Effects of various metal ions on the gene expression of iron exporter ferroportin-1 in J774 macrophages.
- Author:
Bo Yeon PARK
1
;
Jayong CHUNG
Author Information
- Publication Type:Brief Communication
- Keywords: Ferroportin-1; divalent metals; copper; macrophages; iron export
- MeSH: Blotting, Western; Cobalt; Copper; Gene Expression; Ions; Iron; Luciferases; Macrophages; Manganese; Metals; Real-Time Polymerase Chain Reaction; Recycling; RNA, Messenger; Zinc
- From:Nutrition Research and Practice 2008;2(4):317-321
- CountryRepublic of Korea
- Language:English
- Abstract: Macrophages play a key role in iron metabolism by recycling iron through erythrophagocytosis. Ferroportin-1 (FPN1) is a transporter protein that is known to mediate iron export from macrophages. Since divalent metals often interact with iron metabolism, we examined if divalent metals could regulate the expression of FPN1 in macrophages. J774 macrophage cells were treated with copper, manganese, zinc, or cobalt at 10, 50, or 100 microM for 16 to 24 h. Then, FPN1 mRNA and protein levels were determined by quantitative real-time PCR and Western blot analyses, respectively. In addition, effects of divalent metals on FPN1 promoter activity were examined by luciferase reporter assays. Results showed that copper significantly increased FPN1 mRNA levels in a dose-dependent manner. The copper-induced expression of FPN1 mRNA was associated with a corresponding increase in FPN1 protein levels. Also, copper directly stimulated the activity of FPN1 promoter-driven reporter construct. In contrast, manganese and zinc had no effect on the FPN1 gene expression in J774 cells. Interestingly, cobalt treatment in J774 cells decreased FPN1 protein levels without affecting FPN1 mRNA levels. In conclusion, our study results demonstrate that divalent metals differentially regulate FPN1 expression in macrophages and indicate a potential interaction of divalent metals with the FPN1-mediated iron export in macrophages.
