Regulation of muscle GLUT-4 transcription by AMP-activated protein kinase

被引:214
作者
Zheng, DH
MacLean, PS
Pohnert, SC
Knight, JB
Olson, AL
Winder, WW
Dohm, GL [1 ]
机构
[1] E Carolina Univ, Brody Sch Med, Dept Biochem, Greenville, NC 27858 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Dept Biochem & Mol Biol, Oklahoma City, OK 73190 USA
[3] Brigham Young Univ, Dept Zool, Provo, UT 84602 USA
关键词
myocyte enhancer factor-2; GLUT-4; promoter; transgenic mice; muscle fiber type;
D O I
10.1152/jappl.2001.91.3.1073
中图分类号
Q4 [生理学];
学科分类号
071003 [生理学];
摘要
Skeletal muscle GLUT-4 transcription in response to treatment with 5-aminoimidazole-4-carboxamide-1-beta -D-ribofuranoside (AICAR), a known activator of AMP-activated protein kinase (AMPK), was studied in rats and mice. The increase in GLUT-4 mRNA levels in response to a single subcutaneous injection of AICAR, peaked at 13 h in white and red quadriceps muscles but not in the soleus muscle. The mRNA level of chloramphenicol acyltransferase reporter gene which is driven by 1,154 or 895 bp of the human GLUT-4 proximal promoter was increased in AICAR-treated transgenic mice, demonstrating the transcriptional upregulation of the GLUT-4 gene by AICAR. However, this induction of transcription was not apparent with 730 bp of the promoter. In addition, nuclear extracts from AICAR-treated mice bound to the consensus sequence of myocyte enhancer factor-2 (from -473 to -464) to a greater extent than from saline-injected mice. Thus AMP-activated protein kinase activation by AICAR increases GLUT-4 transcription by a mechanism that requires response elements within 895 bp of human GLUT-4 proximal promoter and that may be cooperatively mediated by myocyte enhancer factor-2.
引用
收藏
页码:1073 / 1083
页数:11
相关论文
共 52 条
[1]
Chronic treatment with 5-aminoimidazole-4-carboxamide-1-β-D-ribofuranoside increases insulin-stimulated glucose uptake and GLUT4 translocation in rat skeletal muscles in a fiber type-specific manner [J].
Buhl, ES ;
Jessen, N ;
Schmitz, O ;
Pedersen, SB ;
Pedersen, O ;
Holman, GD ;
Lund, S .
DIABETES, 2001, 50 (01) :12-17
[2]
CARLING D, 1994, J BIOL CHEM, V269, P11442
[3]
CARLSON M, 1981, GENETICS, V98, P25
[4]
Effect of aging on response to exercise training in humans: skeletal muscle GLUT-4 and insulin sensitivity [J].
Cox, JH ;
Cortright, RN ;
Dohm, GL ;
Houmard, JA .
JOURNAL OF APPLIED PHYSIOLOGY, 1999, 86 (06) :2019-2025
[6]
Regulated nuclear translocation of the Mig1 glucose repressor [J].
DeVit, MJ ;
Waddle, JA ;
Johnston, M .
MOLECULAR BIOLOGY OF THE CELL, 1997, 8 (08) :1603-1618
[7]
AMP-activated protein kinase inhibits the glucose-activated expression of fatty acid synthase gene in rat hepatocytes [J].
Foretz, M ;
Carling, D ;
Guichard, C ;
Ferré, P ;
Foufelle, F .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (24) :14767-14771
[8]
EXERCISE TRAINING INCREASES GLUCOSE TRANSPORTER PROTEIN GLUT-4 IN SKELETAL-MUSCLE OF OBESE ZUCKER (FA/FA) RATS [J].
FRIEDMAN, JE ;
SHERMAN, WM ;
REED, MJ ;
ELTON, CW ;
DOHM, GL .
FEBS LETTERS, 1990, 268 (01) :13-16
[9]
GLYCEMIC IMPROVEMENT IN DIABETIC DB/DB MICE BY OVEREXPRESSION OF THE HUMAN INSULIN-REGULATABLE GLUCOSE-TRANSPORTER (GLUT4) [J].
GIBBS, EM ;
STOCK, JL ;
MCCOID, SC ;
STUKENBROK, HA ;
PESSIN, JE ;
STEVENSON, RW ;
MILICI, AJ ;
MCNEISH, JD .
JOURNAL OF CLINICAL INVESTIGATION, 1995, 95 (04) :1512-1518
[10]
Exercise, glucose transport, and insulin sensitivity [J].
Goodyear, LJ ;
Kahn, BB .
ANNUAL REVIEW OF MEDICINE, 1998, 49 :235-261