Iron Homeostasis in the Liver

被引:207
作者
Anderson, Erik R. [1 ]
Shah, Yatrik M. [1 ,2 ]
机构
[1] Univ Michigan, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Internal Med, Div Gastroenterol, Ann Arbor, MI 48109 USA
基金
美国国家卫生研究院;
关键词
TRANSFERRIN-BOUND IRON; PROTEASE MATRIPTASE-2 TMPRSS6; REGULATORY PEPTIDE HEPCIDIN; FERRITIN HEAVY-CHAIN; DOWN-REGULATION; MOLECULAR-BASIS; FATTY LIVER; MOUSE MODEL; HEREDITARY HEMOCHROMATOSIS; HEPATOCELLULAR-CARCINOMA;
D O I
10.1002/cphy.c120016
中图分类号
Q4 [生理学];
学科分类号
071003 [生理学];
摘要
Iron is an essential nutrient that is tightly regulated. A principal function of the liver is the regulation of iron homeostasis. The liver senses changes in systemic iron requirements and can regulate iron concentrations in a robust and rapid manner. The last 10 years have led to the discovery of several regulatory mechanisms in the liver that control the production of iron regulatory genes, storage capacity, and iron mobilization. Dysregulation of these functions leads to an imbalance of iron, which is the primary cause of iron-related disorders. Anemia and iron overload are two of the most prevalent disorders worldwide and affect over a billion people. Several mutations in liver-derived genes have been identified, demonstrating the central role of the liver in iron homeostasis. During conditions of excess iron, the liver increases iron storage and protects other tissues, namely, the heart and pancreas from iron-induced cellular damage. However, a chronic increase in liver iron stores results in excess reactive oxygen species production and liver injury. Excess liver iron is one of the major mechanisms leading to increased steatohepatitis, fibrosis, cirrhosis, and hepatocellular carcinoma. (C) 2013 American Physiological Society. Compr Physiol 3:315-330, 2013.
引用
收藏
页码:315 / 330
页数:16
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