During the absorption of dietary nonheme iron in the proximal small intestine, iron traverses the enterocyte cytosol, where it may be stored in ferritin complexes. NCOA4, a cargo receptor that promotes the autophagic degradation of ferritin, is expressed in enterocytes and is upregulated by HIF-2α. NCOA4 activity enhances iron uptake in the context of systemic iron overload, because loss of NCOA4 in enterocytes attenuates systemic iron loading in a mouse model of hemochromatosis caused by hepcidin gene disruption.

During the absorption of dietary nonheme iron in the proximal small intestine, iron traverses the enterocyte cytosol, where it may be stored in ferritin complexes. NCOA4, a cargo receptor that promotes the autophagic degradation of ferritin, is expressed in enterocytes and is upregulated by HIF-2α. NCOA4 activity enhances iron uptake in the context of systemic iron overload, because loss of NCOA4 in enterocytes attenuates systemic iron loading in a mouse model of hemochromatosis caused by hepcidin gene disruption.

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