Endocytosis of the glucose transporter GLUT8 is mediated by interaction of a dileucine motif with the β2-adaptin subunit of the AP-2 adaptor complex

The glucose transporter GLUT8 cycles between intracellular vesicles and the plasma membrane. Like the insulin- responsive glucose transporter GLUT4, GLUT8 is primarily located in intracellular compartments under basal conditions. Whereas translocation of GLUT4 to the plasma membrane is stimulated by insulin, the distribution of GLUT8 is not affected by insulin treatment in adipose cells. However, blocking endocytosis by co- expression of a dominant-negative dynamin GTPase ( K44A) or mutation of the N-terminal dileucine (LL12/13) motif in GLUT8 leads to accumulation of the glucose transporter at the cell surface in a variety of different cell types. Yeast two-hybrid analyses and GST pulldown assays reveal that the LL signal constitutes a binding site for the beta 2-adaptin subunit of the heterotetrameric AP-2 adaptor complex, implicating this motif in targeting of GLUT8 to clathrin-coated vesicles. Moreover, yeast two-hybrid assays provide evidence that the binding site for the LL motif maps to the appendage domain of beta 2-adaptin. To analyze the biological significance of the LL/beta 2 interaction, we utilized RNA interference to specifically knockdown AP-2. Our results show that RNAi- mediated targeting of the mu 2 subunit leads to cellular depletion of AP-2, but not AP-1 adaptor complexes in HeLa cells. As a consequence, GLUT8 accumulates at the plasma membrane at comparable levels to those observed in K44A- transfected cells. Conversely, the intracellular localization of mutant GLUT8- LL/ AA is restored by replacing the LL motif in GLUT8 with the transferrin receptor- derived mu 2- adaptin binding motif YTRF, indicating that for endocytosis both AP-2 binding motifs can substitute for each other. Thus, our data demonstrate that recruitment of GLUT8 to the endocytic machinery occurs via direct interaction of the dileucine motif with beta 2- adaptin, and that endocytosis might be the main site at which GLUT8 is likely to be regulated.