Mapping insulin/GLUT4 circuitry

Traffic. 2011 Jun;12(6):672-81. doi: 10.1111/j.1600-0854.2011.01178.x. Epub 2011 Mar 15.


One of the most important metabolic actions of insulin is catalysing glucose uptake into skeletal muscle and adipose tissue. This is accomplished via activation of the phosphatidylinositol-3-kinase/Akt signalling pathway and subsequent translocation of GLUT4 from intracellular storage vesicles to the plasma membrane. As such, this represents an ideal system for studying the convergence of signal transduction and protein trafficking. The GLUT4 translocation process is complex, but can be dissected into at least four discrete trafficking steps. This raises the question as to which of these is the major regulated step in insulin-stimulated GLUT4 translocation. Numerous molecules have been reported to regulate GLUT4 trafficking. However, with the exception of TBC1D4, the molecular details of these distal signalling arms of the insulin signalling network and how they modify distinct steps of GLUT4 trafficking have not been established. We discuss the need to adopt a more global approach to expand and deepen our understanding of the molecular processes underpinning this system. Strategies that facilitate the generation of detailed models of the entire insulin signalling network will enable us to identify the critical nodes that control GLUT4 traffic and decipher emergent properties of the system that are not currently apparent.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adipose Tissue / metabolism
  • Animals
  • Cell Membrane / metabolism
  • Endocytosis / physiology
  • Enzyme Activation
  • Glucose / metabolism
  • Glucose Transporter Type 4 / metabolism*
  • Insulin / metabolism*
  • Isoenzymes / metabolism
  • Membrane Fusion
  • Muscle, Skeletal / metabolism
  • Protein Transport / physiology
  • Proteomics
  • Proto-Oncogene Proteins c-akt / metabolism
  • Signal Transduction / physiology*


  • Glucose Transporter Type 4
  • Insulin
  • Isoenzymes
  • Proto-Oncogene Proteins c-akt
  • Glucose