Waterborne iron accumulation by the gills of the zebrafish Danio rerio was assessed in ion-poor water. Branchial iron uptake, which comprises both the iron that has entered the gill cells and iron that is strongly bound to the epithelia, has high- and low-affinity components. At low nominal [Fe] (<40 nmol l-1) the high-affinity component demonstrated saturation kinetics, with an apparent Km of 5.9 nmol l-1 Fe and Vmax of 2.1 pmol g-1 h-1. Over a range of higher nominal [Fe] (40-200 nmol l-1), branchial uptake was linear. In the presence of 2μmol l-1 of the reducing agent dithiothreitol (DTT), branchial iron accumulation was significantly enhanced at [Fe]>15 nmol l-1. The proton pump inhibitor bafilomycin A significantly reduced iron uptake in the presence of DTT. On the basis of these observations we conclude that branchial iron uptake at low [Fe] shows characteristics similar to those of other iron-transporting epithelia, coupling an apical membrane ferric reductase to a Fe2+/H+ symporter. Zebrafish branchial iron transport at 18.6 nmol l-1 was inhibited by 200 nmol l-1 Cd2+. But, unlike other Fe2+/H+ symporters, iron uptake was not affected by other divalent metals (Co2+, Ni2+, Pb2+,Cu2+, Zn2+ and Mn2+). Zebrafish loaded with 59Fe from the water showed a loss of 7.9 pmol Fe g-1body mass over the first day and a further loss of 5.7 pmol Fe g-1body mass over the following 28 days. The depuration kinetics followed a two-component exponential model; for the short-lived component, t1/2=0.31 days, and for the long-lived component, t1/2=13.2 days. The daily iron loss by zebrafish can be compensated by iron uptake at exceedingly low water iron concentrations(uptake rate at 1.625 nmol l-1 Fe=0.425 pmol g-1h-1), demonstrating that uptake of iron from the water is potentially an important source of this nutritive metal in freshwater teleost fish.

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