Peroxisome proliferator‐activated receptor gamma‐coactivator‐1 alpha coordinates sphingolipid metabolism, lipid raft composition and myelin protein synthesis. Issue 5 (14th June 2013)

• Record Type: Journal Article
• Authors: Camacho, Alberto; Huang, Jeffrey K.; Delint‐Ramirez, Ilse; Yew Tan, Chong; Fuller, Maria; Lelliott, Christopher J.; Vidal‐Puig, Antonio; Franklin, Robin J. M.
• Is Part Of: European journal of neuroscience. Volume 38:Issue 5(2013:Sep.)
• Page Start: 2672
• Page End: 2683
• Publication Date: 2013-06-14
• Subjects: Nervous system -- Periodicals; 612.8
• DOI: 10.1111/ejn.12281
• Languages: English
• ISSNs: 0953-816X

Abstract

<abstract abstract-type="main" id="ejn12281-abs-0001"> <title>Abstract</title> <p>Peroxisome proliferator‐activated receptor gamma‐coactivator‐1 alpha (PGC1a) is involved in energy and lipid metabolism, and its loss leads to neurodegenerative changes in the striatum. Here we performed lipidomic analysis on brain extracts from PGC1a mutant and wild‐type mice. We found increased phosphatidylcholine and decreased ceramides in the brain of PGC1a‐deficient mice. An analysis of lipid raft fractions revealed increased ceramide, glucocylceramides and GM1 ganglioside in the PGC1a mutants. In the cerebellum, we observed a decrease in proteins associated with myelination, but were unable to detect any morphological abnormalities in compact myelin formation in PGC1a mutants compared with wild‐type mice. Although PGC1a is involved in lipid biosynthesis, we concluded that altered lipid composition in the PGC1a mutant did not directly affect central nervous system myelin morphology.</p> </abstract>