Translocation of glucokinase in pancreatic beta-cells during acute and chronic hyperglycemia

被引:45
作者
Noma, Y
BonnerWeir, S
Latimer, JB
Davalli, AM
Weir, GC
机构
[1] DEACONESS HOSP, BOSTON, MA 02215 USA
[2] HARVARD UNIV, SCH MED, BOSTON, MA 02215 USA
[3] JOSLIN DIABET CTR, DIV RES, BOSTON, MA 02215 USA
[4] BRIGHAM & WOMENS HOSP, BOSTON, MA 02215 USA
关键词
D O I
10.1210/en.137.4.1485
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Glucokinase (GK) plays a key role in the regulation of glucose-induced insulin secretion, and questions have been raised about its relationship to the glucose transporter GLUT2 and its function in diabetes. This study examined the location of immunostained GK and GLUT2 in beta-cells using confocal microscopy. On double stained sections from pancreases of normal fed rats, GLUT2 Texas Red staining was restricted to the plasma membrane, and GK fluorescein isothiocyanate staining was found in a limited area of cytoplasm that was perinuclear with slight extension toward the apical pole. The GK staining occupied 8.6 +/- 1.7% of total cytoplasmic area and was almost never adjacent to the GLUT2 staining of the plasma membrane. To determine whether the GK staining pattern is altered by metabolic perturbation, normal rats were made acutely hyperglycemic with iv glucose injections; after 20 min the GK staining changed from being localized to become diffusely distributed throughout the cytoplasm. To examine the influence of chronic hyperglycemia, rats were subjected to 90% partial pancreatectomy (Px), which produced glucose levels of 10.9-20.8 mM. When studied 6 or 14 days after Px, those rats with glucose levels greater than 17.7 mM had an altered GK staining pattern that was variable; in some beta-cells GK staining was diffuse and in others the localized staining pattern was preserved. GLUT2 staining was reduced overall, but variability between cells was observed, unlike the more uniform reductions seen with hyperglycemia of longer duration. Other rats received islet transplants to prevent hyperglycemia after Px; their GK and GLUT2 staining patterns were normal. These findings indicate that GK is translocated in association with acute and chronic hyperglycemia. The translocation of this key enzyme for glucose recognition by beta-cells may lead to altered rates of insulin secretion during acute perturbations of fuel provision and in the diabetic state.
引用
收藏
页码:1485 / 1491
页数:7
相关论文
共 37 条
[1]   PORIN INTERACTION WITH HEXOKINASE AND GLYCEROL KINASE - METABOLIC MICROCOMPARTMENTATION AT THE OUTER MITOCHONDRIAL-MEMBRANE [J].
ADAMS, V ;
GRIFFIN, L ;
TOWBIN, J ;
GELB, B ;
WORLEY, K ;
MCCABE, ERB .
BIOCHEMICAL MEDICINE AND METABOLIC BIOLOGY, 1991, 45 (03) :271-291
[2]   INTRACELLULAR BINDING OF GLUCOKINASE IN HEPATOCYTES AND TRANSLOCATION BY GLUCOSE, FRUCTOSE AND INSULIN [J].
AGIUS, L ;
PEAK, M .
BIOCHEMICAL JOURNAL, 1993, 296 :785-796
[3]   CONTROL OF GLUCOKINASE TRANSLOCATION IN RAT HEPATOCYTES BY SORBITOL AND THE CYTOSOLIC REDOX STATE [J].
AGIUS, L .
BIOCHEMICAL JOURNAL, 1994, 298 :237-243
[4]   PARTIAL PANCREATECTOMY IN THE RAT AND SUBSEQUENT DEFECT IN GLUCOSE-INDUCED INSULIN RELEASE [J].
BONNERWEIR, S ;
TRENT, DF ;
WEIR, GC .
JOURNAL OF CLINICAL INVESTIGATION, 1983, 71 (06) :1544-1553
[5]   MORPHOLOGICAL EVIDENCE FOR PANCREATIC POLARITY OF BETA-CELL WITHIN ISLETS OF LANGERHANS [J].
BONNERWEIR, S .
DIABETES, 1988, 37 (05) :616-621
[6]  
BOSCO D, 1995, AM J PHYSIOL, V37, pC611
[7]   INTERACTION OF MUSCLE GLYCOLYTIC-ENZYMES WITH THIN FILAMENT PROTEINS [J].
BRONSTEIN, WW ;
KNULL, HR .
CANADIAN JOURNAL OF BIOCHEMISTRY, 1981, 59 (07) :494-499
[8]   REGULATORY EFFECTS OF GLUCOSE ON THE CATALYTIC ACTIVITY AND CELLULAR CONTENT OF GLUCOKINASE IN THE PANCREATIC BETA-CELL - STUDY USING CULTURED RAT ISLETS [J].
CHEN, C ;
HOSOKAWA, H ;
BUMBALO, LM ;
LEAHY, JL .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (04) :1616-1620
[9]   FUNCTION, MASS, AND REPLICATION OF PORCINE AND RAT ISLETS TRANSPLANTED INTO DIABETIC NUDE-MICE [J].
DAVALLI, AM ;
OGAWA, Y ;
SCAGLIA, L ;
WU, YJ ;
HOLLISTER, J ;
BONNERWEIR, S ;
WEIR, GC .
DIABETES, 1995, 44 (01) :104-111
[10]  
FERBER S, 1994, J BIOL CHEM, V269, P11523