bioRxivCell Biology
EFR3 and phosphatidylinositol 4-kinase IIIα regulate insulin-stimulated glucose transport and GLUT4 dispersal in 3T3-L1 adipocytes.
A. M. Koester, K. M. Laidlaw, S. Morris, M. F. A. Cutiongco, L. Stirrat, N. Gadegaard, E. Boles, H. L. Black, N. Bryant, G. W. Gould
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 localisation of phosphatidylinositol 4-kinase type III to the cell surface. Here we show that knockdown of EFR3 or phosphatidylinositol 4-kinase type III 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.
- organism: mouse
- assay: proteomics
- research focus: cell signaling & trafficking
- approach: experimental assay
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