WordNet

a long truck for carrying motor vehicles (同)car transporter
a crane for moving material with dispatch as in loading and unloading ships
a monosaccharide sugar that has several forms; an important source of physiological energy

PrepTutorEJDIC

自動車運搬用大型トラック
ブドウ糖

Wikipedia preview

出典(authority):フリー百科事典『ウィキペディア（Wikipedia）』「2013/06/24 12:25:11」(JST)

wiki en

Glucose

Glucose transporters are a wide group of membrane proteins that facilitate the transport of glucose over a plasma membrane. Because glucose is a vital source of energy for all life these transporters are present in all phyla. The GLUT or SLC2A family are a protein family that is found in most mammalian cells.

Synthesis of free glucose [edit]

Most non-autotrophic cells are unable to produce free glucose because they lack expression of glucose-6-phosphatase and, thus, are involved only in glucose uptake and catabolism. Usually only produced in hepatocytes, in fasting conditions other tissues such as the intestines, muscles, brain and kidneys are able to produce glucose following activation of gluconeogenesis.

Glucose transport in yeast [edit]

In Saccharomyces cerevisiae glucose transport takes place through facilitated diffusion.^[1] The transport proteins are mainly from the Hxt family, but many other transporters have been identified.^[2]

Name	Properties	Notes
Snf3		low-glucose sensor; repressed by glucose; low expression level; repressor of Hxt6
Rgt2		high-glucose sensor; low expression level
Hxt1	Km: 100 mM,^[3] 129 - 107 mM^[1]	low-affinity glucose transporter; induced by high glucose level
Hxt2	Km = 1.5^[1] - 10 mM^[3]	high/intermediate-affinityglucose transporter; induced by low glucose level^[3]
Hxt3	Vm = 18.5, Kd = 0.078, Km = 28.6/34.2^[1] - 60 mM^[3]	low-affinity glucose transporter^[3]
Hxt4	Vm = 12.0, Kd = 0.049, Km = 6.2^[1]	intermediate-affinity glucose transporter^[3]
Hxt5	Km = 10 mM^[4]	Moderate glucose affinity. Abundant during stationary phase, sporulation and low glucose conditions. Transcription repressed by glucose.^[4]
Hxt6	Vm = 11.4, Kd = 0.029, Km = 0.9/14,^[1] 1.5 mM^[3]	high glucose affinity^[3]
Hxt7	Vm = 11.7, Kd = 0.039, Km = 1.3, 1.9,^[1] 1.5 mM^[3]	high glucose affinity^[3]
Hxt8		low expression level^[3]
Hxt9		involved in pleiotropic drug resistance^[3]
Hxt11		involved in pleiotropic drug resistance^[3]
Gal2	Vm = 17.5, Kd = 0.043, Km = 1.5, 1.6^[1]	high galactose affinity^[3]

Glucose transport in Mammals [edit]

GLUTs are integral membrane proteins that 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,^[5]^[6]^[7] 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, it seems, located in transmembrane segments 9, 10, 11;^[8] also, the QLS motif located in the seventh transmembrane segment could be involved in the selection and affinity of transported substrate.^[9]^[10]

Types [edit]

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.^[11] To date, 13 members of the GLUT/SLC2 have been identified.^[12] On the basis of sequence similarities, the GLUT family has been divided into three subclasses.

Class I [edit]

Class I comprises the well-characterized glucose transporters GLUT1-GLUT4.^[13]

Name	Distribution	Notes
GLUT1	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.	Levels in cell membranes are increased by reduced glucose levels and decreased by increased glucose levels.
GLUT2	Is a bidirectional transporter, allowing glucose to flow in 2 directions. Is expressed by renal tubular cells, small intestinal epithelial cells, liver cells and pancreatic beta cells. It is also present in the basolateral membrane of the small intestine epithelium. Bidirectionality is required in liver cells to uptake glucose for glycolysis, and release of glucose during gluconeogenesis. In pancreatic beta cells, free flowing glucose is required so that the intracellular environment of these cells can accurately gauge the serum glucose levels. All three monosaccharides (glucose, galactose and fructose) are transported from the intestinal mucosal cell into the portal circulation by GLUT2	Is a high-capacity and low-affinity isoform. There is some evidence^{[citation needed]} that GLUT 1 and 3 are actually the functional transporters in beta cells.
GLUT3	Expressed mostly in neurons (where it is believed to be the main glucose transporter isoform), and in the placenta.	Is a high-affinity isoform, allowing it to transport even in times of low glucose concentrations.
GLUT4	Found in adipose tissues and striated muscle (skeletal muscle and cardiac muscle).	Is the insulin-regulated glucose transporter. Responsible for insulin-regulated glucose storage.

Classes II/III [edit]

Class II comprises:

GLUT5 (SLC2A5), a fructose transporter
GLUT7 - SLC2A7 - (SLC2A7), transporting glucose out of the endoplasmic reticulum ^[14]
GLUT9 - SLC2A9 - (SLC2A9)
GLUT11 (SLC2A11)

Class III comprises:

GLUT6 (SLC2A6),
GLUT8 (SLC2A8),
GLUT10 (SLC2A10),
GLUT12 (SLC2A12), and
the H+/myoinositol transporter HMIT (SLC2A13).^[15]

Most members of classes II and III have been identified recently in homology searches of EST databases and the sequence information provided by the various genome projects.

The function of these new glucose transporter isoforms is still not clearly defined at present. Several of them (GLUT6, GLUT8) are made of motifs that help retain them intracellularly and therefore prevent glucose transport. Whether mechanisms exist to promote cell-surface translocation of these transporters is not yet known, but it has clearly been established that insulin does not promote GLUT6 and GLUT8 cell-surface translocation.

Discovery of sodium-glucose cotransport [edit]

In August 1960, in Prague, Robert K. Crane presented for the first time his discovery of the sodium-glucose cotransport as the mechanism for intestinal glucose absorption.^[16] Crane's discovery of cotransport was the first ever proposal of flux coupling in biology.^[17]^[18]

References [edit]

^ ^a ^b ^c ^d ^e ^f ^g ^h Maier A, Asano T, Volker A, Boles E, Fuhrmann G F (2002). "Characterisation of glucose transport in Saccharomyces cerevisiae with plasma membrane vesicles (countertransport) and intact cells (initial uptake) with single Hxt1, Hxt2, Hxt3, Hxt4, Hxt6, Hxt7 or Gal2 transporters". FEMS Yeast Research 2 (4): 539–550. doi:10.1111/j.1567-1364.2002.tb00121.x. PMID 12702270.
^ uniprot list of possible glucose transporters in S. cerevisiae
^ ^a ^b ^c ^d ^e ^f ^g ^h ⁱ ^j ^k ^l ^m ⁿ Boles E, Hollenberg C P (1997). "The molecular genetics of hexose transport in yeasts". FEMS Microbiology Reviews 21 (1): 85–111. doi:10.1111/j.1574-6976.1997.tb00346.x. PMID 9299703.
^ ^a ^b Diderich J A, Schuurmans J M, Gaalen M C, Kruckeberg A L, Van Dam K (2001). "Functional analysis of the hexose transporter homologue HXT5 in Saccharomyces cerevisiae". Yeast 18 (16): 1515–1524. doi:10.1002/yea.779. PMID 11748728.
^ Oka Y, Asano T, Shibasaki Y, Lin J, Tsukuda K, Katagiri H, Akanuma Y, Takaku F (1990). "C-terminal truncated glucose transporter is locked into an inward-facing form without transport activity". Nature 345 (6275): 550–3. doi:10.1038/345550a0. PMID 2348864.
^ Hebert D, Carruthers A (1992). "Glucose transporter oligomeric structure determines transporter function. Reversible redox-dependent interconversions of tetrameric and dimeric GLUT1". J. Biol. Chem. 267 (33): 23829–38. PMID 1429721.
^ Cloherty E, Sultzman L, Zottola R, Carruthers A (1995). "Net sugar transport is a multistep process. Evidence for cytosolic sugar binding sites in erythrocytes". Biochemistry 34 (47): 15395–406. doi:10.1021/bi00047a002. PMID 7492539.
^ Hruz P, Mueckler M (2001). "Structural analysis of the GLUT1 facilitative glucose transporter (review)". Mol. Membr. Biol. 18 (3): 183–93. doi:10.1080/09687680110072140. PMID 11681785.
^ Seatter M, De la Rue S, Porter L, Gould G (1998). "QLS motif in transmembrane helix VII of the glucose transporter family interacts with the C-1 position of D-glucose and is involved in substrate selection at the exofacial binding site". Biochemistry 37 (5): 1322–6. doi:10.1021/bi972322u. PMID 9477959.
^ Hruz P, Mueckler M (1999). "Cysteine-scanning mutagenesis of transmembrane segment 7 of the GLUT1 glucose transporter". J. Biol. Chem. 274 (51): 36176–80. doi:10.1074/jbc.274.51.36176. PMID 10593902.
^ Thorens B (1996). "Glucose transporters in the regulation of intestinal, renal, and liver glucose fluxes". Am. J. Physiol. 270 (4 Pt 1): G541–53. PMID 8928783.
^ Joost H, Thorens B (2001). "The extended GLUT-family of sugar/polyol transport facilitators: nomenclature, sequence characteristics, and potential function of its novel members (review)". Mol. Membr. Biol. 18 (4): 247–56. doi:10.1080/09687680110090456. PMID 11780753.
^ Bell G, Kayano T, Buse J, Burant C, Takeda J, Lin D, Fukumoto H, Seino S (1990). "Molecular biology of mammalian glucose transporters". Diabetes Care 13 (3): 198–208. doi:10.2337/diacare.13.3.198. PMID 2407475.
^ Page 995 in: Walter F., PhD. Boron (2003). Medical Physiology: A Cellular And Molecular Approaoch. Elsevier/Saunders. p. 1300. ISBN 1-4160-2328-3.
^ Uldry M, Thorens B (2004). "The SLC2 family of facilitated hexose and polyol transporters". Pflugers Arch. 447 (5): 480–9. doi:10.1007/s00424-003-1085-0. PMID 12750891.
^ Robert K. Crane, D. Miller and I. Bihler. “The restrictions on possible mechanisms of intestinal transport of sugars”. In: Membrane Transport and Metabolism. Proceedings of a Symposium held in Prague, August 22–27, 1960. Edited by A. Kleinzeller and A. Kotyk. Czech Academy of Sciences, Prague, 1961, pp. 439-449.
^ Ernest M. Wright and Eric Turk. “The sodium glucose cotransport family SLC5”. Pflügers Arch 447, 2004, p. 510. “Crane in 1961 was the first to formulate the cotransport concept to explain active transport [7]. Specifically, he proposed that the accumulation of glucose in the intestinal epithelium across the brush border membrane was [is] coupled to downhill Na+ transport cross the brush border. This hypothesis was rapidly tested, refined, and extended [to] encompass the active transport of a diverse range of molecules and ions into virtually every cell type.”
^ Boyd, C A R. “Facts, fantasies and fun in epithelial physiology”. Experimental Physiology, Vol. 93, Issue 3, 2008, p. 304. “the insight from this time that remains in all current text books is the notion of Robert Crane published originally as an appendix to a symposium paper published in 1960 (Crane et al. 1960). The key point here was 'flux coupling', the cotransport of sodium and glucose in the apical membrane of the small intestinal epithelial cell. Half a century later this idea has turned into one of the most studied of all transporter proteins (SGLT1), the sodium–glucose cotransporter.”

External links [edit]

Glucose Transport Proteins, Facilitative at the US National Library of Medicine Medical Subject Headings (MeSH)

UpToDate Contents

全文を閲覧するには購読必要です。 To read the full text you will need to subscribe.

1. グルコースおよびグリコーゲン代謝の遺伝性疾患の概要 overview of inherited disorders of glucose and glycogen metabolism
2. グリコーゲン代謝のその他の障害：GLUT2欠損症およびアルドラーゼA欠損症 other disorders of glycogen metabolism glut2 deficiency and aldolase a deficiency
3. 成人糖尿病患者のマネージメントにおける血糖の自己モニタリング（SMBG） blood glucose self monitoring in management of adults with diabetes mellitus
4. グルコース-6-ホスファターゼ欠損症（糖原病I型、フォンギールケ病） glucose 6 phosphatase deficiency glycogen storage disease i von gierke disease
5. 健常被験者および糖尿病患者における低血糖に対する生理的応答 physiologic response to hypoglycemia in normal subjects and patients with diabetes mellitus

English Journal

Ca2+ regulation of mitochondrial function in neurons.

Rueda CB1, Llorente-Folch I1, Amigo I1, Contreras L1, González-Sánchez P1, Martínez-Valero P1, Juaristi I1, Pardo B1, Del Arco A2, Satrústegui J3.
Biochimica et biophysica acta.Biochim Biophys Acta.2014 Oct;1837(10):1617-1624. doi: 10.1016/j.bbabio.2014.04.010. Epub 2014 May 10.
Calcium is thought to regulate respiration but it is unclear whether this is dependent on the increase in ATP demand caused by any Ca2+ signal or to Ca2+ itself. [Na+]i, [Ca2+]i and [ATP]i dynamics in intact neurons exposed to different workloads in the absence and presence of Ca2+ clearly showed th
PMID 24820519

Extra-nuclear telomerase reverse transcriptase (TERT) regulates glucose transport in skeletal muscle cells.

Shaheen F1, Grammatopoulos DK2, Müller J3, Zammit VA4, Lehnert H5.
Biochimica et biophysica acta.Biochim Biophys Acta.2014 Sep;1842(9):1762-9. doi: 10.1016/j.bbadis.2014.06.018. Epub 2014 Jun 23.
Telomerase reverse transcriptase (TERT) is a key component of the telomerase complex. By lengthening telomeres in DNA strands, TERT increases senescent cell lifespan. Mice that lack TERT age much faster and exhibit age-related conditions such as osteoporosis, diabetes and neurodegeneration. Accelera
PMID 24970747

Japanese Journal

Sugar consumption and ethanol fermentation by transporter-overexpressed xylose-metabolizing Saccharomyces cerevisiae harboring a xyloseisomerase pathway(BIOCHEMICAL ENGINEERING)

Tanino Takanori,Ito Tomonori,Ogino Chiaki,Ohmura Naoto,Ohshima Takayuki,Kondo Akihiko
Journal of bioscience and bioengineering 114(2), 209-211, 2012-08
… Four kinds of transporters, HXT1 and HXY7 from Saccharomyces cerevisiae, and GXFI and GXSI from Candida inter- media, were overexpressed in xylose-metabolizing S. … Over- expression of transporter enhanced sugar consumption and ethanol production, and GXF1 was efficient for ethanol fermentation from both glucose and xylose. …
NAID 110009495431

Select Nutrients in the Uterine Lumen of Sheep and Pigs Affect Conceptus Development

BAZER Fuller W.,KIM Jinyoung,KA Hakhyun,JOHNSON Gregory A.,WU Guoyao,SONG Gwonhwa
The Journal of reproduction and development 58(2), 180-188, 2012-04-01
… IFNT also acts with P4 to induce expression of genes for transport of nutrients, such as glucose (Gluc) and arginine (Arg) into the uterine lumen to activate mechanistic mammalian target of rapamycin (MTOR) cell signaling that stimulates proliferation, migration, gene transcription and mRNA translation by conceptus trophectoderm (Tr). …
NAID 10030753562

Related Pictures

Biology of Human Sodium Glucose Transporters | Physiological Reviews Glucose Transporter 3 Potentiates Degranulation and Is Required for Platelet 063-Glucose Transporter & Co-transporters - YouTube glucose transporters | The cell, Biology, Glucose Glucose is absorbed in the small intestine by a secondary active transport mechanism Glut 2 y glut 4 GLUCOSE TRANSPORTERS - www.medicoapps.org PPT - Metabolism of cardiac muscle PowerPoint Presentation, free

★リンクテーブル★

リンク元	「グルコース輸送体」「GLUT」
関連記事	「transporter」

「グルコース輸送体」

Available protein structures:
Pfam	structures
PDB	RCSB PDB; PDBe
PDBsum	structure summary

Sugar_tr
Identifiers
Symbol	Sugar_tr
Pfam	PF00083
Pfam clan	CL0015
InterPro	IPR005828
PROSITE	PDOC00190
TCDB	2.A.1.1
OPM superfamily	15
OPM protein	4gc0
Available protein structures:
Pfam	structures
PDB	RCSB PDB; PDBe
PDBsum	structure summary

　　[★]

英: glucose transporter, GLUT, glucose transporters
同: ブドウ糖輸送担体、糖輸送体糖輸送担体 sugar transporter

グルコースの促通拡散を担う

GLUTの種類

GLUT	発現部位	機能
GLUT1	赤血球、脳、筋肉、脂肪、その他。×肝臓
GLUT2	肝臓、脾臓β細胞	K_M≒60mM、hexokinase IV(glucokinase)(50kDa)
GLUT3	脳、神経	グルコース需要が多い場所で発現
GLUT4	筋と脂肪組織のみ	インスリン→V_max↑。K_M=2-5mM、hexokinase II(100kDa)
GLUT5	小腸上皮管腔側	フルクトースの受動輸送
GLUT7	肝臓小胞体	G6Pの脱リン酸化に関与(FB. 453)

-GLUT

-GLUT

「GLUT」

　　[★] グルコース輸送体 glucose transporter glucose transporters

「transporter」

　　[★] トランスポーター

関: translocator、transport protein、transporter protein

[Maier-1] ^ ^a ^b ^c ^d ^e ^f ^g ^h Maier A, Asano T, Volker A, Boles E, Fuhrmann G F (2002). "Characterisation of glucose transport in Saccharomyces cerevisiae with plasma membrane vesicles (countertransport) and intact cells (initial uptake) with single Hxt1, Hxt2, Hxt3, Hxt4, Hxt6, Hxt7 or Gal2 transporters". FEMS Yeast Research 2 (4): 539–550. doi:10.1111/j.1567-1364.2002.tb00121.x. PMID 12702270.

[2] uniprot list of possible glucose transporters in S. cerevisiae

[molgen-3] ^ ^a ^b ^c ^d ^e ^f ^g ^h ⁱ ^j ^k ^l ^m ⁿ Boles E, Hollenberg C P (1997). "The molecular genetics of hexose transport in yeasts". FEMS Microbiology Reviews 21 (1): 85–111. doi:10.1111/j.1574-6976.1997.tb00346.x. PMID 9299703.

[SILS-4] Diderich J A, Schuurmans J M, Gaalen M C, Kruckeberg A L, Van Dam K (2001). "Functional analysis of the hexose transporter homologue HXT5 in Saccharomyces cerevisiae". Yeast 18 (16): 1515–1524. doi:10.1002/yea.779. PMID 11748728.

[5] Oka Y, Asano T, Shibasaki Y, Lin J, Tsukuda K, Katagiri H, Akanuma Y, Takaku F (1990). "C-terminal truncated glucose transporter is locked into an inward-facing form without transport activity". Nature 345 (6275): 550–3. doi:10.1038/345550a0. PMID 2348864.

[6] Hebert D, Carruthers A (1992). "Glucose transporter oligomeric structure determines transporter function. Reversible redox-dependent interconversions of tetrameric and dimeric GLUT1". J. Biol. Chem. 267 (33): 23829–38. PMID 1429721.

[7] Cloherty E, Sultzman L, Zottola R, Carruthers A (1995). "Net sugar transport is a multistep process. Evidence for cytosolic sugar binding sites in erythrocytes". Biochemistry 34 (47): 15395–406. doi:10.1021/bi00047a002. PMID 7492539.

[8] Hruz P, Mueckler M (2001). "Structural analysis of the GLUT1 facilitative glucose transporter (review)". Mol. Membr. Biol. 18 (3): 183–93. doi:10.1080/09687680110072140. PMID 11681785.

[9] Seatter M, De la Rue S, Porter L, Gould G (1998). "QLS motif in transmembrane helix VII of the glucose transporter family interacts with the C-1 position of D-glucose and is involved in substrate selection at the exofacial binding site". Biochemistry 37 (5): 1322–6. doi:10.1021/bi972322u. PMID 9477959.

[10] Hruz P, Mueckler M (1999). "Cysteine-scanning mutagenesis of transmembrane segment 7 of the GLUT1 glucose transporter". J. Biol. Chem. 274 (51): 36176–80. doi:10.1074/jbc.274.51.36176. PMID 10593902.

[11] Thorens B (1996). "Glucose transporters in the regulation of intestinal, renal, and liver glucose fluxes". Am. J. Physiol. 270 (4 Pt 1): G541–53. PMID 8928783.

[12] Joost H, Thorens B (2001). "The extended GLUT-family of sugar/polyol transport facilitators: nomenclature, sequence characteristics, and potential function of its novel members (review)". Mol. Membr. Biol. 18 (4): 247–56. doi:10.1080/09687680110090456. PMID 11780753.

[13] Bell G, Kayano T, Buse J, Burant C, Takeda J, Lin D, Fukumoto H, Seino S (1990). "Molecular biology of mammalian glucose transporters". Diabetes Care 13 (3): 198–208. doi:10.2337/diacare.13.3.198. PMID 2407475.

[boron995-14] Page 995 in: Walter F., PhD. Boron (2003). Medical Physiology: A Cellular And Molecular Approaoch. Elsevier/Saunders. p. 1300. ISBN 1-4160-2328-3.

[15] Uldry M, Thorens B (2004). "The SLC2 family of facilitated hexose and polyol transporters". Pflugers Arch. 447 (5): 480–9. doi:10.1007/s00424-003-1085-0. PMID 12750891.

[16] Robert K. Crane, D. Miller and I. Bihler. “The restrictions on possible mechanisms of intestinal transport of sugars”. In: Membrane Transport and Metabolism. Proceedings of a Symposium held in Prague, August 22–27, 1960. Edited by A. Kleinzeller and A. Kotyk. Czech Academy of Sciences, Prague, 1961, pp. 439-449.

[17] Ernest M. Wright and Eric Turk. “The sodium glucose cotransport family SLC5”. Pflügers Arch 447, 2004, p. 510. “Crane in 1961 was the first to formulate the cotransport concept to explain active transport [7]. Specifically, he proposed that the accumulation of glucose in the intestinal epithelium across the brush border membrane was [is] coupled to downhill Na+ transport cross the brush border. This hypothesis was rapidly tested, refined, and extended [to] encompass the active transport of a diverse range of molecules and ions into virtually every cell type.”

[18] Boyd, C A R. “Facts, fantasies and fun in epithelial physiology”. Experimental Physiology, Vol. 93, Issue 3, 2008, p. 304. “the insight from this time that remains in all current text books is the notion of Robert Crane published originally as an appendix to a symposium paper published in 1960 (Crane et al. 1960). The key point here was 'flux coupling', the cotransport of sodium and glucose in the apical membrane of the small intestinal epithelial cell. Half a century later this idea has turned into one of the most studied of all transporter proteins (SGLT1), the sodium–glucose cotransporter.”

匿名

検索

案内

案内

glucose transporters