The Kinetics of Transferrin Endocytosis and Iron Uptake from Transferrin in Rabbit

The endocytosis of diferric transferrin and accumulation of its iron by freshly isolated rabbit reticulocytes was studied using 6sFe-'261-tran~ferrin. Internalized transferrin was distinguished from surface-bound transferrin by its resistance to release during treatment with Pronase at 4 "C. Endocytosis of diferric transferrin occurs at the same rate as exocytosis of apotransferrin, the rate constants being 0.08 min-' at 22 "C, 0.19 min-' at 30 "C, and 0.45 min" at 37 "C. At 37 "C, the maximum rate of transferrin endocytosis by reticulocytes is approximately 500 molecules/cell/s. The recycling time for transferrin bound to its receptor is about 3 min at this temperature. Neither transferrin nor its receptor is degraded during the intracellular passage. When a steady state has been reached between endocytosis and exocytosis of the ligand, about 90% of the total cell-bound transferrin is internal. Endocytosis of transferrin was found to be negligible below 10 "C. From 10 to 39 "C, the effect of temperature on the rate of endocytosis is biphasic, the rate increasing sharply above 26 "C. Over the temperature range 12-26 "C, the apparent activation energy for transferrin endocytosis is 33.0 2 2.7 kcal/mol, whereas from 26-39 "C the activation energy is considerably lower, at 12.3 f 1.6 kcal/mol. Reticulocytes accumulate iron atoms from diferric transferrin at twice the rate at which transferrin molecules are internalized, implying that iron enters the cell while still bound to transferrin. The activation energies for iron accumulation from transferrin are similar to those of endocytosis of transferrin. This study provides further evidence that transferrin-iron enters the cell by receptor-mediated endocytosis and that iron release occurs within the cell.