Myelin and Lipid Composition of the Corpus Callosum in Mucopolysaccharidosis Type I Mice

Steven Q. Le, Igor Nestrasil, Shih hsin Kan, Martin Egeland, Jonathan D. Cooper, David Elashoff, Rong Guo, Jakub Tolar, Jennifer K. Yee, Patricia I. Dickson

Research output: Contribution to journalArticlepeer-review

3 Scopus citations

Abstract

Mucopolysaccharidosis type I (MPS I) is a lysosomal disease with progressive central nervous system involvement. This study examined the lipid, cholesterol, and myelin basic protein composition of white matter in the corpus callosum of MPS I mice. We studied 50 week-old, male MPS I mice and littermate, heterozygote controls (n = 12 per group). Male MPS I mice showed lower phosphatidylcholine and ether-linked phosphatidylcholine quantities than controls (p < 0.05). Twenty-two phospholipid or ceramide species showed significant differences in percent of total. Regarding specific lipid species, MPS I mice exhibited lower quantities of sphingomyelin 18:1, phosphatidylserine 38:3, and hexosylceramide d18:1(22:1) mH2O than controls. Principal components analyses of polar, ceramide, and hexosylceramide lipids, respectively, showed some separation of MPS I and control mice. We found no significant differences in myelin gene expression, myelin basic protein, or total cholesterol in the MPS I mice versus heterozygous controls. There was a trend toward lower proteolipid protein-1 levels in MPS I mice (p = 0.06). MPS I mice show subtle changes in white matter composition, with an unknown impact on pathogenesis in this model.

Original languageEnglish (US)
Pages (from-to)627-637
Number of pages11
JournalLipids
Volume55
Issue number6
DOIs
StatePublished - Nov 2020

Bibliographical note

Publisher Copyright:
© 2020 AOCS

Keywords

  • Glycosaminoglycans
  • Hurler syndrome
  • Inborn errors of metabolism
  • Lipidomics
  • Lysosomal storage disease

Fingerprint

Dive into the research topics of 'Myelin and Lipid Composition of the Corpus Callosum in Mucopolysaccharidosis Type I Mice'. Together they form a unique fingerprint.

Cite this