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Blood, 15 May 2004, Vol. 103, No. 10, pp. 3933-3939.
Prepublished online as a Blood First Edition Paper on January 29, 2004; DOI 10.1182/blood-2003-09-3139.

Submitted September 15, 2003
Accepted January 16, 2004
Hephaestin is a ferroxidase that maintains partial activity in sex linked anemia mice
Huijun Chen, Zouhair K Attieh, Trent Su, Basharut A Syed, Hua Gao, Rima M Alaeddine, Tama C Fox, Julnar Usta, Claire E Naylor, Robert W Evans, Andrew T McKie, Gregory J Anderson, and Chris D Vulpe*
Nutritional Sciences and Toxicology, University of California, Berkeley, Berkeley, CA, USA
Nutritional Sciences and Toxicology, University of California, Berkeley, Berkeley, CA, USA; Department of Health Sciences, The American University of Science and Technology, Beirut, Lebanon
Nutritional Sciences and Toxicology, University of California, Berkeley, Berkeley, CA, USA; Metalloprotein Research Group, King's College London, London, United Kingdom
Department of Biochemistry, The American University of Beirut, Beirut, Lebanon
Department of Crystallography, Birkbeck College, London, United Kingdom
Metalloprotein Research Group, King's College London, London, United Kingdom
Department of Molecular Medicine, King's College London, London, United Kingdom
The Queensland Institute of Medical Research, University of Queensland, Brisbane, Queensland, Australia
* Corresponding author; email: vulpe{at}uclink4.berkeley.edu.
Hephaestin (Hp) plays an important role in intestinal iron absorption and is predicted to be a ferroxidase based on significant sequence identity to the serum multi-copper ferroxidase ceruloplasmin. Here, we demonstrate that Hp has both amine oxidase and ferroxidase activity in cultured cells and primary intestinal enterocytes using both gel and solution assays. The specificity of the activity is shown by immuno-blotting, immuno-precipitation and immuno-depletion experiments. Surprisingly, the truncated hephaestin expressed in sla mice still has measurable, but decreased, oxidase activity. Molecular modeling of the truncated hephaestin suggests retention of a minimum catalytic core required for enzymatic activity. We suggest that hephaestin, via its ferroxidase activity, facilitates iron export from intestinal enterocytes, most likely in cooperation with the basolateral iron transporter, Ireg1.

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