Cellular stress causes accumulation of the glucose transporter at the surface of cells independently of their insulin sensitivity

被引:30
作者
Sviderskaya, EV
Jazrawi, E
Baldwin, SA
Widnell, CC
Pasternak, CA
机构
[1] UNIV LONDON ST GEORGES HOSP, SCH MED, DEPT CELLULAR & MOLEC SCI, LONDON SW17 0RE, ENGLAND
[2] UNIV LEEDS, DEPT BIOCHEM & MOLEC BIOL, LEEDS LS2 9JT, W YORKSHIRE, ENGLAND
[3] UNIV PITTSBURGH, SCH MED, DEPT CELL BIOL & PHYSIOL, PITTSBURGH, PA 15261 USA
基金
英国惠康基金;
关键词
cell surface; glucose transporter; GLUT1; GLUT4; insulin; stress;
D O I
10.1007/s002329900014
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
The stimulation of glucose transport in response to various types of stress has been studied. There is no relationship between effects of stress-inducing agents on glucose transport and their effects on cellular protein synthesis. Although the effect of stress on glucose transport appears analogous to its stimulation by insulin, cells that are slightly insulin-sensitive in terms of glucose transport (BHK cells) show a similar degree of stimulation as highly insulin-sensitive cells (differentiated 3T3-L1 cells). External labeling of the transporter protein with a photoactivatable derivative of mannose, 2-N-4-(1-azi-2,2,2-trifluoroethyl) benzoyl-1, 3-bis-(D-mannos-4-yloxy)-propylamine, shows that most of the increased glucose transport activity correlates with an increase in the amount of the transporter on the cell surface. Cells subjected to K+-depletion, which inhibits endocytosis and results in an accumulation of receptors at the cell surface, show the same increase in glucose transport as cells exposed to stress; stressed cells show no further increase in glucose transport when subjected to K+ depletion. These results support the view (Widnell, C.C., Baldwin, S.A., Davies, A., Martin, S., Pasternak, C.A. 1990. FASEB J 4:1634-1637) that cellular stress increases glucose transport by promoting the accumulation of glucose transporter molecules at the cell surface.
引用
收藏
页码:133 / 140
页数:8
相关论文
共 52 条
[1]   REGULATION OF GLUCOSE-TRANSPORT AND GLUT1 GLUCOSE TRANSPORTER EXPRESSION BY O2 IN MUSCLE-CELLS IN CULTURE [J].
BASHAN, N ;
BURDETT, E ;
HUNDAL, HS ;
KLIP, A .
AMERICAN JOURNAL OF PHYSIOLOGY, 1992, 262 (03) :C682-C690
[2]  
BELL GI, 1993, J BIOL CHEM, V268, P19161
[3]   HYPERTHERMIA, NA+K+ ATPASE AND LACTIC-ACID PRODUCTION IN SOME HUMAN-TUMOR CELLS [J].
BURDON, RH ;
KERR, SM ;
CUTMORE, CMM ;
MUNRO, J ;
GILL, V .
BRITISH JOURNAL OF CANCER, 1984, 49 (04) :437-445
[4]  
CAIN CC, 1992, J BIOL CHEM, V267, P11681
[5]  
CALDERHEAD DM, 1990, J BIOL CHEM, V265, P13800
[6]   DETERMINATION OF THE RATES OF APPEARANCE AND LOSS OF GLUCOSE TRANSPORTERS AT THE CELL-SURFACE OF RAT ADIPOSE-CELLS [J].
CLARK, AE ;
HOLMAN, GD ;
KOZKA, IJ .
BIOCHEMICAL JOURNAL, 1991, 278 :235-241
[7]  
CZECH MP, 1993, J BIOL CHEM, V268, P9187
[8]   2 THRESHOLD VALUS OF LOW PH BLOCK ENDOCYTOSIS AT DIFFERENT STAGES [J].
DAVOUST, J ;
GRUENBERG, J ;
HOWELL, KE .
EMBO JOURNAL, 1987, 6 (12) :3601-3609
[9]  
Diamond Deborah L., 1993, Glycobiology, V3, P542
[10]   MOLECULAR CHAPERONES [J].
ELLIS, RJ ;
VANDERVIES, SM .
ANNUAL REVIEW OF BIOCHEMISTRY, 1991, 60 :321-347