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

被引:90
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
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
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