Insulin action on glucose transporters through molecular switches, tracks and tethers
Top Cited Papers
- 26 June 2008
- journal article
- review article
- Published by Portland Press Ltd. in Biochemical Journal
- Vol. 413 (2) , 201-215
- https://doi.org/10.1042/bj20080723
Abstract
Glucose entry into muscle cells is precisely regulated by insulin, through recruitment of GLUT4 (glucose transporter-4) to the membrane of muscle and fat cells. Work done over more than two decades has contributed to mapping the insulin signalling and GLUT4 vesicle trafficking events underpinning this response. In spite of this intensive scientific research, there are outstanding questions that continue to challenge us today. The present review summarizes the knowledge in the field, with emphasis on the latest breakthroughs in insulin signalling at the level of AS160 (Akt substrate of 160 kDa), TBC1D1 (tre-2/USP6, BUB2, cdc16 domain family member 1) and their target Rab proteins; in vesicle trafficking at the level of vesicle mobilization, tethering, docking and fusion with the membrane; and in the participation of the cytoskeleton to achieve optimal temporal and spatial location of insulin-derived signals and GLUT4 vesicles.Keywords
This publication has 183 references indexed in Scilit:
- Direct Quantification of Fusion Rate Reveals a Distal Role for AS160 in Insulin-stimulated Fusion of GLUT4 Storage VesiclesJournal of Biological Chemistry, 2008
- Mapping of R-SNARE function at distinct intracellular GLUT4 trafficking steps in adipocytesThe Journal of cell biology, 2008
- Regulation of multisite phosphorylation and 14-3-3 binding of AS160 in response to IGF-1, EGF, PMA and AICARBiochemical Journal, 2007
- Ins (endocytosis) and outs (exocytosis) of GLUT4 traffickingCurrent Opinion in Cell Biology, 2007
- ArPIKfyve–PIKfyve interaction and role in insulin-regulated GLUT4 translocation and glucose transport in 3T3-L1 adipocytesExperimental Cell Research, 2007
- AKT/PKB Signaling: Navigating DownstreamCell, 2007
- Substrate specificity and effect on GLUT4 translocation of the Rab GTPase-activating protein Tbc1d1Biochemical Journal, 2007
- The Glucose Transporter 4-regulating Protein TUG Is Essential for Highly Insulin-responsive Glucose Uptake in 3T3-L1 AdipocytesJournal of Biological Chemistry, 2007
- GLUT4 is internalized by a cholesterol-dependent nystatin-sensitive mechanism inhibited by insulinThe EMBO Journal, 2006
- SNAREs — engines for membrane fusionNature Reviews Molecular Cell Biology, 2006