Elevated nucleocytoplasmic glycosylation by O-GlcNAc results in insulin resistance associated with defects in Akt activation in 3T3-L1 adipocytes

Proc Natl Acad Sci U S A. 2002 Apr 16;99(8):5313-8. doi: 10.1073/pnas.072072399.

Abstract

Increased flux of glucose through the hexosamine biosynthetic pathway (HSP) is believed to mediate hyperglycemia-induced insulin resistance in diabetes. The end product of the HSP, UDP beta-N-acetylglucosamine (GlcNAc), is a donor sugar nucleotide for complex glycosylation in the secretory pathway and for O-linked GlcNAc (O-GlcNAc) addition to nucleocytoplasmic proteins. Cycling of the O-GlcNAc posttranslational modification was blocked by pharmacological inhibition of O-GlcNAcase, the enzyme that catalyzes O-GlcNAc removal from proteins, with O-(2-acetamido-2-deoxy-d-glucopyranosylidene)amino-N-phenylcarbamate (PUGNAc). PUGNAc treatment increased levels of O-GlcNAc and caused insulin resistance in 3T3-L1 adipocytes. Insulin resistance induced through the HSP by glucosamine and chronic insulin treatment correlated with increased O-GlcNAc levels on nucleocytoplasmic proteins. Whereas insulin receptor autophosphorylation and insulin receptor substrate 2 tyrosine phosphorylation were not affected by PUGNAc inhibition of O-GlcNAcase, downstream phosphorylation of Akt at Thr-308 and glycogen synthase kinase 3 beta at Ser-9 was inhibited. PUGNAc-induced insulin resistance was associated with increased O-GlcNAc modification of several proteins including insulin receptor substrate 1 and beta-catenin, two important effectors of insulin signaling. These results suggest that elevation of O-GlcNAc levels attenuate insulin signaling and contribute to the mechanism by which increased flux through the HSP leads to insulin resistance in adipocytes.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • 3T3 Cells
  • Acetylglucosamine / analogs & derivatives*
  • Acetylglucosamine / metabolism*
  • Adipocytes / metabolism*
  • Animals
  • Blotting, Western
  • Calcium-Calmodulin-Dependent Protein Kinases / metabolism
  • Catalysis
  • Cell Line
  • Cell Nucleus / metabolism*
  • Cytoplasm / metabolism*
  • Cytoskeletal Proteins / metabolism
  • Dose-Response Relationship, Drug
  • Enzyme Activation
  • Glucosamine / metabolism
  • Glucose / pharmacokinetics
  • Glycogen Synthase Kinase 3
  • Glycogen Synthase Kinases
  • Glycosylation
  • Insulin / metabolism
  • Insulin / pharmacology
  • Insulin Receptor Substrate Proteins
  • Insulin Resistance*
  • Mice
  • Oximes / metabolism
  • Phenylcarbamates*
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Precipitin Tests
  • Protein Binding
  • Protein Processing, Post-Translational
  • Protein Serine-Threonine Kinases*
  • Proto-Oncogene Proteins / metabolism*
  • Proto-Oncogene Proteins c-akt
  • Signal Transduction
  • Time Factors
  • Trans-Activators*
  • Tyrosine / metabolism
  • beta Catenin

Substances

  • CTNNB1 protein, mouse
  • Cytoskeletal Proteins
  • Insulin
  • Insulin Receptor Substrate Proteins
  • Irs1 protein, mouse
  • Oximes
  • Phenylcarbamates
  • Phosphoproteins
  • Proto-Oncogene Proteins
  • Trans-Activators
  • beta Catenin
  • N-acetylglucosaminono-1,5-lactone O-(phenylcarbamoyl)oxime
  • Tyrosine
  • Glycogen Synthase Kinases
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt
  • Calcium-Calmodulin-Dependent Protein Kinases
  • Glycogen Synthase Kinase 3
  • Glucose
  • Glucosamine
  • Acetylglucosamine