ZIP Proteins and Iron Metabolism

ZIP 蛋白质和铁代谢

• 批准号: 8141398
• 负责人: Mitchell D Knutson
• 金额: $ 33.55万
• 依托单位: UNIVERSITY OF FLORIDA
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-08-01 至 2013-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8141398
• 关键词: Affect; Age; Applications Grants; Applied Genetics; Bacteria; Binding; Biological Process; Cell Culture Techniques; Cell membrane; Cells; Collaborations; DNA; Data; Dependence; Deposition; Diet; Dietary Iron; Dioxygen; Disease; Drug or chemical Tissue Distribution; Electron Transport; Family; Family member; Genes; Health; Hemochromatosis; Hepatic; Homeostasis; Human; Human body; Individual; Integral Membrane Protein; Intestines; Ions; Iron; Iron Metabolism Disorders; Iron Overload; Knock-out; Knockout Mice; Knowledge; Laboratories; Lead; Lipids; Liver; Measures; Mediating; Metabolism; Metals; Molecular; Morbidity - disease rate; Mus; Mutate; Nature; Nutrient; Organism; Oxidation-Reduction; Pathway interactions; Physiological; Play; Prevalence; Property; Proteins; Public Health; Radiolabeled; Rattus; Reaction; Reactive Oxygen Species; Regulation; Relative (related person); Research; Role; Techniques; Testing; Tissues; Transfection; Transferrin; Transition Elements; Up-Regulation; Venous blood sampling; Woman; Work; ZIP protein; Zinc; base; cell type; hazard; in vivo; iron metabolism; member; mortality; novel; overexpression; oxidation; protein transport; radiotracer; reproductive; research study; therapeutic target; trafficking; uptake; zinc-binding protein

DESCRIPTION (provided by applicant): Disturbances of iron metabolism increase morbidity and mortality and are among the most common disorders affecting humans. Nearly 20% of women of reproductive age in the US are iron deficient, and iron overload is increasingly being recognized as a public health concern. Despite the prevalence and adverse health effects associated with these disorders, many questions remain regarding the molecular mechanisms of iron transport. The long-term objective of the proposed work is to enhance our understanding of iron homeostasis by investigating the regulation and function of ZIP14 and other ZIP family members. ZIP14 was first identified as a zinc transporter, but recent studies indicate that it transports iron as well. Its abundant expression in the liver suggests that it plays a role in hepatic iron deposition during iron overload, and its upregulation in liver by phlebotomy and iron deficiency suggests that it functions in iron uptake. The first aim of the proposed research will be to investigate more completely the iron-dependent regulation of Zip14. Rats and mice will be made iron deficient, iron normal, or iron loaded, and a variety of tissues will be examined for Zip14 expression and cellular localization. In the second aim, cell culture studies will be used to identify the subcellular localization of Zip14 and to investigate its role in the uptake of transferrin-bound iron, the most common pathway of iron uptake by cells. To better define the in vivo role of Zip14, the third aim will characterize the iron status of Zip14 knockout mice. Tissue-specific knockout mice will be used to test the hypotheses that Zip14 plays a role in the uptake of non-transferrin-bound iron by the liver and dietary iron by the intestine. In the fourth aim, the iron transport activity of all mammalian ZIP proteins will be systematically assessed by overexpressing the proteins and measuring the uptake of radiolabeled iron. We will also examine the effect of in vivo iron status on the expression of all 14 ZIP family members. We anticipate that information derived from the experiments with Zip14, and perhaps other ZIP proteins, will be relevant to disorders of iron metabolism. Identification of other ZIP proteins that are capable of transporting iron or are regulated by iron status will enhance our basic understanding of iron homeostasis and metal ion trafficking in general. Disturbances of iron metabolism increase morbidity and mortality and are among the most common disorders affecting humans. Despite the prevalence and adverse health effects associated with these disorders, many questions remain regarding the molecular mechanisms of iron transport. The research described in this proposal will enhance our knowledge of iron transport, which will ultimately help to identify therapeutic targets for treating disorders of iron metabolism. PUBLIC HEALTH RELEVANCE: Disturbances of iron metabolism increase morbidity and mortality and are among the most common disorders affecting humans. Despite the prevalence and adverse health effects associated with these disorders, many questions remain regarding the molecular mechanisms of iron transport. The research described in this proposal will enhance our knowledge of iron transport, which will ultimately help to identify therapeutic targets for treating disorders of iron metabolism.

描述（由申请方提供）：铁代谢紊乱会增加发病率和死亡率，是影响人类的最常见疾病之一。在美国，近20%的育龄妇女缺铁，铁超载越来越被认为是一个公共卫生问题。尽管与这些疾病相关的患病率和不良健康影响，许多问题仍然存在关于铁转运的分子机制。这项工作的长期目标是通过研究ZIP14和其他ZIP家族成员的调节和功能来增强我们对铁稳态的理解。ZIP14最初被鉴定为锌转运蛋白，但最近的研究表明它也转运铁。其在肝脏中的丰富表达表明其在铁过载期间在肝铁沉积中起作用，并且其在静脉切开和铁缺乏时在肝脏中的上调表明其在铁摄取中起作用。这项研究的第一个目的是更全面地研究Zip14的铁依赖性调节。将使大鼠和小鼠缺铁、铁正常或铁负载，并检查各种组织的Zip 14表达和细胞定位。在第二个目标中，细胞培养研究将用于确定Zip14的亚细胞定位，并研究其在转铁蛋白结合铁（细胞摄取铁的最常见途径）摄取中的作用。为了更好地定义Zip14的体内作用，第三个目标将表征Zip14敲除小鼠的铁状态。组织特异性基因敲除小鼠将用于测试Zip14在肝脏摄取非转铁蛋白结合铁和肠道摄取膳食铁中发挥作用的假设。在第四个目标中，将通过过表达蛋白质和测量放射性标记的铁的摄取来系统地评估所有哺乳动物ZIP蛋白的铁转运活性。我们还将研究体内铁状态对所有14个ZIP家族成员表达的影响。我们预计，来自Zip14实验的信息，也许还有其他ZIP蛋白，将与铁代谢紊乱有关。其他ZIP蛋白，能够运输铁或铁的状态调节的鉴定将提高我们的铁稳态和金属离子贩运一般的基本理解。铁代谢紊乱增加发病率和死亡率，是影响人类的最常见疾病之一。尽管与这些疾病相关的患病率和不良健康影响，许多问题仍然存在关于铁转运的分子机制。本提案中描述的研究将增强我们对铁转运的了解，这将最终有助于确定治疗铁代谢紊乱的治疗靶点。公共卫生相关性：铁代谢紊乱会增加发病率和死亡率，是影响人类的最常见疾病之一。尽管与这些疾病相关的患病率和不良健康影响，许多问题仍然存在关于铁转运的分子机制。本提案中描述的研究将增强我们对铁转运的了解，这将最终有助于确定治疗铁代谢紊乱的治疗靶点。