Lin Lan, Valore Erika V, Nemeth Elizabeta, Goodnough Julia B, Gabayan Victoria, Ganz Tomas
Departments of Pathology, David Geffen School of Medicine, University of California, Los Angeles, CA 90095-1690, USA.
Blood. 2007 Sep 15;110(6):2182-9. doi: 10.1182/blood-2007-04-087593. Epub 2007 May 31.
The peptide hormone hepcidin is the principal regulator of systemic iron homeostasis. We examined the pathway by which iron stimulates the production of hepcidin. In humans who ingested 65 mg of iron, the increase in transferrin saturation preceded by hours the increase in urinary hepcidin excretion. Increases in urinary hepcidin concentrations were proportional to the increment in transferrin saturation. Paradoxically, in previous studies in primary hepatocytes and cell lines, hepcidin response to iron or iron transferrin was not observed. We now report that freshly isolated murine primary hepatocytes responded to holotransferrin but not apotransferrin by increasing hepcidin mRNA. Hepcidin increase was not due to contamination of the transferrin preparations by endotoxin, a potent pathologic stimulus of hepcidin synthesis. Using this culture system, we showed that holotransferrin concentrations regulate hepcidin mRNA concentrations through a hemojuvelin/BMP2/4-dependent pathway. Although BMP9 is known to be expressed in the liver and potently increased the basal concentrations of hepcidin mRNA, it did not interact with hemojuvelin, and interference with its signaling pathway did not affect iron regulation. Fresh primary hepatocytes constitute a sufficient system for the regulation of hepcidin by physiologic iron stimuli and will greatly facilitate studies of major disorders of iron homeostasis.
肽激素铁调素是全身铁稳态的主要调节因子。我们研究了铁刺激铁调素产生的途径。在摄入65毫克铁的人类中,转铁蛋白饱和度的增加比尿铁调素排泄量的增加提前数小时。尿铁调素浓度的增加与转铁蛋白饱和度的增加成正比。矛盾的是,在先前对原代肝细胞和细胞系的研究中,未观察到铁调素对铁或转铁蛋白铁的反应。我们现在报告,新鲜分离的小鼠原代肝细胞通过增加铁调素mRNA对全转铁蛋白而非脱铁转铁蛋白作出反应。铁调素的增加并非由于转铁蛋白制剂被内毒素污染所致,内毒素是铁调素合成的一种强效病理刺激物。利用该培养系统,我们表明全转铁蛋白浓度通过血色素沉着症相关蛋白/骨形态发生蛋白2/4依赖性途径调节铁调素mRNA浓度。尽管已知骨形态发生蛋白9在肝脏中表达并能有效增加铁调素mRNA的基础浓度,但它不与血色素沉着症相关蛋白相互作用,并且干扰其信号通路并不影响铁的调节。新鲜原代肝细胞构成了一个足够的系统,用于生理铁刺激对铁调素的调节,并将极大地促进对铁稳态主要紊乱的研究。