Functional characterization of albumin binding to the apical membrane of OK cells

Am J Physiol. 1996 Aug;271(2 Pt 2):F286-91. doi: 10.1152/ajprenal.1996.271.2.F286.

Abstract

We characterized binding of albumin to the apical membrane of opossum kidney (OK) cells using fluorescein isothiocyanate (FITC)-albumin (i.e., bovine serum albumin, BSA) as substrate. Functional analysis of binding data showed one specific binding site characterized by half-maximal binding (Michaelis constant, (Km) at 20 mg/l (300 nmol/l) and maximal binding capacity (Bmax) of 0.61 microgram/mg cellular protein. Excess of unlabeled albumin (BSA) inhibited binding at low concentrations of FITC-albumin completely but only partially at high concentrations. FITC-albumin binding was reversible and pH dependent. Km increased about sixfold when pH decreased from 7.4 to 5.0. The inhibitory effects of conalbumin, alpha-lactalbumin, and transferrin were significantly smaller compared with BSA. We conclude that OK cells express a high-affinity binding site for albumin on the apical membrane. This binding site is pH sensitive, binds albumin in the physiological range, and could be responsible for the effective receptor-mediated reabsorption of albumin in the proximal tubule.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Line
  • Cell Membrane / metabolism
  • Fluorescein-5-isothiocyanate / analogs & derivatives
  • Fluorescein-5-isothiocyanate / metabolism
  • Hydrogen-Ion Concentration
  • Kidney / cytology
  • Kidney / metabolism*
  • Kinetics
  • Opossums
  • Serum Albumin, Bovine / metabolism*
  • Serum Albumin, Bovine / pharmacology

Substances

  • fluorescein isothiocyanate bovine serum albumin
  • Serum Albumin, Bovine
  • Fluorescein-5-isothiocyanate