Glucose transporter
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Glucose transporters (GLUT or SLC2A family) are a family of membrane proteins found in most mammalian cells.
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[edit] Function
Glucose is an essential substrate for the metabolism of most cells. Because glucose is a polar molecule, transport through biological membranes requires specific transport proteins. Transport of glucose through the apical membrane of intestinal and kidney epithelial cells depends on the presence of secondary active Na+/glucose symporters, SGLT-1 and SGLT-2, which concentrate glucose inside the cells, using the energy provided by cotransport of Na+ ions down their electrochemical gradient.[1] Facilitated diffusion of glucose through the cellular membrane is otherwise catalyzed by glucose carriers (protein symbol GLUT, gene symbol SLC2 for Solute Carrier Family 2) that belong to a superfamily of transport facilitators (major facilitator superfamily) including organic anion and cation transporters, yeast hexose transporter, plant hexose/proton symporters, and bacterial sugar/proton symporters.[2]
[edit] Structure
GLUTs are integral membrane proteins which contain 12 membrane-spanning helices with both the amino and carboxyl termini exposed on the cytoplasmic side of the plasma membrane. GLUT proteins transport glucose and related hexoses according to a model of alternate conformation,[3][4][5] which predicts that the transporter exposes a single substrate binding site toward either the outside or the inside of the cell. Binding of glucose to one site provokes a conformational change associated with transport, and releases glucose to the other side of the membrane. The inner and outer glucose-binding sites are probably located in transmembrane segments 9, 10, 11;[6] also, the QLS motif located in the seventh transmembrane segment could be involved in the selection and affinity of transported substrate.[7][8]
[edit] Types
Each glucose transporter isoform plays a specific role in glucose metabolism determined by its pattern of tissue expression, substrate specificity, transport kinetics, and regulated expression in different physiological conditions.[9] To date, 13 members of the GLUT/SLC2 have been identified.[10] On the basis of sequence similarities, the GLUT family has been divided into three subclasses.
[edit] Class I
Class I comprises the well-characterized glucose transporters GLUT1-GLUT4.[11]
- GLUT1 (SLC2A1) is widely distributed in fetal tissues. In the adult, it is expressed at highest levels in erythrocytes and also in the endothelial cells of barrier tissues such as the blood-brain barrier. However, it is responsible for the low-level of basal glucose uptake required to sustain respiration in all cells. Its levels in cell membranes are increased by reduced glucose levels and decreased by increased glucose levels.
- GLUT2 (SLC2A2) is expressed by renal tubular cells and small intestinal epithelial cells that transport glucose, liver cells and pancreatic β cells.
- GLUT3 (SLC2A3) is a high-affinity isoform expressed mostly in neurons where it is believed to be the main glucose transporter isoform, and in the placenta.
- GLUT4 (SLC2A4) is the insulin-regulated glucose transporter found in adipose tissues and striated muscle (skeletal and cardiac) that is responsible for insulin-regulated glucose disposal.
[edit] Classes II/III
Class II comprises the fructose transporter GLUT5 (SLC2A5) and GLUT7 (SLC2A7), 9 (SLC2A9), 11 (SLC2A11).
Class III comprises GLUT6 (SLC2A6), 8 (SLC2A8), 10 (SLC2A10), and 12 (SLC2A12) and the H+/myoinositol transporter HMIT (SLC2A13).[12]
Most members of classes II and III have been idenitified recently in homology searches of EST databases and the sequence information provided by the various genome projects.
[edit] Synthesis of free glucose
Most of cells are unable to produce free glucose because they lack expression of glucose-6-phosphatase and thus are only involved in glucose uptake and catabolism. Only hepatocytes and, in more severe fasting conditions, intestine and kidney, are able to produce glucose following activation of gluconeogenesis and glycogenolysis.
[edit] References
- ^ Hediger and Rhoads 1994
- ^ Henderson 1993
- ^ Oka et al. 1990
- ^ Hebert and Carruthers 1992
- ^ Cloherty et al. 1995
- ^ Hruz and Mueckler 2001
- ^ Seatter et al. 1998
- ^ Hruz and Mueckler 1999
- ^ Thorens 1996
- ^ Joost and Thorens 2001
- ^ Bell et al. 1990
- ^ Uldry et al. 2000
[edit] External links
ATP-binding cassette transporter - Amino acid (CD98) - Fatty acid (CD36) - Ion channels - Ion pumps - Mitochondrial membrane transport protein - Monosaccharide transport proteins (GLUT1, GLUT2, GLUT3, GLUT4) - Neurotransmitter transport proteins - Nuclear (Karyopherin)
