Literature DB >> 9356011

Moving GLUT4: the biogenesis and trafficking of GLUT4 storage vesicles.

S Rea1, D E James.   

Abstract

The GLUT4 system in muscle and fat cells plays an important role in whole-body glucose homeostasis. Insulin stimulates the translocation of GLUT4 from an intracellular storage compartment to the cell surface. The nature of this compartment remains largely unknown. We review recent studies describing the biogenesis and molecular constituents of the GLUT4 storage compartment and conclude that it is segregated from the endosomal and biosynthetic pathways. Further, we present evidence to suggest that the GLUT4 storage compartment moves directly to the plasma membrane in response to insulin and, hence, is analogous to small synaptic vesicles in neurons. We propose that the GLUT4 storage compartment be referred to as GLUT4 storage vesicles or GSVs.

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Year:  1997        PMID: 9356011     DOI: 10.2337/diab.46.11.1667

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  68 in total

Review 1.  Signaling pathways in insulin action: molecular targets of insulin resistance.

Authors:  J E Pessin; A R Saltiel
Journal:  J Clin Invest       Date:  2000-07       Impact factor: 14.808

2.  Eicosanoids participate in the regulation of cardiac glucose transport by contribution to a rearrangement of actin cytoskeletal elements.

Authors:  O Dransfeld; I Rakatzi; S Sasson; A Gruzman; M Schmitt; D Häussinger; J Eckel
Journal:  Biochem J       Date:  2001-10-01       Impact factor: 3.857

3.  Expression of a prenylation-deficient Rab4 inhibits the GLUT4 translocation induced by active phosphatidylinositol 3-kinase and protein kinase B.

Authors:  M Cormont; N Gautier; K Ilc; Y le Marchand-Brustel
Journal:  Biochem J       Date:  2001-05-15       Impact factor: 3.857

Review 4.  The role of insulin resistance in the pathogenesis of Alzheimer's disease: implications for treatment.

Authors:  G Stennis Watson; Suzanne Craft
Journal:  CNS Drugs       Date:  2003       Impact factor: 5.749

5.  GLUT4, AMP kinase, but not the insulin receptor, are required for hepatoportal glucose sensor-stimulated muscle glucose utilization.

Authors:  Rémy Burcelin; Valerie Crivelli; Christophe Perrin; Anabela Da Costa; James Mu; Barbara B Kahn; Morris J Birnbaum; C Ronald Kahn; Peter Vollenweider; Bernard Thorens
Journal:  J Clin Invest       Date:  2003-05       Impact factor: 14.808

6.  Entry of newly synthesized GLUT4 into the insulin-responsive storage compartment is GGA dependent.

Authors:  Robert T Watson; Ahmir H Khan; Megumi Furukawa; June Chunqiu Hou; Lin Li; Makoto Kanzaki; Shuichi Okada; Konstantin V Kandror; Jeffrey E Pessin
Journal:  EMBO J       Date:  2004-04-29       Impact factor: 11.598

Review 7.  Fluidity of insulin action.

Authors:  Jeffrey S Elmendorf
Journal:  Mol Biotechnol       Date:  2004-06       Impact factor: 2.695

8.  Munc18c function is required for insulin-stimulated plasma membrane fusion of GLUT4 and insulin-responsive amino peptidase storage vesicles.

Authors:  D C Thurmond; M Kanzaki; A H Khan; J E Pessin
Journal:  Mol Cell Biol       Date:  2000-01       Impact factor: 4.272

9.  Cell cycle phase-specific surface expression of nerve growth factor receptors TrkA and p75(NTR).

Authors:  J L Urdiales; E Becker; M Andrieu; A Thomas; J Jullien; L A van Grunsven; S Menut; G I Evan; D Martín-Zanca; B B Rudkin
Journal:  J Neurosci       Date:  1998-09-01       Impact factor: 6.167

10.  Disruption of cortical actin in skeletal muscle demonstrates an essential role of the cytoskeleton in glucose transporter 4 translocation in insulin-sensitive tissues.

Authors:  Joseph T Brozinick; Eric D Hawkins; Andrew B Strawbridge; Jeffrey S Elmendorf
Journal:  J Biol Chem       Date:  2004-07-06       Impact factor: 5.157

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