The rate of iron release from HepG2 liver cells was increased not only
by extracellular apotransferrin, but also by diferric transferrin, in
a non-additive, concentration-dependent manner and to a similar magni
tude. This suggests that rapid equilibration between receptor-mediated
uptake and the release process determines net iron retention by the l
iver, Release was also accelerated by ceruloplasmin; most importantly,
the effect of this protein was greatest when iron release was occurri
ng rapidly, stimulated by apotransferrin, or under conditions of Limit
ed oxygen. Thus iron release involves both apotransferrin and ferrotra
nsferrin, with ceruloplasmin playing a role in tissues with limited ox
ygen supply, as in the liver in vivo. (C) 1997 Federation of European
Biochemical Societies.