Iron is required for cellular life. However, abnormalities of its metabolis
m may lead to iron deficiency or iron overload both conditions which are de
leterious. Therefore, stock and distribution of iron in the body must be ve
ry stable. Classically, four major proteins are involved in iron metabolism
: (a) transferrin which is implicated in its plasmatic transport, (b) tran
sferrin receptor which regulates iron-transferrin uptake, (c) ferritin, the
major iron storage protein, and (d) IRP (Iron Regulatory Protein) which re
gulates both the entry and storage of iron by linking to the IRE (Iron Resp
onsive Element), a nucleotidic sequence found on transferrin receptor and f
erritin mRNA. Thus, IRP adapts gene expression to the iron cellular status.
Recent data give informations about new proteins involved in iron metaboli
sm: HFE whose gene is mutated in genetic hemochromatosis, ceruloplasmin whi
ch permits cellular iron egress and frataxin which is implicated in the exi
t of iron from mitochondria.