Table 2.

Summary of hepcidin derivative bioactivity



Flow cytometry

Ferritin ELISA
Peptide
Hepcidin-25 activity, %
P
Hepcidin-25 activity, %
P
Hep24   95 ± 4   .018   77 ± 19   .034  
Hep23   88 ± 4   < .001   47 ± 28   .003  
Hep22   46 ± 6   < .001   13 ± 16   < .001  
Hep21   22 ± 3   < .001   3 ± 6   < .001  
Hep20   12 ± 8   < .001   3 ± 6   < .001  
Hep3   –6 ± 10   < .001   –2 ± 10   < .001  
Hep6   1 ± 3   < .001   –5 ± 5   < .001  
Hep26   100 ± 1   NS   –   –  
delKT   90 ± 7   .01   87 ± 18   NS  
C7A/C23A   85 ± 3   < .001   107 ± 12   NS  
C11A/C19A   92 ± 6   .014   101 ± 9   NS  
C13A/C14A   92 ± 12   NS   84 ± 21   NS  
1SS   54 ± 5   < .001   36 ± 29   < .001  
G71D   108 ± 1   < .001   91 ± 11   NS  
K83R   101 ± 3   NS   107 ± 17   NS  
zebrafish   106 ± 10   NS   103 ± 8   NS  
hep25 + 20; 5 μM   102 ± 2   .05   –   –  
hep3; 20 μM   –10 ± 7   < .001   –   –  
hep25 + 3; 20 μM   102 ± 3   NS   –   –  
hep6; 20 μM   6 ± 4   < .001   –   –  
hep25 + 6; 20 μM
 
96 ± 4
 
.047
 

 

 


Flow cytometry

Ferritin ELISA
Peptide
Hepcidin-25 activity, %
P
Hepcidin-25 activity, %
P
Hep24   95 ± 4   .018   77 ± 19   .034  
Hep23   88 ± 4   < .001   47 ± 28   .003  
Hep22   46 ± 6   < .001   13 ± 16   < .001  
Hep21   22 ± 3   < .001   3 ± 6   < .001  
Hep20   12 ± 8   < .001   3 ± 6   < .001  
Hep3   –6 ± 10   < .001   –2 ± 10   < .001  
Hep6   1 ± 3   < .001   –5 ± 5   < .001  
Hep26   100 ± 1   NS   –   –  
delKT   90 ± 7   .01   87 ± 18   NS  
C7A/C23A   85 ± 3   < .001   107 ± 12   NS  
C11A/C19A   92 ± 6   .014   101 ± 9   NS  
C13A/C14A   92 ± 12   NS   84 ± 21   NS  
1SS   54 ± 5   < .001   36 ± 29   < .001  
G71D   108 ± 1   < .001   91 ± 11   NS  
K83R   101 ± 3   NS   107 ± 17   NS  
zebrafish   106 ± 10   NS   103 ± 8   NS  
hep25 + 20; 5 μM   102 ± 2   .05   –   –  
hep3; 20 μM   –10 ± 7   < .001   –   –  
hep25 + 3; 20 μM   102 ± 3   NS   –   –  
hep6; 20 μM   6 ± 4   < .001   –   –  
hep25 + 6; 20 μM
 
96 ± 4
 
.047
 

 

 

The results, expressed as percentage of the hep25 activity, are the mean ± SD of 3 to 6 independent experiments. The values obtained by flow cytometry represent the ability of peptide to cause degradation of ferroportin-GFP, and the values obtained by ferritin ELISA represent the peptides' ability to cause cellular iron retention. Each peptide was added at the concentration of 1 μM, unless indicated otherwise. Paired t test was used for statistical analysis for each peptide in comparison to hep25.

NS indicates not significant (> .05); –, not done.

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