Table 3.

Effects of Iron and Brefeldin A on Release of Ferritin from Hepatoma Cells

TreatmentDoseTotal Ferritin in Medium (μg)Inhibition by BFA (%)Total Albumin in Medium (μg)Inhibition by BFA (%)
(μg Fe/mL)
None (6) 4.3 ± 0.6  192 ± 12  
Fe-NTA (3) 10 8.5 ± 2.43-150  144 ± 43-150  
+BFA (3) 10 3.6 ± 0.13-151 58 45 ± 53-151 69 
Fe-NTA (3) 20 6.6 ± 0.73-150  135 ± 53-150  
+BFA (3) 20 3.2 ± 0.13-151 52 45 ± 13-151 67 
Imferon (3) 15 5.6 ± 0.63-150  208 ± 5  
+BFA (3) 15 3.9 ± 0.13-151 31 87 ± 33-151 59 
TreatmentDoseTotal Ferritin in Medium (μg)Inhibition by BFA (%)Total Albumin in Medium (μg)Inhibition by BFA (%)
(μg Fe/mL)
None (6) 4.3 ± 0.6  192 ± 12  
Fe-NTA (3) 10 8.5 ± 2.43-150  144 ± 43-150  
+BFA (3) 10 3.6 ± 0.13-151 58 45 ± 53-151 69 
Fe-NTA (3) 20 6.6 ± 0.73-150  135 ± 53-150  
+BFA (3) 20 3.2 ± 0.13-151 52 45 ± 13-151 67 
Imferon (3) 15 5.6 ± 0.63-150  208 ± 5  
+BFA (3) 15 3.9 ± 0.13-151 31 87 ± 33-151 59 

Conditions were the same as described in Table 2, except that the data are given as micrograms of protein per flask and that treatments were with iron, in the form of a 1:1 molar Fe(III)-nitrilotriacetate complex (Fe-NTA) or iron dextran (Imferon), ± brefeldin A (BFA) (4 μg/mL). Values are means ± SD (for the number of flasks indicated in parentheses). There was no significant effect of any of the treatments on cell growth or viability, as determined by the amounts of cell protein per flask.

F3-150

P < .05 to P < .001 for difference from controls.

F3-151

Significant inhibition by BFA (P < .001).

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