Biotin uptake mechanisms in brush-border and basolateral membrane vesicles isolated from rabbit kidney cortex

Biochim Biophys Acta. 1986 Apr 25;856(3):471-81. doi: 10.1016/0005-2736(86)90138-0.

Abstract

Biotin transport was studied using brush-border and basolateral membrane vesicles isolated from rabbit kidney cortex. An inwardly directed Na+ gradient stimulated biotin uptake into brush-border membrane vesicles and a transient accumulation of the anion against its concentration gradient was observed. In contrast, uptake of biotin by basolateral membrane vesicles was found to be Na+-gradient insensitive. Generation of a negative intravesicular potential by valinomycin-induced K+ diffusion potentials or by the presence of Na+ salts of anions of different permeabilities enhanced biotin uptake by brush-border membrane vesicles, suggesting an electrogenic mechanism. The Na+ gradient-dependent uptake of biotin into brush-border membrane vesicles was saturable with an apparent Km of 28 microM. The Na+-dependent uptake of tracer biotin was significantly inhibited by 50 microM biotin, and thioctic acid but not by 50 microM L-lactate, D-glucose, or succinate. Finally, the existence in both types of membrane vesicles of a H+/biotin- cotransport system could not be demonstrated. These results are consistent with a model for biotin reabsorption in which the Na+/biotin- cotransporter in luminal membranes provides the driving force for uphill transport of this vitamin.

MeSH terms

  • Animals
  • Biological Transport / drug effects
  • Biotin / metabolism*
  • Cell Membrane / metabolism
  • Glucose / pharmacology
  • Hydrogen-Ion Concentration
  • In Vitro Techniques
  • Kidney Cortex / metabolism*
  • Membrane Potentials
  • Microvilli / metabolism
  • Osmotic Pressure
  • Potassium Chloride / pharmacology
  • Rabbits
  • Sodium / metabolism
  • Sodium / pharmacology
  • Valinomycin / pharmacology

Substances

  • Valinomycin
  • Potassium Chloride
  • Biotin
  • Sodium
  • Glucose