Figure 2.
Figure 2. Heph and Ireg1 expression is responsive to systemic rather than local iron levels. (A) Northern blot analysis of enterocytes from sla mice fed control diet (sla) and C57BL/6J mice fed control (Ctrl), iron-deficient (Fe–), or iron-overload (Fe+) diets for 6 months. Blots were sequentially hybridized to probes for Heph, Ireg1, TfR, and Dmt1. The 18S rRNA band was used as a loading control. (B) Relative mRNA levels of Heph, Ireg1, TfR1, and Dmt1 were quantified using NIH Image and densitometry values normalized to values obtained for 18S. Data are means ± SD as percent control from 5 independent experiments. *P < .05 versus control.

Heph and Ireg1 expression is responsive to systemic rather than local iron levels. (A) Northern blot analysis of enterocytes from sla mice fed control diet (sla) and C57BL/6J mice fed control (Ctrl), iron-deficient (Fe), or iron-overload (Fe+) diets for 6 months. Blots were sequentially hybridized to probes for Heph, Ireg1, TfR, and Dmt1. The 18S rRNA band was used as a loading control. (B) Relative mRNA levels of Heph, Ireg1, TfR1, and Dmt1 were quantified using NIH Image and densitometry values normalized to values obtained for 18S. Data are means ± SD as percent control from 5 independent experiments. *P < .05 versus control.

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