Insulin increases the rate of glucose transport into fat and muscle cells b
y stimulating the translocation of intracellular Glut 4-containing vesicles
to the plasma membrane. This results in a marked increase in the amount of
the facilitative glucose transporter Glut 4 at the cell surface, allowing
for an enhanced glucose uptake. This process requires a continuous cycling
through the early endosomes, a Glut 4 specific storage compartment and the
plasma membrane. The main effect of insulin is to increase the rate of Glut
4 trafficking from its specific storage compartment to the plasma membrane.
The whole phenomenon involves signal transduction from the insulin recepto
r, vesicle trafficking (sorting and fusion processes) and actin cytoskeleto
n modifications, which are all supposed to require small GTPases. This revi
ew describes the potential role of the various members of the Ras, Rad, Rho
, Arf and Rab families in the traffic of the Glut 4-containing vesicles.