Sodium-dependent, concentrative nucleoside transport in Walker 256 rat carcinosarcoma cells

Biochem Biophys Res Commun. 1991 Mar 29;175(3):846-51. doi: 10.1016/0006-291x(91)91642-p.

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 microM 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 nucleoside transporter. The specificity of this transporter appears to correspond to one of the two Na(+)-dependent transporters previously described in mouse intestinal epithelial cells.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Biological Transport / drug effects
  • Carcinoma 256, Walker / metabolism*
  • Dipyridamole / pharmacology
  • Formycins / metabolism*
  • Inosine / metabolism
  • Kinetics
  • Nucleosides / metabolism*
  • Rats
  • Sodium / pharmacology*
  • Thymidine / metabolism
  • Uridine / metabolism

Substances

  • Formycins
  • Nucleosides
  • formycin B
  • Inosine
  • Dipyridamole
  • Sodium
  • Thymidine
  • Uridine