Fig. 4.
Fig. 4. The regulated iron uptake from transferrin is HFE-expression–dependent. HtTA cells (•) and HtTA-HFE cells (○) were grown in the absence of doxycycline. Cells were divided and either left untreated or doxycycline (1 μg/mL) was added. At different times after onset of doxycycline-mediated HFE repression, iron uptake was examined in doxycycline-treated and untreated cells. Uptake was determined for 30 minutes at 37°C with 5 μg/mL59Fe-diferric transferrin as substrate. The results are given as quotient of uptake rates of doxycyline treated vuntreated cells. All data are derived from triplicate samples.

The regulated iron uptake from transferrin is HFE-expression–dependent. HtTA cells (•) and HtTA-HFE cells (○) were grown in the absence of doxycycline. Cells were divided and either left untreated or doxycycline (1 μg/mL) was added. At different times after onset of doxycycline-mediated HFE repression, iron uptake was examined in doxycycline-treated and untreated cells. Uptake was determined for 30 minutes at 37°C with 5 μg/mL59Fe-diferric transferrin as substrate. The results are given as quotient of uptake rates of doxycyline treated vuntreated cells. All data are derived from triplicate samples.

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