Literature DB >> 1704223

Tissue distribution and species difference of the brain type glucose transporter (GLUT3).

H Yano1, Y Seino, N Inagaki, Y Hinokio, T Yamamoto, K Yasuda, K Masuda, Y Someya, H Imura.   

Abstract

The complementary DNA for the human brain type glucose transporter (GLUT3) was used to determine its tissue specific expression in human, monkey, rabbit, rat, and mouse. Under high stringent conditions, 4.1 and 3.2 kilobase (kb) GLUT3 transcripts in monkey and a single 4.1 kb GLUT3 mRNA in rabbit, rat, and mouse were detected by RNA blot analysis. Although the GLUT3 transcripts were widely distributed, as are the erythrocyte type glucose transporter (GLUT1) transcripts, this mRNA is most abundant in the brain. However, the relative abundance of GLUT3 mRNA in the various regions of the monkey brain shows a different pattern from that of GLUT1 mRNA: GLUT3 is most highly expressed in the frontal lobe of the cerebrum, whereas GLUT1 is most abundant in the basal ganglia and the thalamus. Moderately higher GLUT3 mRNA levels were detected in the parietal lobe of the cerebrum, hippocampus, and cerebellum than the levels of GLUT1 transcripts. We also detected GLUT3 mRNA in adult human psoas major muscle, although it has been reported that the GLUT3 gene is scarcely expressed in adult human skeletal muscle of the thigh. In addition, in the rat and the mouse, no transcripts of the GLUT3 gene were detected in liver, kidney, small intestine, skeletal muscle, or fat besides in brain. Thus, the expression of the GLUT3 gene seems to be restricted to the brain in rodents. These results suggest that the expression of GLUT1 and GLUT3 genes might be regulated by different mechanisms.

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Year:  1991        PMID: 1704223     DOI: 10.1016/0006-291x(91)91440-n

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  22 in total

1.  Messenger RNA expression of transporter and ion channel genes in undifferentiated and differentiated Caco-2 cells compared to human intestines.

Authors:  Pascale Anderle; Vera Rakhmanova; Katie Woodford; Noa Zerangue; Wolfgang Sadée
Journal:  Pharm Res       Date:  2003-01       Impact factor: 4.200

2.  Neurons and microvessels express the brain glucose transporter protein GLUT3.

Authors:  D Z Gerhart; M A Broderius; N D Borson; L R Drewes
Journal:  Proc Natl Acad Sci U S A       Date:  1992-01-15       Impact factor: 11.205

3.  Regulation of glucose transporters (GLUT-1 and GLUT-3) in human retinal endothelial cells.

Authors:  R M Knott; M Robertson; E Muckersie; J V Forrester
Journal:  Biochem J       Date:  1996-08-15       Impact factor: 3.857

4.  The GLUT3 glucose transporter is the predominant isoform in primary cultured neurons: assessment by biosynthetic and photoaffinity labelling.

Authors:  F Maher; I A Simpson
Journal:  Biochem J       Date:  1994-07-15       Impact factor: 3.857

5.  Brain glucose transporter (Glut3) haploinsufficiency does not impair mouse brain glucose uptake.

Authors:  Charles A Stuart; Ian R Ross; Mary E A Howell; Melanie P McCurry; Thomas G Wood; Jeffrey D Ceci; Stephen J Kennel; Jonathan Wall
Journal:  Brain Res       Date:  2011-04-12       Impact factor: 3.252

6.  Functional properties and genomics of glucose transporters.

Authors:  Feng-Qi Zhao; Aileen F Keating
Journal:  Curr Genomics       Date:  2007-04       Impact factor: 2.236

7.  Attachment of PC12 cells to adhesion substratum induces the accumulation of glucose transporters (GLUTs) and stimulates glucose metabolism.

Authors:  D S Dwyer; H B Pinkofsky; Y Liu; R J Bradley
Journal:  Neurochem Res       Date:  1998-08       Impact factor: 3.996

8.  Glucose transporter gene expression in rat conceptus during high glucose culture.

Authors:  Y Takao; S Akazawa; K Matsumoto; H Takino; M Akazawa; R A Trocino; Y Maeda; S Okuno; E Kawasaki; S Uotani
Journal:  Diabetologia       Date:  1993-08       Impact factor: 10.122

9.  Regulation of glucose transporter (GLUT 3) and aldose reductase mRNA inbovine retinal endothelial cells and retinal pericytes in high glucose and high galactose culture.

Authors:  R M Knott; M Robertson; J V Forrester
Journal:  Diabetologia       Date:  1993-09       Impact factor: 10.122

10.  Implications of glucose transporter protein type 1 (GLUT1)-haplodeficiency in embryonic stem cells for their survival in response to hypoxic stress.

Authors:  Charles Heilig; Frank Brosius; Brian Siu; Luis Concepcion; Richard Mortensen; Kathleen Heilig; Min Zhu; Richard Weldon; Guimei Wu; David Conner
Journal:  Am J Pathol       Date:  2003-11       Impact factor: 4.307

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