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Mutations in the HFE / Hfe gene cause Hereditary Hemochromatosis (HH), a highly prevalent genetic disorder characterized by elevated iron deposition in multiple tissues. HFE acts in hepatocytes to control hepcidin expression, whereas HFE actions in myeloid cells are required for cell-autonomous and systemic iron regulation in aged mice. To address the role of HFE specifically in liver-resident macrophages, we generated mice with a selective Hfe deficiency in Kupffer cells ( Hfe  Clec4fCre ). The analysis of the major iron parameters in this novel Hfe Clec4fCre  mouse model led us to the conclusion that HFE actions in Kupffer cells are largely dispensable for cellular, hepatic and systemic iron homeostasis.

Hfe Actions in Kupffer Cells Are Dispensable for Hepatic and Systemic Iron Metabolism