Skip to main content
. Author manuscript; available in PMC: 2019 Mar 1.
Published in final edited form as: Metallomics. 2018 Feb 27;10(3):370–377. doi: 10.1039/c8mt00015h

Fig. 6.

Fig. 6

The ferroxidase-dependent step in mammalian iron trafficking: managing iron on the way out. Presented within the context of either an epithelial or endothelial cell (e.g. enterocyte or brain microcapillary), managing the efflux step relies on hephaestin (Hp) or ceruloplasmin (Cp) ferroxidation of the Fpn-trafficked Fe2+. In one model of this step, the Fe3+ product is channeled to a recipient ferric iron chelator, e.g. apo-transferrin (Tf) in an associative mechanism comparable to the fungal Fet, Ftr uptake pathway.