Peptide rescues GLUT4 recruitment, but not GLUT4 activation, in insulin resistance

被引:6
作者
Funaki, Makoto [1 ]
Benincasa, Kate [1 ]
Randhawa, Paramjeet K. [1 ]
机构
[1] Univ Penn, Vagelos Res Lab1142, Inst Med & Engn, Dept Physiol, Philadelphia, PA 19104 USA
关键词
GLUT4; GLUT1; recruitment to the plasma membrane; glucose uptake; insulin resistance; phosphoinositide-binding peptide;
D O I
10.1016/j.bbrc.2007.06.153
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
Insulin-stimulated GLUT4 recruitment to the plasma membrane is impaired in insulin resistance. We recently reported that a cell permeable phosphoinositide-binding peptide induces GLUT4 recruitment as potently as insulin, but does not activate GLUT4 to initiate glucose uptake. Here we investigated whether the peptide-induced GLUT4 recruitment is intact in insulin resistance. The expression levels of GLUT1 and GLUT4 were unaffected by chronically treating 3T3-L1 adipocytes with insulin. GLUT4 recruitment by acute insulin stimulation after chronic insulin treatment was significantly reduced, but was fully restored by the peptide treatment. However, subsequent acute insulin stimulation to activate GLUT4 failed to increase glucose uptake in peptide-pretreated cells. Insulin-stimulated GLUT1 recruitment was unaffected by the peptide pretreatment. These results suggest that the GLUT4 recruitment signal caused by the peptide is intact in insulin resistance, but GLUT4 activation that occurs subsequent to recruitment is not rescued by the peptide treatment. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:891 / 896
页数:6
相关论文
共 29 条
[21]   Indinavir uncovers different contributions of GLUT4 and GLUT1 towards glucose uptake in muscle and fat cells and tissues [J].
Rudich, A ;
Konrad, D ;
Török, D ;
Ben-Romano, R ;
Huang, C ;
Niu, W ;
Garg, RR ;
Wijesekara, N ;
Germinario, RJ ;
Bilan, PJ ;
Klip, A .
DIABETOLOGIA, 2003, 46 (05) :649-658
[22]   Intracellular mechanisms underlying increases in glucose uptake in response to insulin or exercise in skeletal muscle [J].
Ryder, JW ;
Chibalin, AV ;
Zierath, JR .
ACTA PHYSIOLOGICA SCANDINAVICA, 2001, 171 (03) :249-257
[23]   Mechanisms of disease - Glucose transporters and insulin action - Implications for insulin resistance and diabetes mellitus [J].
Shepherd, PR ;
Kahn, BB .
NEW ENGLAND JOURNAL OF MEDICINE, 1999, 341 (04) :248-257
[24]   ADIPOSE-TISSUE GLUCOSE TRANSPORTERS IN NIDDM - DECREASED LEVELS OF MUSCLE FAT ISOFORM [J].
SINHA, MK ;
RAINERIMALDONADO, C ;
BUCHANAN, C ;
PORIES, WJ ;
CARTERSU, C ;
PILCH, PF ;
CARO, JF .
DIABETES, 1991, 40 (04) :472-477
[25]   GENISTEIN INHIBITS INSULIN-STIMULATED GLUCOSE-TRANSPORT AND DECREASES IMMUNOCYTOCHEMICAL LABELING OF GLUT4 CARBOXYL-TERMINUS WITHOUT AFFECTING TRANSLOCATION OF GLUT4 IN ISOLATED RAT ADIPOCYTES - ADDITIONAL EVIDENCE OF GLUT4 ACTIVATION BY INSULIN [J].
SMITH, RM ;
TIESINGA, JJ ;
SHAH, N ;
SMITH, JA ;
JARETT, L .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1993, 300 (01) :238-246
[26]   IMMUNOELECTRON MICROSCOPIC DEMONSTRATION OF INSULIN-STIMULATED TRANSLOCATION OF GLUCOSE TRANSPORTERS TO THE PLASMA-MEMBRANE OF ISOLATED RAT ADIPOCYTES AND MASKING OF THE CARBOXYL-TERMINAL EPITOPE OF INTRACELLULAR GLUT4 [J].
SMITH, RM ;
CHARRON, MJ ;
SHAH, N ;
LODISH, HF ;
JARETT, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (15) :6893-6897
[27]   An inhibitor of p38 mitogen-activated protein kinase prevents insulin-stimulated glucose transport but not glucose transporter translocation in 3T3-L1 adipocytes and L6 myotubes [J].
Sweeney, G ;
Somwar, R ;
Ramlal, T ;
Volchuk, A ;
Ueyama, A ;
Klip, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (15) :10071-10078
[28]   Protein-protein interaction in insulin signaling and the molecular mechanisms of insulin resistance [J].
Virkamäki, A ;
Ueki, K ;
Kahn, CR .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (07) :931-943
[29]   Insulin action and insulin resistance in human skeletal muscle [J].
Zierath, JR ;
Krook, A ;
Wallberg-Henriksson, H .
DIABETOLOGIA, 2000, 43 (07) :821-835