1 Department of Neurosurgery, Penn State Hershey Medical Center, Hershey, PA, USA.
2 Department of Neural and Behavioral Sciences, Penn State Hershey Medical Center, Hershey, PA, USA.
J Cereb Blood Flow Metab. 2018 Mar;38(3):540-548. doi: 10.1177/0271678X17701949. Epub 2017 Mar 28.
HFE (high iron) is an essential protein for regulating iron transport into cells. Mutations of the HFE gene result in loss of this regulation causing accumulation of iron within the cell. The mutated protein has been found increasingly in numerous neurodegenerative disorders in which increased levels of iron in the brain are reported. Additionally, evidence that these mutations are associated with elevated brain iron challenges the paradigm that the brain is protected by the blood-brain barrier. While much has been studied regarding the role of HFE in cellular iron uptake, it has remained unclear what role the protein plays in the transport of iron into the brain. We investigated regulation of iron transport into the brain using a mouse model with a mutation in the HFE gene. We demonstrated that the rate of radiolabeled iron (Fe) uptake was similar between the two genotypes despite higher brain iron concentrations in the mutant. However, there were significant differences in iron uptake between males and females regardless of genotype. These data indicate that brain iron status is consistently maintained and tightly regulated at the level of the blood-brain barrier.
HFE(高铁)是一种调节铁向细胞内转运的必需蛋白。HFE 基因突变导致这种调节作用丧失,从而使细胞内铁蓄积。在许多神经退行性疾病中,越来越多地发现了这种突变蛋白,这些疾病报告称大脑中的铁含量增加。此外,这些突变与大脑铁含量升高相关的证据,对大脑受血脑屏障保护的这一观点提出了挑战。虽然人们已经对 HFE 在细胞铁摄取中的作用进行了大量研究,但仍不清楚该蛋白在铁向大脑转运中的作用。我们使用 HFE 基因突变的小鼠模型研究了铁向大脑的转运调节。我们证明,尽管突变体大脑中的铁浓度较高,但两种基因型之间放射性标记铁(Fe)摄取的速率相似。然而,无论基因型如何,雌雄两性之间的铁摄取都存在显著差异。这些数据表明,大脑铁状态在血脑屏障水平上始终保持一致并受到严格调节。