Chua Anita C G, Drake Sarah F, Herbison Carly E, Olynyk John K, Leedman Peter J, Trinder Debbie
School of Medicine and Pharmacology, Fremantle Hospital, The University of Western Australia, Fremantle, WA 6160, Australia.
J Hepatol. 2006 Jan;44(1):176-82. doi: 10.1016/j.jhep.2005.08.012. Epub 2005 Sep 19.
BACKGROUND/AIMS: In hereditary hemochromatosis, iron-loading of hepatocytes is associated with increased iron uptake while little is known about iron release. This study aims to characterise iron release and ferroportin expression by Hfe knockout hepatocytes to determine if they contribute to iron overload in haemochromatosis.
Iron release by hepatocytes from Hfe knockout, non-iron-loaded and iron-loaded wild-type mice was measured after incubation with nontransferrin-bound iron as iron-citrate.
Iron release and ferroportin expression by hepatocytes from Hfe knockout, non-iron-loaded and in vivo iron-loaded wild-type mice were similar although, nontransferrin-bound iron uptake was significantly increased in Hfe knockout hepatocytes and decreased in iron-loaded wild-type hepatocytes compared with non-iron-loaded wild-type cells. When expressed as a percentage of total iron uptake, iron release was decreased in Hfe knockout hepatocytes (4.6+/-0.7 versus 13.7+/-1.2%, P<0.0001) and increased in iron-loaded wild-type hepatocytes (29.5+/-0.5 versus 13.5+/-0.7%; P<0.0001) compared with wild-type hepatocytes. In contrast, in vitro iron-loading increased iron release and ferroportin expression by both Hfe knockout and wild-type hepatocytes.
Hfe knockout hepatocytes accumulate iron as a result of limited iron export and enhanced iron uptake. The correlation between iron release and ferroportin expression suggests that iron export in hepatocytes is mediated by ferroportin.
背景/目的:在遗传性血色素沉着症中,肝细胞的铁负荷与铁摄取增加有关,而关于铁释放的情况却知之甚少。本研究旨在对Hfe基因敲除肝细胞的铁释放和铁转运蛋白表达进行表征,以确定它们是否导致血色素沉着症中的铁过载。
用柠檬酸铁作为非转铁蛋白结合铁孵育后,测量来自Hfe基因敲除、未铁负荷和铁负荷野生型小鼠的肝细胞的铁释放。
来自Hfe基因敲除、未铁负荷和体内铁负荷野生型小鼠的肝细胞的铁释放和铁转运蛋白表达相似,尽管与未铁负荷的野生型细胞相比,Hfe基因敲除肝细胞中的非转铁蛋白结合铁摄取显著增加,而铁负荷野生型肝细胞中的非转铁蛋白结合铁摄取减少。当以总铁摄取的百分比表示时,与野生型肝细胞相比,Hfe基因敲除肝细胞中的铁释放减少(4.6±0.7对13.7±1.2%,P<0.0001),而铁负荷野生型肝细胞中的铁释放增加(29.5±0.5对13.5±0.7%;P<0.0001)。相反,体外铁负荷增加了Hfe基因敲除和野生型肝细胞的铁释放和铁转运蛋白表达。
Hfe基因敲除肝细胞由于铁输出受限和铁摄取增强而积累铁。铁释放与铁转运蛋白表达之间的相关性表明,肝细胞中的铁输出由铁转运蛋白介导。