GLUT4
From Wikipedia, the free encyclopedia
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Solute carrier family 2 (facilitated glucose transporter), member 4
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| 'Effect of insulin on glucose uptake and metabolism.' Insulin binds to its receptor (1) which in turn starts many protein activation cascades (2). These include: translocation of Glut-4 transporter to the plasma membrane and influx of glucose (3), glycogen synthesis (4), glycolysis (5) and fatty acid synthesis (6). | ||||||||||||||
| Identifiers | ||||||||||||||
| Symbol(s) | SLC2A4; GLUT4 | |||||||||||||
| External IDs | OMIM: 138190 MGI: 95758 HomoloGene: 74381 | |||||||||||||
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| RNA expression pattern | ||||||||||||||
| Orthologs | ||||||||||||||
| Human | Mouse | |||||||||||||
| Entrez | 6517 | 20528 | ||||||||||||
| Ensembl | ENSG00000181856 | ENSMUSG00000018566 | ||||||||||||
| Uniprot | P14672 | Q5NCW7 | ||||||||||||
| Refseq | NM_001042 (mRNA) NP_001033 (protein) |
NM_009204 (mRNA) NP_033230 (protein) |
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| Location | Chr 17: 7.13 - 7.13 Mb | Chr 11: 69.76 - 69.76 Mb | ||||||||||||
| Pubmed search | [1] | [2] | ||||||||||||
GLUT4 is the insulin-regulated glucose transporter found in adipose tissues and striated muscle (skeletal and cardiac) that is responsible for insulin-regulated glucose disposal. It was discovered by Morris Birnbaum.[1]
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[edit] Reaction to insulin
In the absence of insulin, GLUT4 is sequestered in the interior of muscle and fat cells, within the lipid bilayer of vesicles.
Insulin induces the redistribution of GLUT4 from intracellular storage sites to the plasma membrane.
Once at the cell surface, GLUT4 facilitates the passive diffusion of circulating glucose down its concentration gradient into muscle and fat cells.
Once inside cells, glucose is rapidly phosphorylated by hexokinase to form glucose-6-phosphate, which then enters glycolysis.
Glucose-6-phosphate cannot diffuse back out of cells, which also serves to maintain the concentration gradient for glucose to passively enter cells.[2]
[edit] Pathway
The pathway in which GLUT4 is expressed on the plasma membrane begins with insulin binding to the receptor in its dimer form. The receptor phosphorylates and subsequently activates IRS-1, which converts PIP2 to PIP3. PIP3 is bound to PKB (protein kinase B), signaling for PDK1 to phosphorylate PKB. Once phosphorylated, PKB is in its active form and phosphorylates other targets that stimulate GLUT4 to be expressed on the plasma membrane.
[edit] Contraction
Contraction also stimulates the cell to translocate GLUT4 receptors to the surface. This is especially true in cardiac muscle, where continuous contraction can be relied upon; but is observed to a lesser extent in skeletal muscle. [3]
[edit] References
- ^ Birnbaum MJ (1989). "Identification of a novel gene encoding an insulin-responsive glucose transporter protein". Cell 57 (2): 305–15. PMID 2649253.
- ^ Watson RT, Kanzaki M, Pessin JE (2004). "Regulated membrane trafficking of the insulin-responsive glucose transporter 4 in adipocytes". Endocr. Rev. 25 (2): 177–204. PMID 15082519.
- ^ Lund S, Holman GD, Schmitz O, Pedersen O (1995). "Contraction stimulates translocation of glucose transporter GLUT4 in skeletal muscle through a mechanism distinct from that of insulin". Proc. Natl. Acad. Sci. U.S.A. 92 (13): 5817–21. PMID 7597034.
[edit] Further reading
- Foster LJ, Klip A (2000). "Mechanism and regulation of GLUT-4 vesicle fusion in muscle and fat cells.". Am. J. Physiol., Cell Physiol. 279 (4): C877–90. PMID 11003568.
- Bryant NJ, Govers R, James DE (2002). "Regulated transport of the glucose transporter GLUT4.". Nat. Rev. Mol. Cell Biol. 3 (4): 267–77. doi:. PMID 11994746.
- Baumann MU, Deborde S, Illsley NP (2003). "Placental glucose transfer and fetal growth.". Endocrine 19 (1): 13–22. PMID 12583599.
- Olson AL, Knight JB (2004). "Regulation of GLUT4 expression in vivo and in vitro.". Front. Biosci. 8: s401–9. PMID 12700047.
- McCarthy AM, Elmendorf JS (2007). "GLUT4's itinerary in health & disease.". Indian J. Med. Res. 125 (3): 373–88. PMID 17496362.
- Buse JB, Yasuda K, Lay TP, et al. (1992). "Human GLUT4/muscle-fat glucose-transporter gene. Characterization and genetic variation.". Diabetes 41 (11): 1436–45. PMID 1397719.
- O'Rahilly S, Krook A, Morgan R, et al. (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. PMID 1521731.
- Liu ML, Olson AL, Moye-Rowley WS, et al. (1992). "Expression and regulation of the human GLUT4/muscle-fat facilitative glucose transporter gene in transgenic mice.". J. Biol. Chem. 267 (17): 11673–6. PMID 1601840.
- Choi WH, O'Rahilly S, Buse JB, et al. (1992). "Molecular scanning of insulin-responsive glucose transporter (GLUT4) gene in NIDDM subjects.". Diabetes 40 (12): 1712–8. PMID 1756912.
- Kusari J, Verma US, Buse JB, et al. (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.". J. Clin. Invest. 88 (4): 1323–30. PMID 1918382.
- Bell GI, Murray JC, Nakamura Y, et al. (1989). "Polymorphic human insulin-responsive glucose-transporter gene on chromosome 17p13.". Diabetes 38 (8): 1072–5. PMID 2568955.
- Birnbaum MJ (1989). "Identification of a novel gene encoding an insulin-responsive glucose transporter protein.". Cell 57 (2): 305–15. PMID 2649253.
- Fukumoto H, Kayano T, Buse JB, et al. (1989). "Cloning and characterization of the major insulin-responsive glucose transporter expressed in human skeletal muscle and other insulin-responsive tissues.". J. Biol. Chem. 264 (14): 7776–9. PMID 2656669.
- Chiaramonte R, Martini R, Taramelli R, Comi P (1993). "Identification of the 5' end of the gene encoding a human insulin-responsive glucose transporter.". Gene 130 (2): 307–8. PMID 7916714.
- Verhey KJ, Birnbaum MJ (1994). "A Leu-Leu sequence is essential for COOH-terminal targeting signal of GLUT4 glucose transporter in fibroblasts.". J. Biol. Chem. 269 (4): 2353–6. PMID 8300557.
- Lee W, Samuel J, Zhang W, et al. (1997). "A myosin-derived peptide C109 binds to GLUT4-vesicles and inhibits the insulin-induced glucose transport stimulation and GLUT4 recruitment in rat adipocytes.". Biochem. Biophys. Res. Commun. 240 (2): 409–14. doi:. PMID 9388492.
- Shi Y, Samuel SJ, Lee W, et al. (1999). "Cloning of an L-3-hydroxyacyl-CoA dehydrogenase that interacts with the GLUT4 C-terminus.". Arch. Biochem. Biophys. 363 (2): 323–32. PMID 10068455.
- Abel ED, Kaulbach HC, Tian R, et al. (2000). "Cardiac hypertrophy with preserved contractile function after selective deletion of GLUT4 from the heart.". J. Clin. Invest. 104 (12): 1703–14. PMID 10606624.
- Abel ED, Peroni O, Kim JK, et al. (2001). "Adipose-selective targeting of the GLUT4 gene impairs insulin action in muscle and liver.". Nature 409 (6821): 729–33. doi:. PMID 11217863.

