Iron uptake by rabbit intestinal brush border membrane vesicles involves movement through the outer surface, membrane interior, inner surface and aqueous interior.

Abstract

Iron uptake in rabbit brush border membrane vesicles was measured in the presence of nitrilotriacetate. The complexes formed ranged from stable mononuclear species to hydrolyzed polynuclear complexes and are considered as a good model for nutritional iron compounds with respect to their chemical reactivity. Uptake includes both binding to and penetration through the membrane. A strategy was developed to localize iron in the following four compartments: outer membrane surface, membrane interior, inner membrane surface and aqueous phase within the vesicles. Both surfaces as well as the membrane interior revealed a high metal binding capacity. After an incubation for 10 min with 182 mumol/L iron and 364 mumol/L nitrilotriacetate, 35% of total vesicle iron was found to be bound to the outer membrane surface, 34% to the inner membrane surface, and 23% was not accessible to EDTA. Thus, by adsorption of polynuclear iron complexes to the outer surface, the residence time of iron may be prolonged. The remaining 8% of total iron was in the aqueous phase within the vesicles. Nitrilotriacetate enters the rabbit vesicles in a concentration-dependent manner. As a consequence, iron concentration in the aqueous phase within the vesicles will be driven to the medium equilibrium concentration.