EFR3 and phosphatidylinositol 4-kinase IIIα regulate insulin-stimulated glucose transport and GLUT4 dispersal in 3T3-L1 adipocytes

Biosci Rep. 2022 Jul 29;42(7):BSR20221181. doi: 10.1042/BSR20221181.

Abstract

Insulin stimulates glucose transport in muscle and adipocytes. This is achieved by regulated delivery of intracellular glucose transporter (GLUT4)-containing vesicles to the plasma membrane where they dock and fuse, resulting in increased cell surface GLUT4 levels. Recent work identified a potential further regulatory step, in which insulin increases the dispersal of GLUT4 in the plasma membrane away from the sites of vesicle fusion. EFR3 is a scaffold protein that facilitates localization of phosphatidylinositol 4-kinase type IIIα to the cell surface. Here we show that knockdown of EFR3 or phosphatidylinositol 4-kinase type IIIα impairs insulin-stimulated glucose transport in adipocytes. Using direct stochastic reconstruction microscopy, we also show that EFR3 knockdown impairs insulin stimulated GLUT4 dispersal in the plasma membrane. We propose that EFR3 plays a previously unidentified role in controlling insulin-stimulated glucose transport by facilitating dispersal of GLUT4 within the plasma membrane.

Keywords: GLUT4; adipocytes; glucose transport; insulin.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 1-Phosphatidylinositol 4-Kinase* / metabolism
  • 3T3-L1 Cells
  • Adipocytes / metabolism
  • Animals
  • Biological Transport
  • Cell Membrane / metabolism
  • Glucose / metabolism
  • Glucose Transport Proteins, Facilitative / metabolism
  • Glucose Transporter Type 4 / genetics
  • Glucose Transporter Type 4 / metabolism
  • Insulin* / metabolism
  • Insulin* / pharmacology
  • Mice

Substances

  • Glucose Transport Proteins, Facilitative
  • Glucose Transporter Type 4
  • Insulin
  • 1-Phosphatidylinositol 4-Kinase
  • Glucose