Unidirectional transport from apical to basolateral compartment of cobalt ion in polarized Madin-Darby canine kidney cells

Biochem Biophys Res Commun. 1999 Apr 13;257(2):289-94. doi: 10.1006/bbrc.1999.0446.

Abstract

Renal transport of Co2+ was studied by use of cultured MDCK cells with cell polarity. Cells imported 57Co2+ from the apical membrane exclusively, while uptake from the basolateral membrane was minute. Apical uptake was time-, concentration-, pH-, and temperature- dependent and the dose-dependency curve was saturable, indicating that a carrier-mediated influx process operates in the apical membrane. The substrate specificity and other properties of this Co2+ transport process are distinct from those of a transporter DCT1, divalent cation transporter 1, with unusually broad substrate specificity including Co2+. Radioactive Co2+ added from the apical side appeared in the basolateral side, while there was only slight movement of Co2+ from the basolateral to apical side, indicating that this unidirectional transepithelial passage of Co2+ is not caused by the paracellular diffusion, but by the basolateral export of the cellular Co2+ uptake from the apical membrane. Our results may indicate the presence of a novel vectorial transport system responsible for the reabsorption of Co2+ from the glomerular filtrate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding, Competitive
  • Biological Transport / drug effects
  • Carrier Proteins / metabolism
  • Cation Transport Proteins*
  • Cations / metabolism*
  • Cations / pharmacology
  • Cell Line
  • Cell Membrane / metabolism
  • Cell Polarity*
  • Cobalt / metabolism*
  • Dogs
  • Dose-Response Relationship, Drug
  • Epithelial Cells / cytology
  • Epithelial Cells / drug effects
  • Epithelial Cells / metabolism
  • Hydrogen-Ion Concentration
  • Iron-Binding Proteins*
  • Kidney / cytology*
  • Kidney / drug effects
  • Kidney / metabolism
  • Membrane Proteins / metabolism
  • Metals / pharmacology
  • Sodium Azide / pharmacology
  • Substrate Specificity
  • Temperature
  • Time Factors
  • Zinc / metabolism
  • Zinc / pharmacology

Substances

  • Carrier Proteins
  • Cation Transport Proteins
  • Cations
  • Iron-Binding Proteins
  • Membrane Proteins
  • Metals
  • solute carrier family 11- (proton-coupled divalent metal ion transporters), member 2
  • Cobalt
  • Sodium Azide
  • Zinc