Fig. 9.
Fig. 9. (A) Internalization of 125I-Tf by cells. Cells were incubated with 125I-Tf at 4°C to allow for ligand binding to cell surface TfRs. Cells were washed to remove unbound 125I-Tf and incubated at 37°C to allow for internalization of 125I-Tf. At the specified times, aliquots of cells were removed and centrifuged through an acidic buffer to determine the fraction of 125I-Tf internalized. Data shown are representative of three separate experiments. (•) S; (00) R1; (▵) R2 cells. (B) Release of 125I-Tf from cells. Cells were allowed to incorporate 125I-Tf at 37°C, washed to remove unincorporated radioactivity, and then incubated in serum-free medium containing 100 μg/mL Tf-Fe (nonradioactive). The amount of 125I-Tf released by cells at the specified times was determined as described the text. (•) S; (00) R1 cells. Data represent means ± SE (n = 3). Differences between S and R1 cells after the 5-minute time point are significant (P < .004).

(A) Internalization of 125I-Tf by cells. Cells were incubated with 125I-Tf at 4°C to allow for ligand binding to cell surface TfRs. Cells were washed to remove unbound 125I-Tf and incubated at 37°C to allow for internalization of 125I-Tf. At the specified times, aliquots of cells were removed and centrifuged through an acidic buffer to determine the fraction of 125I-Tf internalized. Data shown are representative of three separate experiments. (•) S; (00) R1; (▵) R2 cells. (B) Release of 125I-Tf from cells. Cells were allowed to incorporate 125I-Tf at 37°C, washed to remove unincorporated radioactivity, and then incubated in serum-free medium containing 100 μg/mL Tf-Fe (nonradioactive). The amount of 125I-Tf released by cells at the specified times was determined as described the text. (•) S; (00) R1 cells. Data represent means ± SE (n = 3). Differences between S and R1 cells after the 5-minute time point are significant (P < .004).

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