出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2013/11/12 11:40:44」(JST)
solute carrier family 2 (facilitated glucose transporter), member 2 | |
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Identifiers | |
Symbol | SLC2A2 |
Alt. symbols | GLUT2 |
Entrez | 6514 |
HUGO | 11006 |
OMIM | 138160 |
RefSeq | NM_000340 |
UniProt | P11168 |
Other data | |
Locus | Chr. 3 q26.2-q27 |
Glucose transporter 2 (GLUT2) also known as solute carrier family 2 (facilitated glucose transporter), member 2 (SLC2A2) is a transmembrane carrier protein that enables protein facilitated glucose movement across cell membranes. It is the principal transporter for transfer of glucose between liver and blood, and for renal glucose reabsorption. In humans, this protein is encoded by the SLC2A2 gene.[1][2] Unlike GLUT4, it does not rely on insulin for facilitated diffusion.
GLUT2 is found in cellular membranes of:
GLUT2 has high capacity for glucose but low affinity (high Km, ca. 15-20 mM) and thus functions as part of the "glucose sensor" in pancreatic β-cells. It is a very efficient carrier for glucose.[4][5]
GLUT2 also carries glucosamine.[6]
When the glucose concentration in the lumen of the small intestine goes above 30mM, such as occurs in the fed-state, GLUT2 is up-regulated at the brush border membrane, enhancing the capacity of glucose transport.
Defects in the SLC2A2 gene are associated with a particular type of glycogen storage disease called Fanconi-Bickel syndrome.[7]
In drug-treated diabetic pregnancies in which glucose levels in the woman are uncontrolled, neural tube and cardiac defects in the early-developing brain, spine, and heart depend upon functional GLUT2 carriers, and defects in the Glut2 gene have been shown to be protective against such defects in rats.[8] However, whilst a lack of GLUT2 adaptability[9] is negative, it is important to remember the fact that the main result of untreated gestational diabetes appears to cause babies to be of above-average size, which may well be an advantage that is managed very well with a healthy GLUT2 status.
Maintaining a regulated osmotic balance of sugar concentration between the blood circulation and the interstitial spaces is critical in some cases of edema including cerebral edema.
GLUT2 appears to be particularly important to osmoregulation, and preventing edema-induced stroke, transient ischemic attack or coma, especially when blood glucose concentration is above average.[10] GLUT2 could reasonably be referred to as the "diabetic glucose transporter" or a "stress hyperglycemia glucose transporter."
Click on genes, proteins and metabolites below to link to respective articles. [§ 1]
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リンク元 | 「グルコース」「グルコース輸送体」「ファンコニ・ビッケル症候群」「glucose transporter 2」「2型グルコース輸送体」 |
拡張検索 | 「VGLUT2」 |
関連記事 | 「GLUT」 |
SGLT1 | SGLT2 | |
局在 | 近位尿細管 | 近位尿細管 |
中間部(S2) | 起始部(S1) | |
終末部(S3) | ||
グルコースの親和性 | 高親和性 | 低親和性 |
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 | KM≒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→Vmax↑。KM=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
Fanconi-Bickel症候群 : 32 件 Fanconi-Bickle症候群 : ファンコニー・ビッケル症候群 : 5 件
2型グルコース輸送体、グルコース輸送体2、グルコーストランスポーター2
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