Molecular Mechanisms for the Regulation of Insulin-Stimulated Glucose Uptake by Small Guanosine Triphosphatases in Skeletal Muscle and Adipocytes

被引:88
作者
Satoh, Takaya [1 ]
机构
[1] Osaka Prefecture Univ, Grad Sch Sci, Dept Biol Sci, Lab Cell Biol,Naka Ku, Sakai, Osaka 5998531, Japan
来源
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | 2014年 / 15卷 / 10期
关键词
adipocyte; glucose uptake; GLUT4; insulin; skeletal muscle; small GTPase; NUCLEOTIDE-EXCHANGE FACTOR; SMALL GTPASE RAC1; GLUT4; TRANSLOCATION; PLASMA-MEMBRANE; PROTEIN-KINASE; P21-ACTIVATED KINASE; CORTICAL ACTIN; RAB PROTEINS; MICE LACKING; AS160;
D O I
10.3390/ijms151018677
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 is a hormone that regulates the blood glucose level by stimulating various physiological responses in its target tissues. In skeletal muscle and adipose tissue, insulin promotes membrane trafficking of the glucose transporter GLUT4 from GLUT4 storage vesicles to the plasma membrane, thereby facilitating the uptake of glucose from the circulation. Detailed mechanisms underlying insulin-dependent intracellular signal transduction for glucose uptake remain largely unknown. In this article, I give an overview on the recently identified signaling network involving Rab, Ras, and Rho family small guanosine triphosphatases (GTPases) that regulates glucose uptake in insulin-responsive tissues. In particular, the regulatory mechanisms for these small GTPases and the cross-talk between protein kinase and small GTPase cascades are highlighted.
引用
收藏
页码:18677 / 18692
页数:16
相关论文
共 79 条
[1]   Adipose-selective targeting of the GLUT4 gene impairs insulin action in muscle and liver [J].
Abel, ED ;
Peroni, O ;
Kim, JK ;
Kim, YB ;
Boss, O ;
Hadro, E ;
Minnemann, T ;
Shulman, GI ;
Kahn, BB .
NATURE, 2001, 409 (6821) :729-733
[2]   Identification of P-Rex1 as a Novel Rac1-Guanine Nucleotide Exchange Factor (GEF) That Promotes Actin Remodeling and GLUT4 Protein Trafficking in Adipocytes [J].
Balamatsias, Demis ;
Kong, Anne M. ;
Waters, Joanne E. ;
Sriratana, Absorn ;
Gurung, Rajendra ;
Bailey, Charles G. ;
Rasko, John E. J. ;
Tiganis, Tony ;
Macaulay, S. Lance ;
Mitchell, Christina A. .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (50) :43229-43240
[3]   Regulation of Glucose Transporter Translocation in Health and Diabetes [J].
Bogan, Jonathan S. .
ANNUAL REVIEW OF BIOCHEMISTRY, VOL 81, 2012, 81 :507-532
[4]   Insulin-responsive compartments containing GLUT4 in 3T3-L1 and CHO cells: Regulation by amino acid concentrations [J].
Bogan, JS ;
Mckee, AE ;
Lodish, HF .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (14) :4785-4806
[5]   Glucose transporter recycling in response to insulin is facilitated by myosin Myo1c [J].
Bose, A ;
Guilherme, A ;
Robida, SI ;
Nicoloro, SMC ;
Zhou, QL ;
Jiang, ZY ;
Pomerleau, DP ;
Czech, MP .
NATURE, 2002, 420 (6917) :821-824
[6]   Disruption of cortical actin in skeletal muscle demonstrates an essential role of the cytoskeleton in glucose transporter 4 translocation in insulin-sensitive tissues [J].
Brozinick, JT ;
Hawkins, ED ;
Strawbridge, AB ;
Elmendorf, JS .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (39) :40699-40706
[7]   Increased phosphorylation of Akt substrate of 160 kDa (AS160) in rat skeletal muscle in response to insulin or contractile activity [J].
Bruss, MD ;
Arias, EB ;
Lienhard, GE ;
Cartee, GD .
DIABETES, 2005, 54 (01) :41-50
[8]   Activation of RaIA is required for insulin-stimulated glut4 trafficking to the plasma membrane via the exocyst and the motor protein Myo1c [J].
Chen, Xiao-Wei ;
Leto, Dara ;
Chiang, Shian-Huey ;
Wang, Qian ;
Saltiel, Alan R. .
DEVELOPMENTAL CELL, 2007, 13 (03) :391-404
[9]   Exocyst function is regulated by effector phosphorylation [J].
Chen, Xiao-Wei ;
Leto, Dara ;
Xiao, Junyu ;
Goss, John ;
Wang, Qian ;
Shavit, Jordan A. ;
Xiong, Tingting ;
Yu, Genggeng ;
Ginsburg, David ;
Toomre, Derek ;
Xu, Zhaohui ;
Saltiel, Alan R. .
NATURE CELL BIOLOGY, 2011, 13 (05) :580-U186
[10]  
Chen Yu, 2013, Small GTPases, V4, P193, DOI 10.4161/sgtp.26471