Complexin-2 redistributes to the membrane of muscle cells in response to insulin and contributes to GLUT4 translocation

Biochem J. 2021 Jan 29;478(2):407-422. doi: 10.1042/BCJ20200542.

Abstract

Insulin stimulates glucose uptake in muscle cells by rapidly redistributing vesicles containing GLUT4 glucose transporters from intracellular compartments to the plasma membrane (PM). GLUT4 vesicle fusion requires the formation of SNARE complexes between vesicular VAMP and PM syntaxin4 and SNAP23. SNARE accessory proteins usually regulate vesicle fusion processes. Complexins aide in neuro-secretory vesicle-membrane fusion by stabilizing trans-SNARE complexes but their participation in GLUT4 vesicle fusion is unknown. We report that complexin-2 is expressed and homogeneously distributed in L6 rat skeletal muscle cells. Upon insulin stimulation, a cohort of complexin-2 redistributes to the PM. Complexin-2 knockdown markedly inhibited GLUT4 translocation without affecting proximal insulin signalling of Akt/PKB phosphorylation and actin fiber remodelling. Similarly, complexin-2 overexpression decreased maximal GLUT4 translocation suggesting that the concentration of complexin-2 is finely tuned to vesicle fusion. These findings reveal an insulin-dependent regulation of GLUT4 insertion into the PM involving complexin-2.

Keywords: GLUT4-translocation; SNARE complex; complexin; insulin action; skeletal muscle cells.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Vesicular Transport / genetics
  • Adaptor Proteins, Vesicular Transport / metabolism*
  • Animals
  • Cell Membrane / drug effects
  • Cell Membrane / metabolism
  • Cells, Cultured
  • Glucose Transporter Type 4 / genetics
  • Glucose Transporter Type 4 / metabolism*
  • Insulin / genetics
  • Insulin / metabolism
  • Insulin / pharmacology*
  • Muscle, Skeletal / cytology
  • Myoblasts / drug effects
  • Myoblasts / metabolism*
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Protein Transport / drug effects
  • Proto-Oncogene Proteins c-akt / metabolism
  • Rats
  • Signal Transduction
  • rac1 GTP-Binding Protein / metabolism

Substances

  • Adaptor Proteins, Vesicular Transport
  • Glucose Transporter Type 4
  • Insulin
  • Nerve Tissue Proteins
  • Slc2a4 protein, rat
  • complexin II
  • Proto-Oncogene Proteins c-akt
  • Rac1 protein, rat
  • rac1 GTP-Binding Protein