W. Breuer et al., IRON ACQUIRED FROM TRANSFERRIN BY K562 CELLS IS DELIVERED INTO A CYTOPLASMIC POOL OF CHELATABLE IRON(II), The Journal of biological chemistry, 270(41), 1995, pp. 24209-24215
The release of iron from transferrin (Tf) in the acidic milieu of endo
somes and its translocation into the cytosol are integral steps in the
process of iron acquisition via receptor-mediated endocytosis (RME),
The translocated metal is thought to enter a low molecular weight cyto
plasmic pool, presumed to contain the form of iron which is apparently
sensed by iron responsive proteins and is the direct target of iron c
helators, The process of iron delivery into the cytoplasmic chelatable
pool of K562 cells was studied in situ by continuous monitoring of th
e fluorescence of cells loaded with the metal-sensitive probe calcein,
Upon exposure to Tf at 37 degrees C, intracellular fluorescence decay
ed, corresponding to an initial iron uptake of 40 nM/min, The Tf-media
ted iron uptake was profoundly inhibited by weak, bases, the protonoph
ore monensin, energy depletion, or low temperatures (<25 degrees C), a
ll properties characteristic of RME, Cell iron levels were affected by
the slowly permeating chelator desferrioxamine only after prolonged i
ncubations, Conversely, rapidly penetrating, lipophilic iron(II) chela
tors such as 2,2'-bipyridyl, evoked swift increases in cell calcein fl
uorescence, equivalent to sequestration of 0.2-0.5 mu M cytosolic iron
, depending on the degree of pre-exposure to Tf, Addition of iron(III)
chelators to permeabilized 2,2'-bipyridyl-treated cells, failed to re
veal significant levels of chelatable iron(III), The finding that the
bulk of the in situ cell chelatable pool is comprised of iron(II) was
corroborated by pulsing K562 cells with Tf-Fe-55, followed by addition
of iron(II) and/or iron(III) chelators and extraction of chelator-Fe-
55 complexes into organic solvent. Virtually all of the accumulated Fe
-55 in the chelatable pool could be complexed by iron(II) chelators, T
he cytoplasmic concentration of iron(II) fluctuated between 0.3 and 0.
5 mu M, and its mean transit time through the chelatable pool was 1-2
h, me conclude that after iron is translocated from the endosomes, it
is maintained in the cytosol as a transit pool of chelatable iron(II),
The ostensible absence of chelatable iron(III) implicates the intrace
llular operation of vigorous reductive mechanisms.