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Iron and Zinc Homeostasis and Interactions: Does Enteric Zinc Excretion Cross-Talk with Intestinal Iron Absorption?

机译:铁和锌的稳态和相互作用:肠内锌的排泄与肠道铁的吸收是否相互影响?

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摘要

Iron and zinc are essential micronutrients required for growth and health. Deficiencies of these nutrients are highly prevalent among populations, but can be alleviated by supplementation and food fortification. Cross-sectional studies in humans showed positive association of serum zinc levels with hemoglobin and markers of iron status. Dietary restriction of zinc or intestinal specific conditional knock out of ZIP4 (SLC39A4), an intestinal zinc transporter, in experimental animals demonstrated iron deficiency anemia and tissue iron accumulation. Similarly, increased iron accumulation has been observed in cultured cells exposed to zinc deficient media. These results together suggest a potential role of zinc in modulating intestinal iron absorption and mobilization from tissues. Studies in intestinal cell culture models demonstrate that zinc induces iron uptake and transcellular transport via induction of divalent metal iron transporter-1 (DMT1) and ferroportin (FPN1) expression, respectively. It is interesting to note that intestinal cells are exposed to very high levels of zinc through pancreatic secretions, which is a major route of zinc excretion from the body. Therefore, zinc appears to be modulating the iron metabolism possibly via regulating the DMT1 and FPN1 levels. Herein we critically reviewed the available evidence to hypothesize novel mechanism of Zinc-DMT1/FPN1 axis in regulating intestinal iron absorption and tissue iron accumulation to facilitate future research aimed at understanding the yet elusive mechanisms of iron and zinc interactions.
机译:铁和锌是生长和健康所需的必需微量营养素。这些营养素的缺乏在人群中非常普遍,但是可以通过补充和强化食物来缓解。对人体的横断面研究表明,血清锌水平与血红蛋白和铁状态标志呈正相关。锌的饮食限制或肠道锌转运蛋白ZIP4(SLC39A4)的肠道特异性条件性敲除试验动物表现出铁缺乏性贫血和组织铁蓄积。类似地,在暴露于缺锌培养基的培养细胞中观察到铁积累增加。这些结果共同表明锌在调节肠道铁从组织的吸收和动员中的潜在作用。肠道细胞培养模型的研究表明,锌分别通过诱导二价金属铁转运蛋白1(DMT1)和铁转运蛋白(FPN1)的表达来诱导铁吸收和跨细胞转运。有趣的是,肠道细胞通过胰腺分泌物暴露于很高水平的锌中,这是锌从体内排泄的主要途径。因此,锌可能通过调节DMT1和FPN1的水平来调节铁的代谢。在这里,我们批判性地审查了可用的证据来假设Zinc-DMT1 / FPN1轴在调节肠道铁吸收和组织铁积累中的新机制,以促进旨在了解铁和锌相互作用的尚未阐明的机制的未来研究。

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