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(Received for publication, January 24, 1997, and in revised form, April 7, 1997)
From Departamento de Biología, Facultad de Ciencias,
Universidad de Chile, Casilla 653, Santiago, Chile and
§ Department of Medicine, Louisiana State University Medical
Center at Shreveport, Shreveport, Louisiana 71130
Previous studies have demonstrated that diferric
transferrin and apotransferrin compete for the binding to basolateral
transferrin receptors and that transferrin-mediated iron uptake by
Caco-2 cells is inhibited by apotransferrin to a larger extent than
that predicted solely by receptor competition. This inhibition can have
important implications in determining the net exchange of iron between
intestinal cells and the basolateral milieu. Accordingly, we further
characterized the endocytic cycles of apotransferrin and diferric
transferrin in Caco-2 cells. We found that after internalization both
apotransferrin and diferric transferrin recycled to the cell exterior,
but that apotransferrin had a protracted endocytic cycle. Confocal
microscopy studies revealed a different cellular distribution of
apotransferrin and diferric transferrin; both were found in a
compartment close to the basal membrane, but apotransferrin reached as
well regions closer to the apical membrane. Moreover, the intracellular
distribution of transferrin receptors was influenced by the iron load
of transferrin; cells incubated with apotransferrin presented a more
apical distribution of transferrin receptors than cells incubated with
diferric transferrin. These results indicate for the first time that
the endocytic cycle of transferrin receptors in intestinal epithelial
cells is determined by the iron content of transferrin. They explain
also the marked inhibitory effect of apotransferrin on
transferrin-mediated iron uptake by Caco-2 cells, since incubation of
cells with apotransferrin resulted in the actual sequestration of the
receptor in the cell interior.
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