Figure 4.
Figure 4. TfR2 protein levels in genetic models of hepatic iron loading. Hepatic tissue was obtained for 3 different mouse models: 10-week-old Hfe-/- mice, a genetic model of human hereditary iron overload due to loss of Hfe function, 4- to 5-week old Trfhpx/hpx mice, which have impaired Tf synthesis, and 6-week-old Hbbth-1 mice, which have defective globin synthesis. Controls for the latter group included 2 wild-type and 2 heterozygous HRI+/- mice that were both Hbbwt; all Hbbth-1 mice were wild type for HRI.29 After Western analysis, TfR2 protein levels were determined by densitometry using Quantity One software (Bio-Rad) to compare expression levels; shown are mean values (± SEM) normalized to actin (loading control). The numbers of mice for each group are noted in the figure. *different from control, P < .05. The increase in TfR2 levels determined for Hfe-/- mice may be an underestimate because a small increase in actin levels was noted for these animals.

TfR2 protein levels in genetic models of hepatic iron loading. Hepatic tissue was obtained for 3 different mouse models: 10-week-old Hfe-/- mice, a genetic model of human hereditary iron overload due to loss of Hfe function, 4- to 5-week old Trfhpx/hpx mice, which have impaired Tf synthesis, and 6-week-old Hbbth-1 mice, which have defective globin synthesis. Controls for the latter group included 2 wild-type and 2 heterozygous HRI+/- mice that were both Hbbwt; all Hbbth-1 mice were wild type for HRI.29  After Western analysis, TfR2 protein levels were determined by densitometry using Quantity One software (Bio-Rad) to compare expression levels; shown are mean values (± SEM) normalized to actin (loading control). The numbers of mice for each group are noted in the figure. *different from control, P < .05. The increase in TfR2 levels determined for Hfe-/- mice may be an underestimate because a small increase in actin levels was noted for these animals.

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