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Electroporated GLUT4-7myc-GFP detects in vivo glucose transporter 4 translocation in skeletal muscle without discernible changes in GFP patterns.

Jonas Roland Knudsen | Carlos Henriquez-Olguin | Zhencheng Li | Thomas Elbenhardt Jensen
Experimental physiology | 2019

What is the central question of this study? Resolving the mechanism(s) leading to glucose transporter 4 (GLUT4) translocation to the muscle surface membrane has great therapeutic potential. However, the measurement of GLUT4 translocation is technically challenging. Here, we asked whether electroporation of GLUT4-7myc-GFP into skeletal muscle could be used as a tool to study GLUT4 translocation in vivo. What is the main finding and its importance? By acutely inducing GLUT4-7myc-GFP expression in skeletal muscle, we verified that in vivo exercise and AICAR stimulation increased the GLUT4 presence in the sarcolemma measured as myc signal. Importantly, the increased myc signal in the sarcolemma was not accompanied by major visual changes in the distribution of the GFP signal.

Pubmed ID: 30710396

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Associated grants

  • Agency: Novo Nordisk Foundation (NNF) Excellence project grant, International
    Id: #15182
  • Agency: China Scholarship Council (CSC), International
  • Agency: Danish Diabetes Academy funded by the NNF, International

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