Article Text
Review
Molecular pathogenesis of iron overload
Abstract
Our current understanding of iron absorption under normal conditions is presented, together with an overview of the clinical disorders of iron overload and the molecular processes that contribute to increased iron deposition in iron overload. Recently, a number of new genes involved in iron metabolism have been identified which is allowing the molecular mechanisms of iron absorption to be elucidated.
- divalent metal transporter 1
- ferroportin
- iron regulating elements
- haemochromatosis
- haephestin
- hepcidin
- iron
- DMT1, divalent metal transporter 1
- HFE, haemochromatosis protein
- HH, hereditary haemochromatosis
- IRE, iron regulatory element
- IRP, iron regulatory protein
- NTBI, non-transferrin bound iron
- TBI, transferrin bound iron
- TfR1, transferrin receptor 1
- TfR2, transferrin receptor 2