RNA interface-mediated reduction in GLUT1 inhibits serum-induced glucose transport in primary human skeletal muscle cells

被引:25
作者
Al-Khalili, L
Cartee, GD
Krook, A [1 ]
机构
[1] Karolinska Inst, Dept Surg Sci, S-17177 Stockholm, Sweden
[2] Karolinska Inst, Dept Physiol & Pharmacol, S-17177 Stockholm, Sweden
[3] Univ Wisconsin, Dept Kinesiol, Madison, WI 53706 USA
关键词
RNA interference; human skeletal muscle; serum stimulation; glucose transport; GLUT1;
D O I
10.1016/S0006-291X(03)01124-0
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
Using RNA interference (RNAi), we specifically down-regulate protein expression in differentiated human skeletal myotube cultures. Serum stimulation of myotubes increases glucose uptake. Using a sensitive photolabeling technique, we demonstrate that this increase in glucose uptake is accompanied by increased cell-surface content of glucose transporter (GLUT) 1. Using RNAi, we specifically reduce GLUT1 mRNA and protein expression, leading to inhibition of serum-mediated increase in glucose transport. Thus, we demonstrate the utility of RNAi in a primary human differentiated cell system, and apply this methodology to demonstrate that serum-mediated increase in glucose transport in human skeletal muscle cells is dependent on GLUT1. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:127 / 132
页数:6
相关论文
共 39 条
[1]  
ALKHALILI L, 2003, IN PRESS CELL MOL LI
[2]  
ALKHALILI L, 2003, IN PRESS FEBS LETT
[3]   STIMULATION OF 2-DEOXYGLUCOSE UPTAKE IN GROWTH-INHIBITED BALB-C-3T3 AND REVERTANT SV40-TRANSFORMED 3T3-CELLS [J].
BRADLEY, WEC ;
CULP, LA .
EXPERIMENTAL CELL RESEARCH, 1974, 84 (1-2) :335-350
[4]   SERUM FACTOR INDUCES SELECTIVE INCREASE IN NA-CHANNEL EXPRESSION IN CULTURED SKELETAL-MUSCLE [J].
BRODIE, C ;
SAMPSON, SR .
JOURNAL OF CELLULAR PHYSIOLOGY, 1991, 148 (01) :48-53
[5]   A system for stable expression of short interfering RNAs in mammalian cells [J].
Brummelkamp, TR ;
Bernards, R ;
Agami, R .
SCIENCE, 2002, 296 (5567) :550-553
[6]   Inhibition of glycogen synthesis by fatty acid in C2C12 muscle cells is independent of PKC-α, -ε, and -θ [J].
Cazzolli, R ;
Craig, DL ;
Biden, TJ ;
Schmitz-Peiffer, C .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2002, 282 (06) :E1204-E1213
[7]   Gene silencing in Neurospora crassa requires a protein homologous to RNA-dependent RNA polymerase [J].
Cogoni, C ;
Macino, G .
NATURE, 1999, 399 (6732) :166-169
[8]  
DOUEN AG, 1990, J BIOL CHEM, V265, P13427
[9]   Duplexes of 21-nucleotide RNAs mediate RNA interference in cultured mammalian cells [J].
Elbashir, SM ;
Harborth, J ;
Lendeckel, W ;
Yalcin, A ;
Weber, K ;
Tuschl, T .
NATURE, 2001, 411 (6836) :494-498
[10]   Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans [J].
Fire, A ;
Xu, SQ ;
Montgomery, MK ;
Kostas, SA ;
Driver, SE ;
Mello, CC .
NATURE, 1998, 391 (6669) :806-811