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
[31]   SORTING OF MEMBRANE-COMPONENTS FROM ENDOSOMES AND SUBSEQUENT RECYCLING TO THE CELL-SURFACE OCCURS BY A BULK FLOW PROCESS [J].
MAYOR, S ;
PRESLEY, JF ;
MAXFIELD, FR .
JOURNAL OF CELL BIOLOGY, 1993, 121 (06) :1257-1269
[32]   FAMILY OF GLUCOSE-TRANSPORTER GENES - IMPLICATIONS FOR GLUCOSE-HOMEOSTASIS AND DIABETES [J].
MUECKLER, M .
DIABETES, 1990, 39 (01) :6-11
[33]  
OKADA T, 1994, J BIOL CHEM, V269, P3568
[34]   STRESS-INDUCED INCREASE OF HEXOSE-TRANSPORT AS A NOVEL INDEX OF CYTOPATHIC EFFECTS IN VIRUS-INFECTED CELLS - ROLE OF THE L-PROTEIN IN THE ACTION OF VESICULAR STOMATITIS-VIRUS [J].
PASTERNAK, CA ;
WHITAKERDOWLING, PA ;
WIDNELL, CC .
VIROLOGY, 1988, 166 (02) :379-386
[35]   REGULATION OF GLUCOSE-UPTAKE BY STRESSED CELLS [J].
PASTERNAK, CA ;
AIYATHURAI, JEJ ;
MAKINDE, V ;
DAVIES, A ;
BALDWIN, SA ;
KONIECZKO, EM ;
WIDNELL, CC .
JOURNAL OF CELLULAR PHYSIOLOGY, 1991, 149 (02) :324-331
[36]  
PASTERNAK CA, 1991, METH SURV I, V21, P391
[37]  
Pasternak Charles A., 1993, Glycobiology, V3, P542
[38]   THE EFFICIENT INTRACELLULAR SEQUESTRATION OF THE INSULIN-REGULATABLE GLUCOSE TRANSPORTER (GLUT-4) IS CONFERRED BY THE NH2 TERMINUS [J].
PIPER, RC ;
TAI, C ;
SLOT, JW ;
HAHN, CS ;
RICE, CM ;
HUANG, H ;
JAMES, DE .
JOURNAL OF CELL BIOLOGY, 1992, 117 (04) :729-743
[39]   HEAT-INDUCED STIMULATION OF 3-O-METHYLGLUCOSE TRANSPORT IN RAT THYMOCYTES [J].
REEVES, JP .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1977, 183 (01) :298-305
[40]   TRANSLOCATION OF THE GLUCOSE TRANSPORTER (GLUT4) TO THE CELL-SURFACE IN PERMEABILIZED 3T3-L1 ADIPOCYTES - EFFECTS OF ATP, INSULIN, AND GTP-GAMMA-S AND LOCALIZATION OF GLUT4 TO CLATHRIN LATTICES [J].
ROBINSON, LJ ;
PANG, SH ;
HARRIS, DS ;
HEUSER, J ;
JAMES, DE .
JOURNAL OF CELL BIOLOGY, 1992, 117 (06) :1181-1196