Clinical, pathological, and molecular correlates in ferroportin disease: a study of two novel mutations.

Abstract

BACKGROUND/AIMS:

Clinico-pathological manifestations of ferroportin (Fpn) disease (FD) are heterogeneous, with some patients presenting with iron overload predominantly in macrophages ("M" phenotype), others predominantly in hepatocytes ("H" phenotype). This appears to reflect functional heterogeneity of Fpn mutants, with loss-of-function generally resulting in the M type.

METHODS:

Two unrelated probands with "non-HFE" hemochromatosis were screened for Fpn mutations. Mutants were functionally characterized by immunofluorescence microscopy, evaluation of their ability to bind hepcidin and export iron, and by expressing them in zebrafish.

RESULTS:

Two novel Fpn mutations were identified: I152F in patient-1, presenting with typical M phenotype; and L233P in patient-2, presenting with ambiguous features (massive overload in both macrophages and hepatocytes). Molecular studies suggested loss of function in both cases. The I152F, normally localized on cell membrane and internalized by hepcidin, showed a unique "primary" deficit of iron export capability. The L233P did not appropriately traffic to cell surface. Loss of function was confirmed by expressing both mutants in vivo in zebrafish, resulting in iron limited erythropoiesis. Clinical manifestations were likely enhanced in both patients by non-genetic factors (HCV, alcohol).

CONCLUSIONS:

The combination of careful review of clinico-pathological data with molecular studies can yield compelling explanations for phenotype heterogeneity in FD.

• Authors: Domenico Girelli, Ivana De Domenico, Claudia Bozzini, Natascia Campostrini, Fabiana Busti, Annalisa Castagna, Nadia Soriani, Laura Cremonesi, Maurizio Ferrari, Romano Colombari, Diane McVey Ward, Jerry Kaplan, Roberto Corrocher
• Journal: Journal of hepatology (J Hepatol) Vol. 49 Issue 4 Pg. 664-71 (Oct 2008) ISSN: 0168-8278 [Print] Netherlands
• PMID: 18713659 (Publication Type: Case Reports, Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)

Chemical References

• Antimicrobial Cationic Peptides
• Cation Transport Proteins
• HAMP protein, human
• Hepcidins
• metal transporting protein 1
• Iron

Topics

• Animals
• Antimicrobial Cationic Peptides (metabolism)
• Biopsy
• Cation Transport Proteins (genetics)
• Female
• Hemochromatosis (genetics, metabolism, pathology)
• Hepcidins
• Humans
• Iron (metabolism)
• Liver (pathology)
• Male
• Middle Aged
• Mutation (genetics)
• Pedigree
• Zebrafish