Insulin signaling controls the expression of O-GlcNAc transferase and its interaction with lipid microdomains. FASEB J 2013 Sep;27(9):3478-86
Date
05/22/2013Pubmed ID
23689613DOI
10.1096/fj.12-217984Scopus ID
2-s2.0-84883416868 (requires institutional sign-in at Scopus site) 39 CitationsAbstract
Lipid microdomains (rafts) are cholesterol-enriched dynamic ordered lipid domains belonging to cell membranes involved in diverse cellular functions, including signal transduction, membrane trafficking, and infection. Many studies have reported relationships between insulin signaling and lipid rafts. Likewise, links between insulin signaling and O-GlcNAcylation have also been described. However, the potential connection between O-GlcNAc and raft dynamics remains unexplored. Here we show that O-GlcNAc and the enzyme that creates this modification, O-GlcNAc transferase (OGT), are localized in rafts. On insulin stimulation, we observe time-dependent increases in OGT expression and localization within rafts. We show that these processes depend on activation of the phosphatidylinositol 3-kinase (PI3K) pathway. Inhibition of OGT does not significantly affect cholesterol synthesis and raft building but decreases insulin receptor expression and PI3K and mitogen-activated protein kinase pathway activation. Taken together, these findings indicate that O-GlcNAcylation, lipid rafts, and signaling pathways are spatiotemporally coordinated to enable fundamental cellular functions.
Author List
Perez-Cervera Y, Dehennaut V, Aquino Gil M, Guedri K, Solórzano Mata CJ, Olivier-Van Stichelen S, Michalski JC, Foulquier F, Lefebvre TAuthor
Stephanie Olivier-Van Stichelen PhD Assistant Professor in the Biochemistry department at Medical College of WisconsinMESH terms used to index this publication - Major topics in bold
Blotting, WesternCholesterol
Hep G2 Cells
Humans
Insulin
Membrane Proteins
Microscopy, Fluorescence
N-Acetylglucosaminyltransferases
Phosphatidylinositol 3-Kinases
Receptor, Insulin
Signal Transduction
