EXPRESSION OF THE BRAIN-TYPE GLUCOSE TRANSPORTER IS RESTRICTED TO BRAIN AND NEURONAL CELLS IN MICE

被引:58
作者
GOULD, GW
BRANT, AM
KAHN, BB
SHEPHERD, PR
MCCOID, SC
GIBBS, EM
机构
[1] HARVARD UNIV,SCH MED,BOSTON,MA 02115
[2] BETH ISRAEL HOSP,BOSTON,MA 02215
[3] PFIZER INC,CENT RES,GROTON,CT 06340
基金
英国惠康基金;
关键词
GLUCOSE TRANSPORT; BRAIN-TYPE TRANSPORTER; DIABETES-MELLITUS;
D O I
10.1007/BF00401196
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Northern blot analysis of human tissues has demonstrated the expression of the brain-type glucose transporter isoform (GLUT 3) in liver, muscle and fat, raising the possibility that this transporter isoform may play a role in the regulation of glucose disposal in these tissues in response to insulin. We have raised an anti-peptide antibody against the C-terminal 13 amino acids of the murine homologue of this transporter isoform, and determined its tissue distribution in mouse tissues and murine-derived cell lines. The antibodies recognise a glycoprotein of about 50 kilodaltons, expressed at high levels in murine brain. In contrast to human tissues, the expression of GLUT 3 in mice is restricted to the brain, and no immunoreactivity was observed in either liver, fat or muscle membranes, or in murine 3T3-L1 fibroblasts or adipocytes. In contrast, high levels of expression of this isoform were observed in the NG 108 neuroblastoma x glioma cell line, a hybrid cell derived from rat glioma and mouse neuroblastoma cells. Taken together, these data suggest that the expression of GLUT 3 in rodents is restricted to non-insulin responsive neuronal cells and hence it is likely that the factors regulating the expression of this transporter in rodents differ to those in humans.
引用
收藏
页码:304 / 309
页数:6
相关论文
共 31 条
[1]   MOLECULAR-BIOLOGY OF MAMMALIAN GLUCOSE TRANSPORTERS [J].
BELL, GI ;
KAYANO, T ;
BUSE, JB ;
BURANT, CF ;
TAKEDA, J ;
LIN, D ;
FUKUMOTO, H ;
SEINO, S .
DIABETES CARE, 1990, 13 (03) :198-208
[2]   IDENTIFICATION OF A NOVEL GENE ENCODING AN INSULIN-RESPONSIVE GLUCOSE TRANSPORTER PROTEIN [J].
BIRNBAUM, MJ .
CELL, 1989, 57 (02) :305-315
[3]  
CALDERHEAD DM, 1990, J BIOL CHEM, V265, P13800
[4]   EXOFACIAL PHOTOLABELING OF THE HUMAN ERYTHROCYTE GLUCOSE TRANSPORTER WITH AN AZITRIFLUOROETHYLBENZOYL-SUBSTITUTED BISMANNOSE [J].
CLARK, AE ;
HOLMAN, GD .
BIOCHEMICAL JOURNAL, 1990, 269 (03) :615-622
[5]  
CLARKE DD, 1981, BASIC NEUROCHEMISTRY, P541
[6]   OBESE AND DIABETES - 2 MUTANT-GENES CAUSING DIABETES-OBESITY SYNDROMES IN MICE [J].
COLEMAN, DL .
DIABETOLOGIA, 1978, 14 (03) :141-148
[7]   THE BLOOD NERVE BARRIER IS RICH IN GLUCOSE TRANSPORTER [J].
FROEHNER, SC ;
DAVIES, A ;
BALDWIN, SA ;
LIENHARD, GE .
JOURNAL OF NEUROCYTOLOGY, 1988, 17 (02) :173-178
[8]  
FROST SC, 1985, J BIOL CHEM, V260, P2646
[9]   SEQUENCE, TISSUE DISTRIBUTION, AND CHROMOSOMAL LOCALIZATION OF MESSENGER-RNA ENCODING A HUMAN GLUCOSE TRANSPORTER-LIKE PROTEIN [J].
FUKUMOTO, H ;
SEINO, S ;
IMURA, H ;
SEINO, Y ;
EDDY, RL ;
FUKUSHIMA, Y ;
BYERS, MG ;
SHOWS, TB ;
BELL, GI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (15) :5434-5438
[10]   PRETRANSLATIONAL SUPPRESSION OF AN INSULIN-RESPONSIVE GLUCOSE TRANSPORTER IN RATS WITH DIABETES-MELLITUS [J].
GARVEY, WT ;
HUECKSTEADT, TP ;
BIRNBAUM, MJ .
SCIENCE, 1989, 245 (4913) :60-63