Mouse HFE inhibits Tf-uptake and iron accumulation but induces Non-Transferrin Bound Iron (NTBI)-uptake in transformed mouse fibroblasts

Merav Gleit Kielmanowicz, Nihay Laham, John E. Coligan, François Lemonnier, Rachel Ehrlich

Research output: Contribution to journalArticlepeer-review

Abstract

Iron-uptake and storage are tightly regulated to guarantee sufficient iron for essential cellular processes and to prevent the production of damaging free radicals. A non-classical class I MHC molecule, the hemochromatosis factor (HFE), has been shown to regulate iron metabolism, potentially via its interaction with the transferrin receptor. Whereas, the effect of human HFE (hHFE) on transferrin/ transferrin receptor association, as well as on transferrin receptor recycling and the level of cellular iron pools in various cell lines was analyzed, very little is known about the mouse HFE (mHFE) protein. In the following study, our aim was to analyze in more detail the function of mHFE. Surprisingly, we observed that over-expression of mHFE, but not of hHFE, in a mouse transformed cell line, results in a most significant inhibition of transferrin-uptake which correlated with apoptotic cell death. mHFE inhibited transferrin-uptake immediately following transfection and this inhibition persisted in the surviving stable transfectants. Concomitantly, cellular iron derived from transferrin-iron uptake was dramatically limited. The activation of a non-transferrin bound iron-uptake pathway that functions in the stable mHFE-transfected clones could explain their normal growth curves and survival. The hypothesis that iron starvation can induce iron-uptake by a novel transferrin-independent pathway is discussed.

Original languageEnglish
Pages (from-to)105-114
Number of pages10
JournalJournal of Cellular Physiology
Volume202
Issue number1
DOIs
StatePublished - Jan 2005

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