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转铁蛋白和 H 铁蛋白在出生后发育过程中脑铁摄取中的作用:性别和基因型的影响。

Transferrin and H-ferritin involvement in brain iron acquisition during postnatal development: impact of sex and genotype.

机构信息

Department of Neurosurgery, Penn State College of Medicine, Hershey, Pennsylvania, USA.

Department of Neural and Behavioral Sciences, Penn State College of Medicine, Hershey, Pennsylvania, USA.

出版信息

J Neurochem. 2020 Feb;152(3):381-396. doi: 10.1111/jnc.14834. Epub 2019 Aug 22.

Abstract

Iron delivery to the developing brain is essential for energy and metabolic support needed for processes such as myelination and neuronal development. Iron deficiency, especially in the developing brain, can result in a number of long-term neurological deficits that persist into adulthood. There is considerable debate that excess access to iron during development may result in iron overload in the brain and subsequently predispose individuals to age-related neurodegenerative diseases. There is a significant gap in knowledge regarding how the brain acquires iron during development and how biological variables such as development, genetics, and sex impact brain iron status. In this study, we used a mouse model expressing a mutant form of the iron homeostatic regulator protein HFE, (Hfe H63D), the most common gene variant in Caucasians, to determine impact of the mutation on brain iron uptake. Iron uptake was assessed using Fe bound to either transferrin or H-ferritin as the iron carrier proteins. We demonstrate that at postnatal day 22, mutant mice brains take up greater amounts of iron compared with wildtype. Moreover, we introduce H-ferritin as a key protein in brain iron transport during development and identify a sex and genotype effect demonstrating female mutant mice take up more iron by transferrin, whereas male mutant mice take up more iron from H-ferritin at PND22. Furthermore, we begin to elucidate the mechanism for uptake using immunohistochemistry to profile the regional distribution and temporal expression of transferrin receptor and T-cell immunoglobulin and mucin domain 2, the latter is the receptor for H-ferritin. These data demonstrate that sex and genotype have significant effects on iron uptake and that regional receptor expression may play a large role in the uptake patterns during development. Open Science: This manuscript was awarded with the Open Materials Badge For more information see: https://cos.io/our-services/open-science-badges/ Cover Image for this issue: doi: 10.1111/jnc.14731.

摘要

铁向发育中的大脑的输送对于髓鞘形成和神经元发育等过程所需的能量和代谢支持至关重要。铁缺乏,尤其是在发育中的大脑中,会导致许多长期的神经缺陷,这些缺陷会持续到成年期。有相当多的争论认为,在发育过程中过度获取铁可能导致大脑中铁过载,随后使个体易患与年龄相关的神经退行性疾病。关于大脑在发育过程中如何获取铁以及发育、遗传和性别等生物变量如何影响大脑铁状态,人们的知识还存在很大差距。在这项研究中,我们使用了一种表达铁稳态调节剂蛋白 HFE 的突变形式(Hfe H63D)的小鼠模型,这是白种人中最常见的基因变体,以确定该突变对大脑铁摄取的影响。铁摄取通过使用与转铁蛋白或 H-铁蛋白结合的 Fe 作为铁载体蛋白来评估。我们证明,在出生后第 22 天,突变小鼠的大脑摄取的铁比野生型更多。此外,我们引入 H-铁蛋白作为发育过程中大脑铁转运的关键蛋白,并发现性别和基因型的影响,表明雌性突变小鼠通过转铁蛋白摄取更多的铁,而雄性突变小鼠在 PND22 时从 H-铁蛋白摄取更多的铁。此外,我们开始通过免疫组织化学来阐明摄取的机制,以描绘转铁蛋白受体和 T 细胞免疫球蛋白和粘蛋白结构域 2 的区域分布和时间表达,后者是 H-铁蛋白的受体。这些数据表明,性别和基因型对铁摄取有显著影响,而区域受体表达可能在发育过程中的摄取模式中起重要作用。开放科学:本文获得了开放材料徽章。更多信息请见:https://cos.io/our-services/open-science-badges/本期的封面图片:doi: 10.1111/jnc.14731.

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