GENE-EXPRESSION OF GLUT3 GLUCOSE-TRANSPORTER REGULATED BY GLUCOSE IN-VIVO IN MOUSE-BRAIN AND IN-VITRO IN NEURONAL CELL-CULTURES FROM RAT EMBRYOS

被引:61
作者
NAGAMATSU, S
SAWA, H
INOUE, N
NAKAMICHI, Y
TAKESHIMA, H
HOSHINO, T
机构
[1] KYORIN UNIV, SCH MED, DEPT NEUROSURG, MITAKA, TOKYO 181, JAPAN
[2] YOKOHAMA CITY UNIV, SCH MED, DEPT BIOCHEM, KANAZAWA KU, YOKOHAMA 236, JAPAN
关键词
D O I
10.1042/bj3000125
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study was designed to determine whether glucose regulates the gene expression of glucose transporter GLUT3 in neurons. We examined the regulation of GLUT3 mRNA by glucose in vivo in mouse brain and in vitro by using neuronal cultures from rat embryos. Hypoglycaemia (< 30 mg/dl), produced by 72 h of starvation, increased GLUT3 mRNA in mouse brain by 2-fold. Hybridization studies in situ demonstrated that hypoglycaemia-induced increases in GLUT3 mRNA expression were observed selectively in brain regions including the hippocampus, dentate gyrus, cerebral cortex and piriform cortex, but not the cerebellum. Primary neuronal cultures from rat embryos deprived of glucose for 48 h also showed an increase (4-fold over control) in GLUT3 mRNA, indicating that glucose can directly regulate expression of GLUT3 mRNA. In contrast with hypoglycaemia, hyperglycaemia produced by streptozotocin did not alter the expression of GLUT3 mRNA. We also confirmed previous findings that hypoglycaemia increases GLUT1 mRNA expression in brain. The increase in GLUT1 expression was probably limited to the blood-brain barrier in vivo, since GLUT1 mRNA could not be detected in neurons of the mouse cerebrum. Thus we conclude that up-regulation of neuronal GLUT3 in response to glucose starvation represents a protective mechanism against energy depletion in neurons.
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页码:125 / 131
页数:7
相关论文
共 46 条
[1]  
BODSCH W, 1984, CEREBRAL ISCHEMIA, P197
[2]  
BURANT CF, 1991, RECENT PROG HORM RES, V47, P349
[3]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[4]   BLOOD-BRAIN-BARRIER GLUCOSE TRANSPORTER MESSENGER-RNA IS INCREASED IN EXPERIMENTAL DIABETES-MELLITUS [J].
CHOI, TB ;
BOADO, RJ ;
PARDRIDGE, WM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1989, 164 (01) :375-380
[5]   STARVATION ACCELERATES BLOOD-BRAIN GLUCOSE TRANSFER [J].
CHRISTENSEN, TG ;
DIEMER, NH ;
LAURSEN, H ;
GJEDDE, A .
ACTA PHYSIOLOGICA SCANDINAVICA, 1981, 112 (02) :221-223
[6]   FACILITATED TRANSFER OF GLUCOSE FROM BLOOD INTO BRAIN TISSUE [J].
CRONE, C .
JOURNAL OF PHYSIOLOGY-LONDON, 1965, 181 (01) :103-&
[7]   DEFECTIVE GLUCOSE-TRANSPORT ACROSS THE BLOOD-BRAIN-BARRIER AS A CAUSE OF PERSISTENT HYPOGLYCORRHACHIA, SEIZURES, AND DEVELOPMENTAL DELAY [J].
DEVIVO, DC ;
TRIFILETTI, RR ;
JACOBSON, RI ;
RONEN, GM ;
BEHMAND, RA ;
HARIK, SI .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 325 (10) :703-709
[8]   BLOOD-BRAIN GLUCOSE TRANSFER - REPRESSION IN CHRONIC HYPERGLYCEMIA [J].
GJEDDE, A ;
CRONE, C .
SCIENCE, 1981, 214 (4519) :456-457
[9]   MODULATION OF SUBSTRATE TRANSPORT TO THE BRAIN [J].
GJEDDE, A .
ACTA NEUROLOGICA SCANDINAVICA, 1983, 67 (01) :3-25
[10]   DIRECT MEASUREMENT OF BRAIN GLUCOSE-CONCENTRATIONS IN HUMANS BY C-13 NMR-SPECTROSCOPY [J].
GRUETTER, R ;
NOVOTNY, EJ ;
BOULWARE, SD ;
ROTHMAN, DL ;
MASON, GF ;
SHULMAN, GI ;
SHULMAN, RG ;
TAMBORLANE, WV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (03) :1109-1112