Lady Davis Institute for Medical Research, Jewish General Hospital, and Department of Medicine, McGill University, Montreal, Quebec, Canada.
Department of Anatomy and Cell Biology, McGill University, Montreal, Quebec, Canada.
PLoS One. 2019 Aug 23;14(8):e0221455. doi: 10.1371/journal.pone.0221455. eCollection 2019.
Hepatic iron overload, a hallmark of hereditary hemochromatosis, triggers progressive liver disease. There is also increasing evidence for a pathogenic role of iron in non-alcoholic fatty liver disease (NAFLD), which may progress to non-alcoholic steatohepatitis (NASH), fibrosis, cirrhosis and hepatocellular cancer. Mouse models of hereditary hemochromatosis and NAFLD can be used to explore potential interactions between iron and lipid metabolic pathways. Hfe-/- mice, a model of moderate iron overload, were reported to develop early liver fibrosis in response to a high fat diet. However, this was not the case with Hjv-/- mice, a model of severe iron overload. These data raised the possibility that the Hfe gene may protect against liver injury independently of its iron regulatory function. Herein, we addressed this hypothesis in a comparative study utilizing wild type, Hfe-/-, Hjv-/- and double Hfe-/-Hjv-/- mice. The animals, all in C57BL/6J background, were fed with high fat diets for 14 weeks and developed hepatic steatosis, associated with iron overload. Hfe co-ablation did not sensitize steatotic Hjv-deficient mice to liver injury. Moreover, we did not observe any signs of liver inflammation or fibrosis even in single steatotic Hfe-/- mice. Ultrastructural studies revealed a reduced lipid and glycogen content in Hjv-/- hepatocytes, indicative of a metabolic defect. Interestingly, glycogen levels were restored in double Hfe-/-Hjv-/- mice, which is consistent with a metabolic function of Hfe. We conclude that hepatocellular iron excess does not aggravate diet-induced steatosis to steatohepatitis or early liver fibrosis in mouse models of hereditary hemochromatosis, irrespectively of the presence or lack of Hfe.
肝脏铁过载是遗传性血色病的标志,可引发进行性肝病。越来越多的证据表明,铁在非酒精性脂肪性肝病(NAFLD)中具有致病作用,该病可能进展为非酒精性脂肪性肝炎(NASH)、纤维化、肝硬化和肝细胞癌。遗传性血色病和 NAFLD 的小鼠模型可用于探索铁和脂质代谢途径之间的潜在相互作用。Hfe-/- 小鼠是一种中度铁过载模型,据报道,其在高脂肪饮食的作用下会早期发生肝纤维化。然而,在 Hjv-/- 小鼠(一种严重铁过载模型)中并非如此。这些数据提出了这样一种可能性,即 Hfe 基因可能独立于其铁调节功能来保护肝脏免受损伤。在此,我们在一项利用野生型、Hfe-/-、Hjv-/-和双 Hfe-/-Hjv-/- 小鼠的比较研究中探讨了这一假设。这些动物均为 C57BL/6J 背景,用高脂肪饮食喂养 14 周,发展为肝脂肪变性,并伴有铁过载。Hfe 共缺失并未使脂肪变性的 Hjv 缺陷型小鼠对肝损伤敏感。此外,即使在单一致脂肪变性的 Hfe-/- 小鼠中,我们也未观察到任何肝脏炎症或纤维化的迹象。超微结构研究显示 Hjv-/- 肝细胞中的脂质和糖原含量减少,表明存在代谢缺陷。有趣的是,在双 Hfe-/-Hjv-/- 小鼠中,糖原水平得到恢复,这与 Hfe 的代谢功能一致。我们得出结论,在遗传性血色病的小鼠模型中,肝细胞铁过载不会加重饮食诱导的脂肪变性向脂肪性肝炎或早期肝纤维化发展,无论 Hfe 的存在与否。