• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

铁转运蛋白:细胞和全身铁稳态的通道

Iron transport proteins: Gateways of cellular and systemic iron homeostasis.

作者信息

Knutson Mitchell D

机构信息

Food Science and Human Nutrition Department, University of Florida, Gainesville, Florida 32611-03170.

出版信息

J Biol Chem. 2017 Aug 4;292(31):12735-12743. doi: 10.1074/jbc.R117.786632. Epub 2017 Jun 14.

DOI:10.1074/jbc.R117.786632
PMID:28615441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5546014/
Abstract

Cellular iron homeostasis is maintained by iron and heme transport proteins that work in concert with ferrireductases, ferroxidases, and chaperones to direct the movement of iron into, within, and out of cells. Systemic iron homeostasis is regulated by the liver-derived peptide hormone, hepcidin. The interface between cellular and systemic iron homeostasis is readily observed in the highly dynamic iron handling of four main cell types: duodenal enterocytes, erythrocyte precursors, macrophages, and hepatocytes. This review provides an overview of how these cell types handle iron, highlighting how iron and heme transporters mediate the exchange and distribution of body iron in health and disease.

摘要

细胞铁稳态由铁和血红素转运蛋白维持,这些蛋白与铁还原酶、铁氧化酶和伴侣蛋白协同作用,以指导铁进出细胞以及在细胞内的移动。系统性铁稳态由肝脏衍生的肽激素铁调素调节。在四种主要细胞类型(十二指肠肠上皮细胞、红细胞前体、巨噬细胞和肝细胞)高度动态的铁处理过程中,很容易观察到细胞和系统性铁稳态之间的相互作用。本综述概述了这些细胞类型如何处理铁,重点介绍了铁和血红素转运蛋白在健康和疾病状态下如何介导体内铁的交换和分布。

相似文献

1
Iron transport proteins: Gateways of cellular and systemic iron homeostasis.铁转运蛋白:细胞和全身铁稳态的通道
J Biol Chem. 2017 Aug 4;292(31):12735-12743. doi: 10.1074/jbc.R117.786632. Epub 2017 Jun 14.
2
Iron homeostasis: An anthropocentric perspective.铁稳态:以人类为中心的视角
J Biol Chem. 2017 Aug 4;292(31):12727-12734. doi: 10.1074/jbc.R117.781823. Epub 2017 Jun 14.
3
Intestinal expression of genes implicated in iron absorption and their regulation by hepcidin.肠内铁吸收相关基因的表达及其受铁调素的调控。
Clin Nutr. 2017 Oct;36(5):1427-1433. doi: 10.1016/j.clnu.2016.09.021. Epub 2016 Sep 30.
4
Mechanistic and regulatory aspects of intestinal iron absorption.肠道铁吸收的机制和调节方面。
Am J Physiol Gastrointest Liver Physiol. 2014 Aug 15;307(4):G397-409. doi: 10.1152/ajpgi.00348.2013. Epub 2014 Jul 3.
5
Molecular basis of hereditary iron homeostasis defects.遗传性铁稳态缺陷的分子基础。
Hematology. 2010 Apr;15(2):96-111. doi: 10.1179/102453310X12583347009810.
6
Iron metabolism: State of the art.铁代谢:最新进展
Transfus Clin Biol. 2017 Sep;24(3):115-119. doi: 10.1016/j.tracli.2017.06.015. Epub 2017 Jul 8.
7
Comparative studies of duodenal and macrophage ferroportin proteins.十二指肠和巨噬细胞铁转运蛋白的比较研究。
Am J Physiol Gastrointest Liver Physiol. 2006 Jan;290(1):G156-63. doi: 10.1152/ajpgi.00227.2005. Epub 2005 Aug 4.
8
Iron homeostasis: transport, metabolism, and regulation.铁稳态:转运、代谢与调节
Curr Opin Clin Nutr Metab Care. 2016 Jul;19(4):276-81. doi: 10.1097/MCO.0000000000000285.
9
[Erythrophagocytosis and recycling of heme iron in normal and pathological conditions; regulation by hepcidin].[正常及病理状态下的红细胞吞噬作用与血红素铁的再循环;铁调素的调节作用]
Transfus Clin Biol. 2005 Jun;12(2):123-30. doi: 10.1016/j.tracli.2005.04.017.
10
Molecular mediators governing iron-copper interactions.调控铁-铜相互作用的分子介质。
Annu Rev Nutr. 2014;34:95-116. doi: 10.1146/annurev-nutr-071812-161215. Epub 2014 Jun 2.

引用本文的文献

1
Iron-Inflammasome Crosstalk in Adipose Tissue: Unresolved Roles of NLRP3 and IL-1β in Metabolic Inflammation.脂肪组织中的铁-炎性小体相互作用:NLRP3和IL-1β在代谢性炎症中尚未明确的作用
Int J Mol Sci. 2025 Aug 27;26(17):8304. doi: 10.3390/ijms26178304.
2
Biomarkers of Metabolism and Inflammation in Individuals with Obesity and Normal Weight: A Comparative Analysis Exploring Sex Differences.肥胖与正常体重个体的代谢和炎症生物标志物:一项探索性别差异的比较分析
Int J Mol Sci. 2025 Aug 5;26(15):7576. doi: 10.3390/ijms26157576.
3
Autologous and synthetic vascular grafts trigger different host responses in the anastomotic regions and in the perivascular adipose tissue during the early healing phase.在早期愈合阶段,自体血管移植物和合成血管移植物在吻合区域和血管周围脂肪组织中引发不同的宿主反应。
Mater Today Bio. 2025 Jul 15;33:102089. doi: 10.1016/j.mtbio.2025.102089. eCollection 2025 Aug.
4
Integrative computational approaches identify haptoglobin inhibitors to modulate erythrocyte sedimentation rate in trauma-linked inflammatory and haematological malignancies.综合计算方法鉴定触珠蛋白抑制剂以调节创伤相关炎症和血液系统恶性肿瘤中的红细胞沉降率。
Front Chem. 2025 Jun 18;13:1611972. doi: 10.3389/fchem.2025.1611972. eCollection 2025.
5
Plant-Based Diet and Risk of Iron-deficiency Anemia. A Review of the Current Evidence and Implications for Preventive Strategies.植物性饮食与缺铁性贫血风险。当前证据综述及对预防策略的启示
Curr Nutr Rep. 2025 Jun 18;14(1):81. doi: 10.1007/s13668-025-00671-y.
6
Effects of iron accumulation and its chelation on oxidative stress in intracortical implants.铁蓄积及其螯合对皮质内植入物氧化应激的影响。
Acta Biomater. 2025 Jun 15;200:703-723. doi: 10.1016/j.actbio.2025.05.026. Epub 2025 May 10.
7
Review of the anatomical basis for predicting plutonium alpha particle radiation induced osteogenic cancers.预测钚α粒子辐射诱发成骨肉瘤的解剖学基础综述。
Anat Rec (Hoboken). 2025 Feb 18. doi: 10.1002/ar.25641.
8
Ferroptosis in senescence and age-related diseases: pathogenic mechanisms and potential intervention targets.衰老及年龄相关疾病中的铁死亡:致病机制与潜在干预靶点
Mol Biol Rep. 2025 Feb 17;52(1):238. doi: 10.1007/s11033-025-10338-0.
9
In vitro reconstitution of transition metal transporters.体外重建过渡金属转运蛋白。
J Biol Chem. 2024 Aug;300(8):107589. doi: 10.1016/j.jbc.2024.107589. Epub 2024 Jul 19.
10
Interfaces between Cranial Bone and AISI 304 Steel after Long-Term Implantation: A Case Study of Cranial Screws.颅骨与 AISI 304 钢长期植入后的界面:颅骨螺钉的案例研究。
ACS Biomater Sci Eng. 2024 Jul 8;10(7):4297-4310. doi: 10.1021/acsbiomaterials.4c00309. Epub 2024 Jun 20.

本文引用的文献

1
Regulation of the Iron Homeostatic Hormone Hepcidin.铁稳态激素铁调素的调节
Adv Nutr. 2017 Jan 17;8(1):126-136. doi: 10.3945/an.116.013961. Print 2017 Jan.
2
Endothelial cells produce bone morphogenetic protein 6 required for iron homeostasis in mice.内皮细胞产生小鼠铁稳态所需的骨形态发生蛋白6。
Blood. 2017 Jan 26;129(4):405-414. doi: 10.1182/blood-2016-06-721571. Epub 2016 Nov 18.
3
Intestinal brush-border Na+/H+ exchanger-3 drives H+-coupled iron absorption in the mouse.肠道刷状缘钠/氢交换蛋白3驱动小鼠体内氢离子偶联的铁吸收。
Am J Physiol Gastrointest Liver Physiol. 2016 Sep 1;311(3):G423-30. doi: 10.1152/ajpgi.00167.2016. Epub 2016 Jul 7.
4
Iron Export through the Transporter Ferroportin 1 Is Modulated by the Iron Chaperone PCBP2.通过转运蛋白铁转运蛋白1的铁输出受铁伴侣蛋白PCBP2调节。
J Biol Chem. 2016 Aug 12;291(33):17303-18. doi: 10.1074/jbc.M116.721936. Epub 2016 Jun 14.
5
Intestinal DMT1 is critical for iron absorption in the mouse but is not required for the absorption of copper or manganese.肠道二价金属离子转运体1对小鼠铁吸收至关重要,但对铜或锰的吸收并非必需。
Am J Physiol Gastrointest Liver Physiol. 2015 Oct 15;309(8):G635-47. doi: 10.1152/ajpgi.00160.2015. Epub 2015 Aug 20.
6
SLC39A14 Is Required for the Development of Hepatocellular Iron Overload in Murine Models of Hereditary Hemochromatosis.SLC39A14是遗传性血色素沉着症小鼠模型中肝细胞铁过载发展所必需的。
Cell Metab. 2015 Jul 7;22(1):138-50. doi: 10.1016/j.cmet.2015.05.002. Epub 2015 May 28.
7
Mice are poor heme absorbers and do not require intestinal Hmox1 for dietary heme iron assimilation.小鼠对血红素的吸收能力较差,并且在饮食血红素铁同化过程中不需要肠道血红素加氧酶1。
Haematologica. 2015 Sep;100(9):e334-7. doi: 10.3324/haematol.2015.126870. Epub 2015 May 14.
8
Prion protein functions as a ferrireductase partner for ZIP14 and DMT1.朊病毒蛋白作为ZIP14和DMT1的铁还原酶伴侣发挥作用。
Free Radic Biol Med. 2015 Jul;84:322-330. doi: 10.1016/j.freeradbiomed.2015.03.037. Epub 2015 Apr 8.
9
Macrophages and iron trafficking at the birth and death of red cells.红细胞生成与死亡过程中的巨噬细胞及铁转运
Blood. 2015 May 7;125(19):2893-7. doi: 10.1182/blood-2014-12-567776. Epub 2015 Mar 16.
10
Meta-analysis of the turnover of intestinal epithelia in preclinical animal species and humans.临床前动物物种和人类肠道上皮细胞更新的荟萃分析。
Drug Metab Dispos. 2014 Dec;42(12):2016-22. doi: 10.1124/dmd.114.058404. Epub 2014 Sep 18.