GLUT4
Glucose transporter type 4, also known as GLUT4, is a protein encoded, in humans, by the GLUT4 gene. GLUT4 is the insulin-regulated glucose transporter found primarily in adipose tissues and striated muscle (skeletal and cardiac). The first evidence for this distinct glucose transport protein was provided by David James in 1988.[1] The gene that encodes GLUT4 was cloned[2][3] and mapped in 1989.[4]
Recent reports demonstrated the presence of GLUT4 gene in central nervous system such as the hippocampus. Moreover, impairment in insulin-stimulated trafficking of GLUT4 in the hippocampus result in decreased metabolic activities and plasticity of hippocampal neurons, which leads to depressive like behaviour and cognitive dysfunction.[5][6][7]
Tissue distribution
GLUT4 is primarily found in:
Regulation
Insulin
Under conditions of low insulin, most GLUT4 is sequestered in intracellular vesicles in muscle and fat cells. Insulin induces a rapid increase in the uptake of glucose by inducing the translocation of GLUT4 from these vesicles to the plasma membrane. As the vesicles fuse with the plasma membrane, GLUT4 transporters are inserted and become available for transporting glucose, and glucose absorption increases.[8] Insulin’s actions are effectively abolished in the genetically engineered muscle insulin receptor knock‐out (MIRKO) mouse because they have a complete lack of the insulin‐sensitive glucose transport protein, GLUT4, in muscle, so insulin has no effect on glucose uptake. Fascinatingly, this is of little or no consequence to the animal that does not have fasting hyperglycaemia or diabetes.[9]
Insulin binds to the insulin receptor in its dimeric form and activates the receptor's tyrosine-kinase domain. The receptor then phosphorylates and subsequently recruits Insulin Receptor Substrate or IRS-1, which in turn binds the enzyme PI-3 kinase through the binding of the enzyme's SH2 domain to the pTyr of IRS. PI-3 kinase converts the membrane lipid PIP2 to PIP3. PIP3 is specifically recognized by the PH domains of PKB (protein kinase B)or AKT, and also for PDK1 which, being localized together with PKB, can phosphorylate and activate PKB. Once phosphorylated, PKB is in its active form and phosphorylates TBC1D4, which inhibits the GAP domain or the GTPase-activating domain associated with TBC1D4, allowing for Rab protein to change from its GDP to GTP bound state. Inhibition of the GTPase-activating domain leaves proteins next in the cascade in their active form and stimulates GLUT4 to be expressed on the plasma membrane. RAC1 is a GTPase which is also activated by insulin. Rac1 stimulates reorganization of the cortical Actin cytoskeleton [10] which allows for the GLUT4 vesicles to be inserted into the plasma membrane.[11][12] RAC1 Knockout mouse have reduced glucose uptake in muscle.[12]
At the cell surface, GLUT4 permits the facilitated diffusion of circulating glucose down its concentration gradient into muscle and fat cells. Once within cells, glucose is rapidly phosphorylated by glucokinase in the liver and hexokinase in other tissues to form glucose-6-phosphate, which then enters glycolysis or is polymerized into glycogen. Glucose-6-phosphate cannot diffuse back out of cells, which also serves to maintain the concentration gradient for glucose to passively enter cells.[13]
Knockout mice that are heterozygous for GLUT4 develop insulin resistance in their muscles as well as diabetes.[14]
Muscle contraction
Muscle contraction stimulates muscle cells to translocate GLUT4 receptors to their surfaces. This is especially true in cardiac muscle, where continuous contraction can be relied upon; but is observed to a lesser extent in skeletal muscle.[15] In skeletal muscle, muscle contraction increase GLUT4 translocation several fold [16] and this is likely regulated by RAC1 [17][18] and AMP-activated protein kinase.[19]
Muscle stretching
Muscle stretching also stimulate GLUT4 translocation and glucose uptake in rodent muscle via RAC1[20]
Interactions
GLUT4 has been shown to interact with death-associated protein 6.[21]
Interactive pathway map
Click on genes, proteins and metabolites below to link to respective articles. [§ 1]
Glycolysis and Gluconeogenesis edit
- ↑ The interactive pathway map can be edited at WikiPathways: "GlycolysisGluconeogenesis_WP534".
References
- ↑ James DE, Brown R, Navarro J, Pilch PF (May 1988). "Insulin-regulatable tissues express a unique insulin-sensitive glucose transport protein". Nature 333 (6169): 183–5. doi:10.1038/333183a0. PMID 3285221.
- ↑ James DE, Strube M, Mueckler M (Mar 1989). "Molecular cloning and characterization of an insulin-regulatable glucose transporter". Nature 338 (6210): 83–7. doi:10.1038/338083a0. PMID 2645527.
- ↑ Birnbaum MJ (Apr 1989). "Identification of a novel gene encoding an insulin-responsive glucose transporter protein". Cell 57 (2): 305–15. doi:10.1016/0092-8674(89)90968-9. PMID 2649253.
- ↑ Bell GI, Murray JC, Nakamura Y, Kayano T, Eddy RL, Fan YS, Byers MG, Shows TB (Aug 1989). "Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13". Diabetes 38 (8): 1072–5. doi:10.2337/diabetes.38.8.1072. PMID 2568955.
- ↑ Patel SS, Udayabanu M (Mar 2014). "Urtica dioica extract attenuates depressive like behavior and associative memory dysfunction in dexamethasone induced diabetic mice". Metabolic Brain Disease 29 (1): 121–30. doi:10.1007/s11011-014-9480-0. PMID 24435938.
- ↑ Piroli GG, Grillo CA, Reznikov LR, Adams S, McEwen BS, Charron MJ, Reagan LP (2007). "Corticosterone impairs insulin-stimulated translocation of GLUT4 in the rat hippocampus". Neuroendocrinology 85 (2): 71–80. doi:10.1159/000101694. PMID 17426391.
- ↑ Huang CC, Lee CC, Hsu KS (2010). "The role of insulin receptor signaling in synaptic plasticity and cognitive function". Chang Gung Medical Journal 33 (2): 115–25. PMID 20438663.
- ↑ Cushman SW, Wardzala LJ (May 1980). "Potential mechanism of insulin action on glucose transport in the isolated rat adipose cell. Apparent translocation of intracellular transport systems to the plasma membrane" (PDF). The Journal of Biological Chemistry 255 (10): 4758–62. PMID 6989818.
- ↑ Sonksen P, Sonksen J (Jul 2000). "Insulin: understanding its action in health and disease". British Journal of Anaesthesia 85 (1): 69–79. doi:10.1093/bja/85.1.69. PMID 10927996.
- ↑ JeBailey L, Wanono O, Niu W, Roessler J, Rudich A, Klip A (Feb 2007). "Ceramide- and oxidant-induced insulin resistance involve loss of insulin-dependent Rac-activation and actin remodeling in muscle cells". Diabetes 56 (2): 394–403. doi:10.2337/db06-0823. PMID 17259384.
- ↑ Sylow L, Kleinert M, Pehmøller C, Prats C, Chiu TT, Klip A, Richter EA, Jensen TE (Feb 2014). "Akt and Rac1 signaling are jointly required for insulin-stimulated glucose uptake in skeletal muscle and downregulated in insulin resistance". Cellular Signalling 26 (2): 323–31. doi:10.1016/j.cellsig.2013.11.007. PMID 24216610.
- 1 2 Sylow L, Jensen TE, Kleinert M, Højlund K, Kiens B, Wojtaszewski J, Prats C, Schjerling P, Richter EA (Jun 2013). "Rac1 signaling is required for insulin-stimulated glucose uptake and is dysregulated in insulin-resistant murine and human skeletal muscle". Diabetes 62 (6): 1865–75. doi:10.2337/db12-1148. PMC 3661612. PMID 23423567.
- ↑ Watson RT, Kanzaki M, Pessin JE (Apr 2004). "Regulated membrane trafficking of the insulin-responsive glucose transporter 4 in adipocytes". Endocrine Reviews 25 (2): 177–204. doi:10.1210/er.2003-0011. PMID 15082519.
- ↑ Stenbit AE, Tsao TS, Li J, Burcelin R, Geenen DL, Factor SM, Houseknecht K, Katz EB, Charron MJ (Oct 1997). "GLUT4 heterozygous knockout mice develop muscle insulin resistance and diabetes". Nature Medicine 3 (10): 1096–101. doi:10.1038/nm1097-1096. PMID 9334720.
- ↑ Lund S, Holman GD, Schmitz O, Pedersen O (Jun 1995). "Contraction stimulates translocation of glucose transporter GLUT4 in skeletal muscle through a mechanism distinct from that of insulin". Proceedings of the National Academy of Sciences of the United States of America 92 (13): 5817–21. doi:10.1073/pnas.92.13.5817. PMC 41592. PMID 7597034.
- ↑ Jensen TE, Sylow L, Rose AJ, Madsen AB, Angin Y, Maarbjerg SJ, Richter EA (Oct 2014). "Contraction-stimulated glucose transport in muscle is controlled by AMPK and mechanical stress but not sarcoplasmatic reticulum Ca(2+) release". Molecular Metabolism 3 (7): 742–53. doi:10.1016/j.molmet.2014.07.005. PMC 4209358. PMID 25353002.
- ↑ Sylow L, Møller LL, Kleinert M, Richter EA, Jensen TE (Dec 2014). "Rac1--a novel regulator of contraction-stimulated glucose uptake in skeletal muscle". Experimental Physiology 99 (12): 1574–80. doi:10.1113/expphysiol.2014.079194. PMID 25239922.
- ↑ Sylow L, Jensen TE, Kleinert M, Mouatt JR, Maarbjerg SJ, Jeppesen J, Prats C, Chiu TT, Boguslavsky S, Klip A, Schjerling P, Richter EA (Apr 2013). "Rac1 is a novel regulator of contraction-stimulated glucose uptake in skeletal muscle". Diabetes 62 (4): 1139–51. doi:10.2337/db12-0491. PMC 3609592. PMID 23274900.
- ↑ Mu J, Brozinick JT, Valladares O, Bucan M, Birnbaum MJ (May 2001). "A role for AMP-activated protein kinase in contraction- and hypoxia-regulated glucose transport in skeletal muscle". Molecular Cell 7 (5): 1085–94. PMID 11389854.
- ↑ Sylow L, Møller LL, Kleinert M, Richter EA, Jensen TE (Feb 2015). "Stretch-stimulated glucose transport in skeletal muscle is regulated by Rac1". The Journal of Physiology 593 (3): 645–56. doi:10.1113/jphysiol.2014.284281. PMC 4324711. PMID 25416624.
- ↑ Lalioti VS, Vergarajauregui S, Pulido D, Sandoval IV (May 2002). "The insulin-sensitive glucose transporter, GLUT4, interacts physically with Daxx. Two proteins with capacity to bind Ubc9 and conjugated to SUMO1". The Journal of Biological Chemistry 277 (22): 19783–91. doi:10.1074/jbc.M110294200. PMID 11842083.
Further reading
- Slot JW, Geuze HJ, Gigengack S, Lienhard GE, James DE (Apr 1991). "Immuno-localization of the insulin regulatable glucose transporter in brown adipose tissue of the rat". The Journal of Cell Biology 113 (1): 123–35. doi:10.1083/jcb.113.1.123. PMC 2288909. PMID 2007617.
- Govers R, Coster AC, James DE (Jul 2004). "Insulin increases cell surface GLUT4 levels by dose dependently discharging GLUT4 into a cell surface recycling pathway". Molecular and Cellular Biology 24 (14): 6456–66. doi:10.1128/MCB.24.14.6456-6466.2004. PMC 434240. PMID 15226445.
- Ng Y, Ramm G, Lopez JA, James DE (Apr 2008). "Rapid activation of Akt2 is sufficient to stimulate GLUT4 translocation in 3T3-L1 adipocytes". Cell Metabolism 7 (4): 348–56. doi:10.1016/j.cmet.2008.02.008. PMID 18396141.
- Foster LJ, Klip A (Oct 2000). "Mechanism and regulation of GLUT-4 vesicle fusion in muscle and fat cells". American Journal of Physiology. Cell Physiology 279 (4): C877–90. PMID 11003568.
- Bryant NJ, Govers R, James DE (Apr 2002). "Regulated transport of the glucose transporter GLUT4". Nature Reviews. Molecular Cell Biology 3 (4): 267–77. doi:10.1038/nrm782. PMID 11994746.
- Baumann MU, Deborde S, Illsley NP (Oct 2002). "Placental glucose transfer and fetal growth". Endocrine 19 (1): 13–22. doi:10.1385/ENDO:19:1:13. PMID 12583599.
- Olson AL, Knight JB (May 2003). "Regulation of GLUT4 expression in vivo and in vitro". Frontiers in Bioscience 8 (1-3): s401–9. doi:10.2741/1072. PMID 12700047.
- McCarthy AM, Elmendorf JS (Mar 2007). "GLUT4's itinerary in health & disease". The Indian Journal of Medical Research 125 (3): 373–88. PMID 17496362.
- Buse JB, Yasuda K, Lay TP, Seo TS, Olson AL, Pessin JE, Karam JH, Seino S, Bell GI (Nov 1992). "Human GLUT4/muscle-fat glucose-transporter gene. Characterization and genetic variation". Diabetes 41 (11): 1436–45. doi:10.2337/diabetes.41.11.1436. PMID 1397719.
- O'Rahilly S, Krook A, Morgan R, Rees A, Flier JS, Moller DE (May 1992). "Insulin receptor and insulin-responsive glucose transporter (GLUT 4) mutations and polymorphisms in a Welsh type 2 (non-insulin-dependent) diabetic population". Diabetologia 35 (5): 486–9. doi:10.1007/BF02342449. PMID 1521731.
- Liu ML, Olson AL, Moye-Rowley WS, Buse JB, Bell GI, Pessin JE (Jun 1992). "Expression and regulation of the human GLUT4/muscle-fat facilitative glucose transporter gene in transgenic mice". The Journal of Biological Chemistry 267 (17): 11673–6. PMID 1601840.
- Choi WH, O'Rahilly S, Buse JB, Rees A, Morgan R, Flier JS, Moller DE (Dec 1991). "Molecular scanning of insulin-responsive glucose transporter (GLUT4) gene in NIDDM subjects". Diabetes 40 (12): 1712–8. doi:10.2337/diabetes.40.12.1712. PMID 1756912.
- Kusari J, Verma US, Buse JB, Henry RR, Olefsky JM (Oct 1991). "Analysis of the gene sequences of the insulin receptor and the insulin-sensitive glucose transporter (GLUT-4) in patients with common-type non-insulin-dependent diabetes mellitus". The Journal of Clinical Investigation 88 (4): 1323–30. doi:10.1172/JCI115437. PMC 295602. PMID 1918382.
- Fukumoto H, Kayano T, Buse JB, Edwards Y, Pilch PF, Bell GI, Seino S (May 1989). "Cloning and characterization of the major insulin-responsive glucose transporter expressed in human skeletal muscle and other insulin-responsive tissues". The Journal of Biological Chemistry 264 (14): 7776–9. PMID 2656669.
- Chiaramonte R, Martini R, Taramelli R, Comi P (Aug 1993). "Identification of the 5' end of the gene encoding a human insulin-responsive glucose transporter". Gene 130 (2): 307–8. doi:10.1016/0378-1119(93)90438-9. PMID 7916714.
- Verhey KJ, Birnbaum MJ (Jan 1994). "A Leu-Leu sequence is essential for COOH-terminal targeting signal of GLUT4 glucose transporter in fibroblasts". The Journal of Biological Chemistry 269 (4): 2353–6. PMID 8300557.
- Lee W, Samuel J, Zhang W, Rampal AL, Lachaal M, Jung CY (Nov 1997). "A myosin-derived peptide C109 binds to GLUT4-vesicles and inhibits the insulin-induced glucose transport stimulation and GLUT4 recruitment in rat adipocytes". Biochemical and Biophysical Research Communications 240 (2): 409–14. doi:10.1006/bbrc.1997.7671. PMID 9388492.
- Shi Y, Samuel SJ, Lee W, Yu C, Zhang W, Lachaal M, Jung CY (Mar 1999). "Cloning of an L-3-hydroxyacyl-CoA dehydrogenase that interacts with the GLUT4 C-terminus". Archives of Biochemistry and Biophysics 363 (2): 323–32. doi:10.1006/abbi.1998.1088. PMID 10068455.
- Abel ED, Kaulbach HC, Tian R, Hopkins JC, Duffy J, Doetschman T, Minnemann T, Boers ME, Hadro E, Oberste-Berghaus C, Quist W, Lowell BB, Ingwall JS, Kahn BB (Dec 1999). "Cardiac hypertrophy with preserved contractile function after selective deletion of GLUT4 from the heart". The Journal of Clinical Investigation 104 (12): 1703–14. doi:10.1172/JCI7605. PMC 409881. PMID 10606624.
- Abel ED, Peroni O, Kim JK, Kim YB, Boss O, Hadro E, Minnemann T, Shulman GI, Kahn BB (Feb 2001). "Adipose-selective targeting of the GLUT4 gene impairs insulin action in muscle and liver". Nature 409 (6821): 729–33. doi:10.1038/35055575. PMID 11217863.
External links
- GLUT4 Protein at the US National Library of Medicine Medical Subject Headings (MeSH)
- USCD—Nature molecule pages: The signaling pathway", "GLUT4"; contains a high-resolution network map. Accessed 25 December 2009.
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||