FEBS Letters
Volume 584, Issue 3 , Pages 537-542, 5 February 2010

GLUT4 molecules are recruited at random for insertion within the plasma membrane upon insulin stimulation

Edited by Daniela Ruffell

  • Marion Berenguer
  • ,
  • Yannick Le Marchand-Brustel
  • ,
  • Roland Govers

      Affiliations

    • Corresponding Author InformationCorresponding author. Address: INSERM, U895, Mediterranean Research Centre for Molecular Medicine (C3M), Avenir Team 9, Bâtiment Archimed, 151 Route de Ginestière, BP 23194, 06204 Nice Cedex 3, France. Fax: +33 4 89064221.

INSERM, U895, Mediterranean Research Centre for Molecular Medicine (C3M), Avenir Team 9, Nice F-06204, France

University of Nice-Sophia-Antipolis, Faculty of Medicine, Signaling and Pathologies (IFR50), Nice F-06107, France

Received 15 September 2009; received in revised form 30 November 2009; accepted 30 November 2009. published online 07 December 2009.

Abstract 

Glucose transporter 4 (GLUT4) is efficiently retained intracellularly. Here, we investigated the insulin-induced reduction of retention. While increasing insulin concentrations led to gradual increases in both the amount of recycling GLUT4 molecules and cell surface GLUT4 levels, the kinetics of the increase in time was independent of insulin concentration. To determine whether there are GLUT4 subpools that have a distinct insulin sensitivity, adipocytes were consecutively stimulated twice with a low concentration of insulin while recycling GLUT4 molecules were continuously labeled. This revealed that not the same pool of GLUT4 molecules was mobilized twice and thus that upon insulin stimulation, GLUT4 is likely to be recruited at random for insertion within the plasma membrane.

Keywords: Glucose transporter type 4, Insulin-responsive glucose transporter, Protein translocation, Protein trafficking, Insulin

Abbreviations: BSA, bovine serum albumin, DMEM, Dulbecco’s modified Eagle’s medium, GLUT4, insulin-responsive glucose transporter 4, GSC, GLUT4 storage compartment, GSV, GLUT4 storage vesicle, HA, hemagglutinin

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0014-5793(09)01036-9

doi:10.1016/j.febslet.2009.11.093

FEBS Letters
Volume 584, Issue 3 , Pages 537-542, 5 February 2010