Department of Pediatrics, School of Medicine, University of Minnesota, Minneapolis, Minnesota.
Department of Neuroscience, University of Minnesota, Minneapolis, Minnesota.
J Nutr. 2024 Jan;154(1):49-59. doi: 10.1016/j.tjnut.2023.11.007. Epub 2023 Nov 19.
Developing neurons have high thyroid hormone and iron requirements to support their metabolically demanding growth. Early-life iron and thyroid-hormone deficiencies are prevalent and often coexist, and each independently increases risk of permanently impaired neurobehavioral function in children. Early-life dietary iron deficiency reduces thyroid-hormone concentrations and impairs thyroid hormone-responsive gene expression in the neonatal rat brain, but it is unclear whether the effect is cell-intrinsic.
This study determined whether neuronal-specific iron deficiency alters thyroid hormone-regulated gene expression in developing neurons.
Iron deficiency was induced in primary mouse embryonic hippocampal neuron cultures with the iron chelator deferoxamine (DFO) beginning at 3 d in vitro (DIV). At 11DIV and 18DIV, thyroid hormone-regulated gene messenger ribonucleic acid (mRNA)concentrations indexing thyroid hormone homeostasis (Hairless, mu-crystallin, Type II deiodinase, solute carrier family member 1c1, and solute carrier family member 16a2) and neurodevelopment (neurogranin, Parvalbumin, and Krüppel-like factor 9) were quantified. To assess the effect of iron repletion, DFO was removed at 14DIV from a subset of DFO-treated cultures, and gene expression and adenosine 5'-triphosphate (ATP) concentrations were quantified at 21DIV.
At 11DIV and 18DIV, neuronal iron deficiency decreased neurogranin, Parvalbumin, and mu-crystallin, and by 18DIV, solute carrier family member 16a2, solute carrier family member 1c1, Type II deiodinase, and Hairless were increased, suggesting cellular sensing of a functionally abnormal thyroid hormone state. Dimensionality reduction with Principal component analysis reveals that thyroid hormone homeostatic genes strongly correlate with and predict iron status. Iron repletion from 14-21DIV did not restore ATP concentration, and Principal component analysis suggests that, after iron repletion, cultures maintain a gene expression signature indicative of previous iron deficiency.
These novel findings suggest there is an intracellular mechanism coordinating cellular iron/thyroid hormone activities. We speculate this is a part of the homeostatic response to acutely match neuronal energy production and growth signaling. However, the adaptation to iron deficiency may cause permanent deficits in thyroid hormone-dependent neurodevelopmental processes even after recovery from iron deficiency.
发育中的神经元需要大量的甲状腺激素和铁来支持其代谢活跃的生长。婴幼儿时期铁和甲状腺激素的缺乏很常见,而且往往同时存在,每一种情况都会独立增加儿童神经行为功能永久受损的风险。婴幼儿时期的饮食缺铁会降低甲状腺激素浓度,并损害新生大鼠大脑中甲状腺激素反应基因的表达,但目前尚不清楚这种影响是否是细胞内在的。
本研究旨在确定神经元特异性铁缺乏是否会改变发育中的神经元中甲状腺激素调节的基因表达。
用铁螯合剂去铁胺(DFO)从体外培养 3 天(DIV)开始诱导原代培养的小鼠胚胎海马神经元中的铁缺乏。在 11DIV 和 18DIV 时,用定量聚合酶链反应测定甲状腺激素稳态相关基因(无毛基因、mu-晶体蛋白、II 型脱碘酶、溶质载体家族成员 1c1 和溶质载体家族成员 16a2)和神经发育相关基因(神经颗粒蛋白、Parvalbumin 和 Krüppel 样因子 9)的信使核糖核酸(mRNA)浓度。为了评估铁补充的效果,从一部分 DFO 处理的培养物中在 14DIV 时去除 DFO,并在 21DIV 时测定基因表达和三磷酸腺苷(ATP)浓度。
在 11DIV 和 18DIV 时,神经元铁缺乏降低了神经颗粒蛋白、Parvalbumin 和 mu-晶体蛋白的表达,到 18DIV 时,溶质载体家族成员 16a2、溶质载体家族成员 1c1、II 型脱碘酶和无毛基因的表达增加,这表明细胞感知到甲状腺激素功能异常的状态。主成分分析的降维显示,甲状腺激素稳态基因与铁状态强烈相关并可预测铁状态。从 14-21DIV 补充铁并没有恢复 ATP 浓度,主成分分析表明,在补充铁后,培养物保持了先前铁缺乏的基因表达特征。
这些新发现表明,存在一种协调细胞内铁/甲状腺激素活动的机制。我们推测这是一种急性匹配神经元能量产生和生长信号的细胞内稳态反应的一部分。然而,对铁缺乏的适应可能会导致甲状腺激素依赖性神经发育过程的永久性缺陷,即使在缺铁恢复后也是如此。