Glucose transporter 4 can be inserted in the membrane without exposing its catalytic site for photolabeling from the medium

Science in China, Series C: Life Sciences

Volumn 50, Issue 2, 2007, Pages 147-154

  Niu, WenYan ^a   Ishiki, Manabu ^b   Bilan, Philip J ^b   Yao, Zhi ^a  

^a TIANJIN MEDICAL UNIVERSITY   (China)

^b HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

Glucose transport 4 (GLUT4); Insulin; Phosphatidylinositol 3,4,5 trisphosphate (PI(3,4,5)P3); Photolabel

Indexed keywords

GLUCOSE TRANSPORTER 4; INSULIN; PEPTIDE FRAGMENT; PHOSPHATIDYLINOSITOL; PHOSPHOINOSITIDE 3,4,5 TRIPHOSPHATE; PHOSPHOINOSITIDE-3,4,5-TRIPHOSPHATE; UNCLASSIFIED DRUG;

AMINO ACID SEQUENCE; ANIMAL; ARTICLE; BIOTINYLATION; CELL MEMBRANE; CELL STRAIN 3T3; CHEMISTRY; ENZYME ACTIVE SITE; L CELL; METABOLISM; MOUSE; RAT; SKELETAL MUSCLE;

3T3 CELLS; AMINO ACID SEQUENCE; ANIMALS; BIOTINYLATION; CATALYTIC DOMAIN; CELL MEMBRANE; GLUCOSE TRANSPORTER TYPE 4; INSULIN; L CELLS (CELL LINE); MICE; MUSCLE, SKELETAL; PEPTIDE FRAGMENTS; PHOSPHATIDYLINOSITOLS; RATS;

EID: 34247370118     PISSN: 10069305     EISSN: 18622798     Source Type: Journal    
DOI: 10.1007/s11427-007-0026-0     Document Type: Article

References (22)

1. Sweeney G, Garg R R, Ceddia R B, et al. Intracellular delivery of phosphatidylinositol (3,4,5)-trisphosphate causes incorporation of glucose transporter 4 into the plasma membrane of muscle and fat cells without increasing glucose uptake. J Biol Chem, 2004, 279(31): 32233-32242
2. Ishiki M, Randhawa V K, Poon V, et al. Insulin regulates the membrane arrival, fusion, and C-terminal unmasking of glucose transporter-4 via distinct phosphoinositides. J Biol Chem, 2005, 280(31): 28792-28802
3. Kanai F, Nishioka Y, Hayashi H, et al. Direct demonstration of insulin-induced GLUT4 translocation to the surface of intact cells by insertion of a c-myc epitope into an exofacial GLUT4 domain. J Biol Chem, 1993, 268(19): 14523-14526
4. Sweeney G, Somwar R, Ramlal T, et al. An inhibitor of p38 mitogen-activated protein kinase prevents insulin-stimulated glucose transport but not glucose transporter translocation in 3T3-L1 adipocytes and L6 myotubes. J Biol Chem, 1999, 274(15): 10071-10078
5. Robinson L J, Pang S, Harris D S, et al. Translocation of the glucose transporter (GLUT4) to the cell surface in permeabilized 3T3-L1 adipocytes: Effects of ATP insulin, and GTP gamma S and localization of GLUT4 to clathrin lattices. J Cell Biol, 1992, 117(6): 1181-1196
6. He T C, Zhou S, da Costa L T, et al. A simplified system for generating recombinant adenoviruses. Proc Natl Acad Sci USA, 1998, 95(5): 2509-2514
7. Koumanov F, Yang J, Jones A E, et al. Cell-surface biotinylation of GLUT4 using bis-mannose photolabels. Biochem J, 1998, 330 (Pt 3): 1209-1215
8. Holman G D, Kozka I J, Clark A E, et al. Cell surface labeling of glucose transporter isoform GLUT4 by bis-mannose photolabel. Correlation with stimulation of glucose transport in rat adipose cells by insulin and phorbol ester. J Biol Chem, 1990, 265: 18172-18179
9. Calrk A E, Holman G D. Exofacial photolabelling of the human erythrocyte glucose transporter with an azitrifluoroethylbenzoyl-substituted bismannose. Biochem J, 1990, 269(3): 615-622
10. Somwar R, Koterski S, Sweeney G, et al. A dominant-negative p38 MAPK mutant and novel selective inhibitors of p38 MAPK reduce insulin-stimulated glucose uptake in 3T3-L1 adipocytes without affecting GLUT4 translocation. J Biol Chem, 2002, 277(52): 50386-50395
11. Hansen P A, Wang W, Marshall B, et al. Dissociation of GLUT4 translocation and insulin-stimulated glucose transport in transgenic mice overexpressing GLUT1 in skeletal muscle. J Biol Chem, 1998, 273(29): 18173-18179
12. Clark A E, Holman G D, Kozka I J. Determination of the rates of appearance and loss of glucose transporters at the cell surface of rat adipose cells. Biochem J, 1991, 278(Pt 1): 235-241
13. Hausdorff S F, Fingar D C, Morioka K, et al. Identification of wort-mannin-sensitive targets in 3T3-L1 adipocytes. Dissociation of insulin-stimulated glucose uptake and glut4 translocation. J Biol Chem, 1999, 274(35): 24677-24684
14. Somwar R, Kim D Y, Sweeney G, et al. GLUT4 translocation precedes the stimulation of glucose uptake by insulin in muscle cells: Potential activation of GLUT4 via p38 mitogen-activated protein kinase. Biochem J, 2001, 359(Pt 3): 639-649
15. Maffucci T, Brancaccio A, Piccolo E, et al. Insulin induces phosphatidylinositol-3-phosphate formation through TC10 activation. EMBO J, 2003, 22(16): 4178-4189
16. Furtado L M, Somwar R, Sweeney G, et al. Activation of the glucose transporter GLUT4 by insulin. Biochem Cell Biol, 2002, 80(5): 569-578
17. Rudich A, Konrad D, Torok D, et al. Indinavir uncovers different contributions of GLUT4 and GLUT1 towards glucose uptake in muscle and fat cells and tissues. Diabetologia, 2003, 46(5): 649-658
18. Zierath J R, He L, Guma A, et al. Insulin action on glucose transport and plasma membrane GLUT4 content in skeletal muscle from patients with NIDDM. Diabetologia, 1996, 39(10): 1180-1189
19. Zierath J R, Krook A, Wallberg-Henriksson H. Insulin action in skeletal muscle from patients with NIDDM. Mol Cell Biochem, 1998, 182(1-2): 153-160
20. Hellwig B, Joost H G. Differentiation of erythrocyte-(GLUT1), liver-(GLUT2), and adipocyte-type (GLUT4) glucose transporters by binding of the inhibitory ligands cytochalasin B, forskolin, dipyridamole, and isobutylmethylxanthine. Mol Pharmacol, 1991, 40(3): 383-389
21. Klip A, Ramlal T, Douen A G, et al. Inhibition by forskolin of insulin-stimulated glucose transport in L6 muscle cells. Biochem J, 1988, 255(3): 1023-1029
22. Foster L J, Rudich A, Talior I, et al. Insulin-dependent interactions of proteins with GLUT4 revealed through stable isotope labeling by amino acid in cell culture (SILAC). J Proteome Res, 2006, 5(1): 64-75