Abstract

The present study investigated the mechanisms of intestinal cadmium (Cd) uptake and efflux, using isolated enterocytes of freshwater rainbow trout (Oncorhynchus mykiss) as the experimental model. The apical uptake of free Cd2+ in the enterocytes was a saturable and high-affinity transport process. Both zinc (Zn2+) and iron (Fe2+) inhibited cellular Cd2+ uptake through a competitive interaction, suggesting that Cd2+ enters enterocytes via both Zn2+ (e.g., ZIP8) and Fe2+ (e.g., DMT1) transport pathways. Cellular Cd2+ uptake increased in the presence of HCO3−, which resembled the function of mammalian ZIP8. Cellular Cd2+ uptake was unaffected by Ca2+, indicating that Cd2+ does not compete with Ca2+ for apical uptake. Interestingly, Cd uptake was influenced by the presence of l-cysteine, and under the exposure condition where Cd(Cys)+ was the predominant Cd species, cellular Cd uptake rate increased with the increased concentration of Cd(Cys)+. The kinetic analysis indicated that the uptake of Cd(Cys)+ occurs through a low capacity transport mechanism relative to that of free Cd2+. In addition, Cd efflux from the enterocytes decreased in the presence of an ATPase inhibitor (orthovanadate), suggesting the existence of an ATPase-coupled extrusion process. Overall, our findings provide new mechanistic insights into the intestinal Cd transport in freshwater fish.

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