Endocytosis, Recycling, and Regulated Exocytosis of Glucose Transporter 4

被引:123
作者
Foley, Kevin [1 ,2 ]
Boguslavsky, Shlomit [1 ]
Klip, Amira [1 ,2 ]
机构
[1] Hosp Sick Children, Cell Biol Program, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Dept Biochem, Toronto, ON, Canada
关键词
STIMULATED GLUT4 TRANSLOCATION; PROTEIN-KINASE-C; GTPASE-ACTIVATING PROTEIN; RESPONSIVE STORAGE COMPARTMENT; GUANINE-NUCLEOTIDE EXCHANGE; INDUCED INSULIN-RESISTANCE; NEWLY SYNTHESIZED GLUT4; HEAVY-CHAIN ISOFORM; RAT SKELETAL-MUSCLE; GLUCOSE-TRANSPORT;
D O I
10.1021/bi2000356
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
Glucose transporter 4 (GLUT4) is responsible for the uptake of glucose into muscle and adipose tissues. Under resting conditions, GLUT4 is dynamically retained through idle cycling among selective intracellular compartments, from whence it undergoes slow recycling to the plasma membrane (PM). This dynamic retention can be released by command from intracellular signals elicited by insulin and other stimuli, which result in 2-10-fold increases in the surface level of GLUT4. Insulin-derived signals promote translocation of GLUT4 to the PM from a specialized compartment termed GLUT4 storage vesicles (GSV). Much effort has been devoted to the characterization of the intracellular compartments and dynamics of GLUT4 cycling and to the Signals by which GLUT4 is sorted into, and recruited from, GSV. This review summarizes our understanding of intracellular GLUT4 traffic during its internalization from the membrane, its slow, constitutive recycling, and its regulated exocytosis in response to insulin. In spite of specific differences in GLUT4 dynamic behavior in adipose and muscle cells, the generalities of its endocytic and exocytic itineraries are consistent and an array of regulatory proteins that regulate each vesicular traffic event emerges from these cell systems.
引用
收藏
页码:3048 / 3061
页数:14
相关论文
共 172 条
[1]   Disruption of microtubules in rat skeletal muscle does not inhibit insulin- or contraction-stimulated glucose transport [J].
Ai, H ;
Ralston, E ;
Lauritzen, HPMM ;
Galbo, H ;
Ploug, T .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2003, 285 (04) :E836-E844
[2]  
Al-Hasani H, 2002, J CELL SCI, V115, P131
[3]   Identification and characterization of two distinct intracellular GLUT4 pools in rat skeletal muscle: evidence for an endosomal and an insulin-sensitive GLUT4 compartment [J].
Aledo, JC ;
Lavoie, L ;
Volchuk, A ;
Keller, SR ;
Klip, A ;
Hundal, HS .
BIOCHEMICAL JOURNAL, 1997, 325 :727-732
[4]   Clathrin-dependent and independent endocytosis of glucose transporter 4 (GLUT4) in myoblasts:: Regulation by mitochondrial uncoupling [J].
Antonescu, Costin N. ;
Diaz, Monica ;
Femia, Guiseppe ;
Planas, Josep V. ;
Klip, Amira .
TRAFFIC, 2008, 9 (07) :1173-1190
[5]   Ready, set, internalize: mechanisms and regulation of GLUT4 endocytosis [J].
Antonescu, Costin N. ;
Foti, Michelangelo ;
Sauvonnet, Nathalie ;
Klip, Amira .
BIOSCIENCE REPORTS, 2009, 29 (01) :1-11
[6]   Functional role of sortilin in myogenesis and development of insulin-responsive glucose transport system in C2C12 myocytes [J].
Ariga, Miyako ;
Nedachi, Taku ;
Katagiri, Hideki ;
Kanzaki, Makoto .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (15) :10208-10220
[7]   Dissecting multiple steps of GLUT4 trafficking and identifying the sites of insulin action [J].
Bai, Li ;
Wang, Yan ;
Fan, Junmei ;
Chen, Yu ;
Ji, Wei ;
Qu, Anlian ;
Xu, Pingyong ;
James, David E. ;
Xu, Tao .
CELL METABOLISM, 2007, 5 (01) :47-57
[8]   Snapin interacts with the exo70 subunit of the exocyst and modulates GLUT4 trafficking [J].
Bao, Yiqun ;
Lopez, Jamie A. ;
James, David E. ;
Hunziker, Walter .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (01) :324-331
[9]   A dual role of the N-terminal FQQI motif in GLUT4 trafficking [J].
Bernhardt, Ulrike ;
Carlotti, Francoise ;
Hoeben, Rob C. ;
Joost, Hans-Georg ;
Al-Hasani, Hadi .
BIOLOGICAL CHEMISTRY, 2009, 390 (09) :883-892
[10]   Brought in by force: AMPK, TBC1D1, and contraction-stimulated glucose transport in skeletal muscle [J].
Bilan, Philip J. ;
Schertzer, Jonathan D. .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2009, 296 (05) :E965-E966