Table 2.

IRP Activity and Ferritin Content in Monocytes From Controls and GH Patients Treated With Cytokines

Medium LPS/IFN-γ LPS/IFN-γ/NMMA SNAPLPS/IFN-γ/DFO
Control subjects (n = 16)  
 IRP (%) 100  47 ± 12* 94 ± 16  43 ± 9* 146 ± 21* 
 Ft content (ng/mg prot.) 620 ± 257  798 ± 232 667 ± 321 803 ± 221 482 ± 52 
GH patients (n = 12) 
 IRP (%)  100  93 ± 16  97 ± 14 91 ± 11  153 ± 19* 
 Ft content (ng/mg prot.) 1023 ± 627  1124 ± 735  1107 ± 642 1078 ± 756  651 ± 32* 
Medium LPS/IFN-γ LPS/IFN-γ/NMMA SNAPLPS/IFN-γ/DFO
Control subjects (n = 16)  
 IRP (%) 100  47 ± 12* 94 ± 16  43 ± 9* 146 ± 21* 
 Ft content (ng/mg prot.) 620 ± 257  798 ± 232 667 ± 321 803 ± 221 482 ± 52 
GH patients (n = 12) 
 IRP (%)  100  93 ± 16  97 ± 14 91 ± 11  153 ± 19* 
 Ft content (ng/mg prot.) 1023 ± 627  1124 ± 735  1107 ± 642 1078 ± 756  651 ± 32* 

Monocytes from control subjects and GH patients were left untreated (medium) or treated for 24 hours with 100 U/mL IFN-γ plus 1 μg/mL LPS, in the presence and absence of 0.1 mmol/L NMMA and 0.05 mmol/L Desferrioxamine (DFO). Cells were also incubated with 0.5 mmol/L SNAP for 24 hours. IRP activity was quantitated by liquid scintillation counting. Ferritin content was measured by a radioimmunoassay based on antihuman liver ferritin antibody. Values are given as mean ± SD.

*

P < .001 versus controls.

P < .05 versus controls.

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