Sodium-dependent, concentrative nucleoside transport in Walker 256 rat carcinosarcoma cells
Abstract
Nucleoside transport in Walker 256 cells was reexamined using formycin B, a nonmetabolized analog of inosine. In the presence of dipyridamole to inhibit the equilibrative (facilitated diffusion) transporter previously described in these cells, the initial rate of uptake of 1 μM formycin B was 10-fold greater in Na+-containing medium than in Na+-free medium. In the presence of Na+ and dipyridamole the intracellular concentration of formycin B exceeded that in the medium within one min and was 6-fold greater than that of the medium by 5 min. Na+-dependent transport of formycin B was inhibited by low concentrations of inosine, but not thymidine. Furthermore, Na+-dependent transport of uridine, but not thymidine, was apparent in the presence of dipyridamole. These data indicate that Walker 256 cells have, in addition to the previously described equilibrative transporter, a concentrative mucleoside transporter. The specificity of this transporter appears to correspond to one of the two Na+-dependent transporters previously described in mouse intestinal epithelial cells. © 1991.
Publication Title
Biochemical and Biophysical Research Communications
Recommended Citation
Crawford, C., & Belt, J. (1991). Sodium-dependent, concentrative nucleoside transport in Walker 256 rat carcinosarcoma cells. Biochemical and Biophysical Research Communications, 175 (3), 846-851. https://doi.org/10.1016/0006-291X(91)91642-P
