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Insulin stimulates fusion, but not tethering, of GLUT4 vesicles in skeletal muscle of HA-GLUT4-GFP transgenic mice

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Author

  • Vladimir A. Lizunov
  • Karin Stenkula
  • Ivonne Lisinski
  • Oksana Gavrilova
  • Dena R. Yver
  • Alexandra Chadt
  • Hadi Al-Hasani
  • Joshua Zimmerberg
  • Samuel W. Cushman

Summary, in English

Insulin stimulates fusion, but not tethering, of GLUT4 vesicles in skeletal muscle of HA-GLUT4-GFP transgenic mice. Am J Physiol Endocrinol Metab 302: E950-E960, 2012. First published January 31, 2012; doi:10.1152/ajpendo.00466.2011.-Insulin regulates glucose uptake into fat and muscle by modulating the subcellular distribution of GLUT4 between the cell surface and intracellular compartments. However, quantification of these translocation processes in muscle by classical subcellular fractionation techniques is confounded by contaminating microfibrillar protein; dynamic studies at the molecular level are almost impossible. In this study, we introduce a muscle-specific transgenic mouse model in which HA-GLUT4-GFP is expressed under the control of the MCK promoter. HA-GLUT4-GFP was found to translocate to the plasma membrane and T-tubules after insulin stimulation, thus mimicking endogenous GLUT4. To investigate the dynamics of GLUT4 trafficking in skeletal muscle, we quantified vesicles containing HA-GLUT4-GFP near the sarcolemma and T-tubules and analyzed insulin-stimulated exocytosis at the single vesicle level by total internal reflection fluorescence and confocal microscopy. We found that only 10% of the intracellular GLUT4 pool comprised mobile vesicles, whereas most of the GLUT4 structures remained stationary or tethered at the sarcolemma or T-tubules. In fact, most of the insulin-stimulated exocytosis emanated from pretethered vesicles, whereas the small pool of mobile GLUT4 vesicles was not significantly affected by insulin. Our data strongly suggest that the mobile pool of GLUT4 vesicles is not a major site of insulin action but rather locally distributed. Most likely, pretethered GLUT4 structures are responsible for the initial phase of insulin-stimulated exocytosis.

Department/s

Publishing year

2012

Language

English

Pages

950-960

Publication/Series

American Journal of Physiology: Endocrinology and Metabolism

Volume

302

Issue

8

Document type

Journal article

Publisher

American Physiological Society

Topic

  • Physiology

Keywords

  • hemagglutinin
  • glucose transporter 4
  • green fluorescent protein
  • insulin
  • fusion

Status

Published

Research group

  • Medical Protein Science

ISBN/ISSN/Other

  • ISSN: 1522-1555