Glycosphingolipid storage in Fabry mice extends beyond globotriaosylceramide and is affected by ABCB1 depletion

نویسندگان

  • Mustafa A Kamani
  • Philippe Provençal
  • Michel Boutin
  • Natalia Pacienza
  • Xin Fan
  • Anton Novak
  • Tonny C Huang
  • Beth Binnington
  • Bryan C Au
  • Christiane Auray-Blais
  • Clifford A Lingwood
  • Jeffrey A Medin
چکیده

AIM Fabry disease is caused by α-galactosidase A deficiency leading to accumulation of globotriaosylceramide (Gb3) in tissues. Clinical manifestations do not appear to correlate with total Gb3 levels. Studies examining tissue distribution of specific acyl chain species of Gb3 and upstream glycosphingolipids are lacking. MATERIAL & METHODS/RESULTS Thorough characterization of the Fabry mouse sphingolipid profile by LC-MS revealed unique Gb3 acyl chain storage profiles. Storage extended beyond Gb3; all Fabry tissues also accumulated monohexosylceramides. Depletion of ABCB1 had a complex effect on glycosphingolipid storage. CONCLUSION These data provide insights into how specific sphingolipid species correlate with one another and how these correlations change in the α-galactosidase A-deficient state, potentially leading to the identification of more specific biomarkers of Fabry disease.

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عنوان ژورنال:

دوره 2  شماره 

صفحات  -

تاریخ انتشار 2016