Figure 7.
Ablation of intestinal DMT1 abolished the increase in iron flux induced by exposure to the 4 AA formulation. Duodenal epithelial tissues isolated from DMT1 intestine-specific knockout (DMT1int/int) mice were mounted in Ussing chambers and bathed in control or 4 AA formulations. Tissues were paired based on conductance, 15 µCi of 59Fe was added to one side of the chamber, and samples were acquired every 15 minutes from the other side for 1 hour. Jnet was calculated by subtracting Jsm from Jms. No significant difference was observed with respect to 59Fe flux (A) (n = 3-6 per group for Jnet) or conductance (B) (n = 6 to 12 per group) in the presence of the control or 4 AA formulations. Data were analyzed by Student’s t test for each sex and at each time point for conductance.

Ablation of intestinal DMT1 abolished the increase in iron flux induced by exposure to the 4 AA formulation. Duodenal epithelial tissues isolated from DMT1 intestine-specific knockout (DMT1int/int) mice were mounted in Ussing chambers and bathed in control or 4 AA formulations. Tissues were paired based on conductance, 15 µCi of 59Fe was added to one side of the chamber, and samples were acquired every 15 minutes from the other side for 1 hour. Jnet was calculated by subtracting Jsm from Jms. No significant difference was observed with respect to 59Fe flux (A) (n = 3-6 per group for Jnet) or conductance (B) (n = 6 to 12 per group) in the presence of the control or 4 AA formulations. Data were analyzed by Student’s t test for each sex and at each time point for conductance.

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