Kim Hemsley, Tim Kuchel, Nicholas Smith, John J. Hopwood
Abstract: Gaucher disease arises from mutations in the β-glucocerebrosidase gene which encodes an enzyme required for the lysosomal catabolism of glucosylceramide. We have identified a naturally occurring mutation in the β-glucocerebrosidase gene in sheep that leads to Gaucher disease with acute neurological symptoms. Here we have examined the clinical phenotype at birth and subsequently quantified lipids in Gaucher lamb brain, in order to characterise the disorder. Enzyme activity assessments showed that a reduction in β-glucocerebrosidase activity to 1-5% of wild-type occurs consistently across newborn Gaucher lamb brain regions. We analyzed glucosylceramide, glucosylsphingosine, bis(monoacylglycero)phosphate and ganglioside profiles in brain, liver, and spleen, and observed 30- to 130-fold higher glucosylceramide, and 500- to 2000-fold higher glucosylsphingosine concentrations in Gaucher diseased lambs compared to wild-type. Significant increases of bis(monoacylglycero)phosphate and gangliosides [GM1, GM2, GM3] concentrations were also detected in the brain. As these glycosphingolipids are involved in many cellular events, an imbalance or disruption of the cell membrane lipid homeostasis would be expected to impair normal neuronal function. To our knowledge, this is the first detailed analysis of glycosphingolipids in various brain regions in a large animal model of neuronal disease, which permits the mechanistic investigation of lipid deregulation and their contribution to neurodegenerative process.
Keywords: Glucocerebrosidase; Glucosylceramide; Lipid metabolism; Sheep model; Gangliosides; Sphingolipids
Description: Available online 11 March 2016
Rights: © 2016 Elsevier Inc. All rights reserved.
RMID: 0030046108
DOI: 10.1016/j.nbd.2016.03.011
Appears in Collections:Medicine publications

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