Expression of a human renal sodium nucleoside cotransporter in Xenopus laevis oocytes

Biochem Pharmacol. 1994 Dec 16;48(12):2251-3. doi: 10.1016/0006-2952(94)00411-0.

Abstract

In this study, Xenopus laevis oocytes injected with poly(A)+ RNA (mRNA) isolated from human kidney were used to express a Na(+)-nucleoside cotransporter. Na(+)-stimulated [3H]thymidine uptake was enhanced 2-3-fold in oocytes injected with 50 ng poly(A)+ RNA and 4-5-fold in oocytes injected with 20 ng of a size-fractionated human renal cortex mRNA fragment (2-3 kb) in comparison with water-injected oocytes. Na(+)-dependent thymidine uptake in oocytes injected with the 2-3 kb mRNA fragment was inhibited significantly by thymidine and guanosine but not by formycin B, consistent with the N4 Na(+)-nucleoside cotransporter. The Km (28 microM) of Na(+)-dependent thymidine uptake in the oocytes injected with the 2-3 kb mRNA fragment was similar to the Km (27 microM) of Na(+)-dependent thymidine uptake obtained in human renal brush border membrane vesicles. These data suggest for the first time that a Na(+)-nucleoside cotransporter from human kidney can be expressed in X. laevis oocytes.

Publication types

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

MeSH terms

  • Animals
  • Carrier Proteins / genetics*
  • Gene Expression
  • Humans
  • Kidney / metabolism*
  • Kinetics
  • Nucleosides / metabolism
  • Oocytes / metabolism*
  • RNA, Messenger / pharmacology
  • Sodium / metabolism
  • Symporters*
  • Transfection
  • Xenopus laevis

Substances

  • Carrier Proteins
  • Nucleosides
  • RNA, Messenger
  • Symporters
  • sodium-nucleoside cotransporter
  • Sodium