DMT1型
铁转运蛋白
海西定
转铁蛋白受体
铁蛋白
内化
转铁蛋白
化学
血红蛋白
运输机
骨髓
生物化学
新陈代谢
脾脏
细胞生物学
红细胞
内分泌学
受体
贫血
内科学
生物
免疫学
医学
基因
作者
Anne‐Cathrine S. Vogt,Tasneem Arsiwala,Mona O. Mohsen,Monique Vogel,Vania Manolova,Martin F. Bachmann
摘要
Iron is a critical metal for several vital biological processes. Most of the body’s iron is bound to hemoglobin in erythrocytes. Iron from senescent red blood cells is recycled by macrophages in the spleen, liver and bone marrow. Dietary iron is taken up by the divalent metal transporter 1 (DMT1) in enterocytes and transported to portal blood via ferroportin (FPN), where it is bound to transferrin and taken up by hepatocytes, macrophages and bone marrow cells via transferrin receptor 1 (TfR1). While most of the physiologically active iron is bound hemoglobin, the major storage of most iron occurs in the liver in a ferritin-bound fashion. In response to an increased iron load, hepatocytes secrete the peptide hormone hepcidin, which binds to and induces internalization and degradation of the iron transporter FPN, thus controlling the amount of iron released from the cells into the blood. This review summarizes the key mechanisms and players involved in cellular and systemic iron regulation.
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