Expression of rat renal sulfate transport systems in Xenopus laevis oocytes. Functional characterization and molecular identification

J Biol Chem. 1994 Jan 28;269(4):3022-6.

Abstract

Renal proximal tubular sulfate reabsorption is mediated by brush border membrane Na+/sulfate-cotransport and basolateral Na(+)-independent sulfate transport. Injection of rat kidney cortex mRNA into Xenopus laevis oocytes induced Na(+)-dependent as well as Na(+)-independent sulfate transport. The inhibition pattern of Na(+)-dependent uptake coincided with that known for the brush border membrane; the inhibition pattern of Na(+)-independent uptake suggested that this activity could be related to the basolateral cell surface. By Northern blot hybridization of size-fractionated mRNA, we provide evidence that the Na(+)-dependent uptake is induced by an mRNA species related to a recently cloned cDNA encoding rat renal cortex Na+/SO4 cotransport (NaSi-1; Markovich, D., Forgo, J., Stange, G., Biber, J., and Murer, H. (1993) Proc. Natl. Acad. Sci. U.S.A. 90, 8073-8077); the Na(+)-independent sulfate transport activity seems to be related to an mRNA species encoding a rat liver Na(+)-independent sulfate transporter (Bissig, M., Hagenbuch, B., Stieger, B., Koller, T., and Meier, P. J. (1994) J. Biol. Chem. 269, 3017-3021). Hybrid depletion experiments using antisense oligonucleotides provided further evidence for the association of the expressed transport activities to NaSi-1 and sat-1, respectively.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid / pharmacology
  • Animals
  • Base Sequence
  • Biological Transport, Active / drug effects
  • Carrier Proteins / biosynthesis*
  • Carrier Proteins / metabolism
  • Female
  • Kidney Cortex / metabolism*
  • Kinetics
  • Membrane Transport Proteins*
  • Microvilli / metabolism
  • Molecular Sequence Data
  • Oligodeoxyribonucleotides
  • Oligonucleotides, Antisense
  • RNA, Messenger / metabolism
  • Rats
  • Sodium / metabolism
  • Sulfate Transporters
  • Sulfates / metabolism*
  • Thiosulfates / pharmacology
  • Xenopus laevis

Substances

  • Carrier Proteins
  • Membrane Transport Proteins
  • Oligodeoxyribonucleotides
  • Oligonucleotides, Antisense
  • RNA, Messenger
  • SLC26A4 protein, human
  • Sulfate Transporters
  • Sulfates
  • Thiosulfates
  • Sodium
  • 4,4'-Diisothiocyanostilbene-2,2'-Disulfonic Acid